David A. Stevenson
Reproducibility track record
1
assessed papers
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mean reproducibility
0
reproduced (C1–C2)
0
flagged
0
total citations
flag rate:
0%
(0/1)
The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.
Authorship role
first author: 0
last author: 0
Topics
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Funders
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Frequent co-authors
Patroula Smpokou 1Verena Kolbe 1Georg Rosenberger 1Katia Sol‐Church 1David Viskochil 1Bridget Russo 1Deborah L. Stabley 1Nick Gardner 1Heather Hanson 1Karen W. Gripp 1
Institutions
Community Health Systems - Dupont Hospital 1Alfred I. duPont Hospital for Children 1Children's National 1Children's Hospital of Eastern Ontario 1Stanford University 1University of Utah 1
Geography (author institutions)
US 1CA 1DE 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (1)
Complete publication record (255)
Request a reproduction →1 assessed by us (0 reproduced) · 254 not yet assessed — every PubMed paper on record, linked below.
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<i>KMT2B</i>-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation. ↗PubMed · 2025 · PMID 39990802not yet assessed
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The American Federation for Medical Research maintains commitment to decades of support of vaccine and vaccination research to improve public health ↗Journal of Investigative Medicine · 2025 · PMID 40022538not yet assessed
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Medical genetics and genomics residency programs: Trends in applications, match rates, and matriculation from 2015 to 2024 ↗Genetics in Medicine · 2025 · PMID 41239884not yet assessed
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Guiding Parenteral Nutrition Therapy After Hematopoietic Stem Cell Transplantation ↗Research Square · 2025not yet assessed
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Risk of meningomyelocele mediated by the common 22q11.2 deletion ↗Science · 2024 · PMID 38696583not yet assessed
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Influences of RASopathies on Neuroanatomical Variation in Children ↗Biological Psychiatry Cognitive Neuroscience and Neuroimaging · 2024 · PMID 38621478not yet assessed
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Immunological and hematological findings as major features in a patient with a new germline pathogenic <scp> <i>CBL</i> </scp> variant ↗American Journal of Medical Genetics Part A · 2024 · PMID 38613168not yet assessed
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Osteogenesis imperfecta type XVII: expansion of the phenotype ↗Egyptian Journal of Medical Human Genetics · 2024not yet assessed
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7519 Withdrawal of DCCR (Diazoxide Choline) Extended-Release Tablets Worsens Hyperphagia and Increases Weight and BMI in a 16-week Double-blind, Placebo-controlled, Randomized Withdrawal Period in Patients with Prader Willi Syndrome ↗Journal of the Endocrine Society · 2024not yet assessed
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P857: Medical genetics and genomics residents’ perceptions of their gaps in knowledge regarding the clinical intersections of race and racism* ↗Genetics in Medicine Open · 2024not yet assessed
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Characterizing and Evaluating the Structures of Combined Pediatrics and Medical Genetics and Genomics Residency Programs ↗American Journal of Medical Genetics Part A · 2024 · PMID 39538988not yet assessed
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Diazoxide Choline Extended-Release Tablet in People With Prader-Willi Syndrome: A Double-Blind, Placebo-Controlled Trial ↗The Journal of Clinical Endocrinology & Metabolism · 2023 · PMID 36639249not yet assessed
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Diazoxide choline extended‐release tablet in people with <scp>Prader‐Willi</scp> syndrome: results from long‐term open‐label study ↗Obesity · 2023 · PMID 37919617not yet assessed
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Frequency of epistaxis and telangiectasia in patients with hereditary hemorrhagic telangiectasia (HHT) in comparison with the general population: Curaçao diagnostic criteria revisited ↗Genetics in Medicine · 2023 · PMID 37125633not yet assessed
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Two epilepsy‐associated variants in <i>KCNA2</i> (K<sub>V</sub>1.2) at position H310 oppositely affect channel functional expression ↗The Journal of Physiology · 2023 · PMID 37883018not yet assessed
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Single Versus Multigene Testing for Hereditary Hearing Loss: Use and Costs in a Commercially Insured Cohort ↗Otolaryngology · 2023 · PMID 36939467not yet assessed
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<scp>Jansen‐de Vries</scp> syndrome: Expansion of the <scp><i>PPM1D</i></scp> clinical and phenotypic spectrum in 34 families ↗American Journal of Medical Genetics Part A · 2023 · PMID 37183572not yet assessed
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Time to diagnosis in rapid exome/genome sequencing in the clinical inpatient setting ↗American Journal of Medical Genetics Part A · 2023 · PMID 38017634not yet assessed
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Papillomas of Costello syndrome are not associated with human papillomavirus infection in a small case series ↗Journal of the American Academy of Dermatology · 2023 · PMID 37028601not yet assessed
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Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome ↗American Journal of Medical Genetics Part A · 2023 · PMID 37675855not yet assessed
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Potential endpoints for assessment of bone health in persons with neurofibromatosis type 1 ↗Clinical Trials · 2023 · PMID 37772407not yet assessed
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Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation ↗Genetics in Medicine · 2022 · PMID 35674741not yet assessed
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MEK inhibitors for neurofibromatosis type 1 manifestations: Clinical evidence and consensus ↗Neuro-Oncology · 2022 · PMID 35788692not yet assessed
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The seventh international <scp>RASopathies</scp> symposium: Pathways to a cure—expanding knowledge, enhancing research, and therapeutic discovery ↗American Journal of Medical Genetics Part A · 2022 · PMID 35266292not yet assessed
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Evaluation of the impact of the 2021 revised Neurofibromatosis type 1 diagnostic criteria on time to diagnosis ↗American Journal of Medical Genetics Part A · 2022 · PMID 35779212not yet assessed
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Bone health in <scp>RASopathies</scp> ↗American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2022 · PMID 36461161not yet assessed
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Factors associated with the time to complete clinical exome sequencing in a pediatric patient population ↗Genetics in Medicine · 2022 · PMID 35951015not yet assessed
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A survey of program directors for combined pediatrics and medical genetics and genomics residency programs: Perspectives when evaluating applicants ↗American Journal of Medical Genetics Part A · 2022 · PMID 35633299not yet assessed
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50 Years Ago in T J P ↗The Journal of Pediatrics · 2022 · PMID 36058596not yet assessed
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Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation ↗Genetics in Medicine · 2021 · PMID 34012067not yet assessed
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A dyadic approach to the delineation of diagnostic entities in clinical genomics ↗The American Journal of Human Genetics · 2021 · PMID 33417889not yet assessed
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Arteriovenous Malformations—Current Understanding of the Pathogenesis with Implications for Treatment ↗International Journal of Molecular Sciences · 2021 · PMID 34445743not yet assessed
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Reliability of Handheld Dynamometry to Measure Focal Muscle Weakness in Neurofibromatosis Types 1 and 2 ↗Neurology · 2021 · PMID 34230196not yet assessed
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Natural history of NF1 c.2970_2972del p.(Met992del): confirmation of a low risk of complications in a longitudinal study ↗European Journal of Human Genetics · 2021 · PMID 34897289not yet assessed
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Congenital polyvalvular disease expands the cardiac phenotype of the <scp>RASopathies</scp> ↗American Journal of Medical Genetics Part A · 2021 · PMID 33683002not yet assessed
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Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma ↗Genetics in Medicine · 2021 · PMID 33879870not yet assessed
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Response to Hamosh et al. ↗The American Journal of Human Genetics · 2021 · PMID 34478656not yet assessed
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<i>KMT2B</i>-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation ↗Brain · 2020 · PMID 33150406not yet assessed
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Missense variants in <i>CTNNB1</i> can be associated with vitreoretinopathy—Seven new cases of <i>CTNNB1</i>‐associated neurodevelopmental disorder including a previously unreported retinal phenotype ↗Molecular Genetics & Genomic Medicine · 2020 · PMID 33350591not yet assessed
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Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome ↗Human Genetics and Genomics Advances · 2020 · PMID 33537682not yet assessed
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Are Some Randomized Clinical Trials Impossible? ↗Journal of Pediatric Orthopaedics · 2020 · PMID 32852366not yet assessed
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Costello syndrome: Clinical phenotype, genotype, and management guidelines ↗American Journal of Medical Genetics Part A · 2019 · PMID 31222966not yet assessed
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Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)? ↗Genetics in Medicine · 2019 · PMID 30760892not yet assessed
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Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review ↗American Journal of Medical Genetics Part A · 2019 · PMID 30920161not yet assessed
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Localization and age distribution of telangiectases in children and adolescents with hereditary hemorrhagic telangiectasia: A retrospective cohort study ↗Journal of the American Academy of Dermatology · 2019 · PMID 30819528not yet assessed
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NF1 Somatic Mutation in Dystrophic Scoliosis ↗Journal of Molecular Neuroscience · 2019 · PMID 30778836not yet assessed
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Capillary Malformation-Arteriovenous Malformation SyndromeEurope PMC (PubMed Central) · 2019not yet assessed
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Cardiac transplantation in children with Noonan syndrome ↗Pediatric Transplantation · 2019 · PMID 31259454not yet assessed
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Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) ↗Genetics in Medicine · 2018 · PMID 30006586not yet assessed
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Expanding the clinical and molecular findings in RASA1 capillary malformation-arteriovenous malformation ↗European Journal of Human Genetics · 2018 · PMID 29891884not yet assessed
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Contributing factors of mortality in Prader–Willi syndrome ↗American Journal of Medical Genetics Part A · 2018 · PMID 30569567not yet assessed
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PTPN11 Gain-of-Function Mutations Affect the Developing Human Brain, Memory, and Attention ↗Cerebral Cortex · 2018 · PMID 30059958not yet assessed
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Evaluation of racial disparities in pediatric optic pathway glioma incidence: Results from the Surveillance, Epidemiology, and End Results Program, 2000–2014 ↗Cancer Epidemiology · 2018 · PMID 29684801not yet assessed
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Proceedings of the fifth international RASopathies symposium: When development and cancer intersect ↗American Journal of Medical Genetics Part A · 2018 · PMID 30302932not yet assessed
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Predictive Value and Interrater Reliability of Radiographic Factors in Neurofibromatosis Patients With Dystrophic Scoliosis ↗Spine Deformity · 2018 · PMID 30122392not yet assessed
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Use of Flow Cytometry for Diagnosis of Epilepsy Associated With Homozygous PIGW Variants ↗Pediatric Neurology · 2018 · PMID 30078644not yet assessed
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Racial/ethnic disparities and incidence of malignant peripheral nerve sheath tumors: results from the Surveillance, Epidemiology, and End Results Program, 2000–2014 ↗Journal of Neuro-Oncology · 2018 · PMID 29663170not yet assessed
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A case report of a suspected dual diagnosis: 22q11.2 deletion syndrome and X-linked chondrodysplasia punctata ↗Clinical Dysmorphology · 2018 · PMID 29912012not yet assessed
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Response to Hannah-Shmouni and Stratakis ↗Genetics in Medicine · 2018 · PMID 30283095not yet assessed
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Neurofibromatosis Type 1 and Polydactyly ↗Case Reports in Orthopedic Research · 2018not yet assessed
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Gefitinib and <i>EGFR</i> Gene Copy Number Aberrations in Esophageal Cancer ↗Journal of Clinical Oncology · 2017 · PMID 28537764not yet assessed
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Evaluation of NGS and RT-PCR Methods for ALK Rearrangement in European NSCLC Patients: Results from the European Thoracic Oncology Platform Lungscape Project ↗Journal of Thoracic Oncology · 2017 · PMID 29191776not yet assessed
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Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders ↗Genome Medicine · 2017 · PMID 28807008not yet assessed
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Molecular and clinical spectra of FBXL4 deficiency ↗Human Mutation · 2017 · PMID 28940506not yet assessed
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Dietary intervention rescues myopathy associated with neurofibromatosis type 1 ↗Human Molecular Genetics · 2017 · PMID 29228356not yet assessed
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Promoting appropriate genetic testing: the impact of a combined test review and consultative service ↗Genetics in Medicine · 2017 · PMID 28125079not yet assessed
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Epistaxis in children and adolescents with hereditary hemorrhagic telangiectasia ↗The Laryngoscope · 2017 · PMID 29171658not yet assessed
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Variable clinical course of identical twin neonates with Alström syndrome presenting coincidentally with dilated cardiomyopathy ↗American Journal of Medical Genetics Part A · 2017 · PMID 28407410not yet assessed
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Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial Pseudarthrosis ↗Journal of Molecular Diagnostics · 2017 · PMID 28433079not yet assessed
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Quantitative Ultrasound and Tibial Dysplasia in Neurofibromatosis Type 1 ↗Journal of Clinical Densitometry · 2017 · PMID 28438404not yet assessed
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The path forward: 2015 International Children's Tumor Foundation conference on neurofibromatosis type 1, type 2, and schwannomatosisAuthor eBooks · 2017not yet assessed
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DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome ↗The American Journal of Human Genetics · 2016 · PMID 27569549not yet assessed
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<i>RASA1</i> somatic mutation and variable expressivity in capillary malformation/arteriovenous malformation (CM/AVM) syndrome ↗American Journal of Medical Genetics Part A · 2016 · PMID 26969842not yet assessed
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NALCN channelopathies ↗Neurology · 2016 · PMID 27558372not yet assessed
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The Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathway ↗American Journal of Medical Genetics Part A · 2016 · PMID 27155140not yet assessed
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Respiratory system involvement in Costello syndrome ↗American Journal of Medical Genetics Part A · 2016 · PMID 27102959not yet assessed
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Current status and recommendations for biomarkers and biobanking in neurofibromatosis ↗Neurology · 2016 · PMID 27527649not yet assessed
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Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1 ↗American Journal of Medical Genetics Part A · 2016 · PMID 27862945not yet assessed
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The Splicing Efficiency of Activating HRAS Mutations Can Determine Costello Syndrome Phenotype and Frequency in Cancer ↗PLoS Genetics · 2016 · PMID 27195699not yet assessed
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Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia ↗Nature Communications · 2015 · PMID 26387913not yet assessed
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Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure ↗Genetics in Medicine · 2015 · PMID 26248010not yet assessed
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Genetic Variants Associated with Port-Wine Stains ↗PLoS ONE · 2015 · PMID 26192947not yet assessed
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Evaluation of somatic mutations in tibial pseudarthrosis samples in neurofibromatosis type 1 ↗Journal of Medical Genetics · 2015 · PMID 25612910not yet assessed
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An attenuated phenotype of Costello syndrome in three unrelated individuals with a <i>HRAS</i> c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequencesAmerican Journal of Medical Genetics Part A · 2015 · PMID 25914166L1 No computation
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Dystrophic Spinal Deformities in a Neurofibromatosis Type 1 Murine Model ↗PLoS ONE · 2015 · PMID 25786243not yet assessed
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Epidermal Growth Factor (EGFR) copy number aberrations in esophageal and gastro-esophageal junctional carcinoma ↗Molecular Cytogenetics · 2015 · PMID 26478746not yet assessed
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Erratum: Corrigendum: Asfotase-α improves bone growth, mineralization and strength in mouse models of neurofibromatosis type-1 ↗Nature Medicine · 2015 · PMID 25849275not yet assessed
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Dystrophic spinal deformities in a neurofibromatosis type 1 murine modelPMC · 2015not yet assessed
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An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge ↗Genome biology · 2014 · PMID 24667040not yet assessed
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Function and disability in children with Costello syndrome and Cardiofaciocutaneous syndrome ↗American Journal of Medical Genetics Part A · 2014 · PMID 25346259not yet assessed
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Goltz syndrome and <i>PORCN</i> mosaicism ↗International Journal of Dermatology · 2014 · PMID 25040319not yet assessed
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Neural tube defects and atypical deletion on 22q11.2 ↗American Journal of Medical Genetics Part A · 2014 · PMID 25123577not yet assessed
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Epidermal growth factor receptor copy number gain (EGFR CNG) and response to gefitinib in esophageal cancer (EC): Results of a biomarker analysis of a phase III trial of gefitinib versus placebo (TRANS-COG). ↗Journal of Clinical Oncology · 2014not yet assessed
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131: Spontaneous preterm birth risk among inter-racial/ethnic couples ↗American Journal of Obstetrics and Gynecology · 2014not yet assessed
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RAILWAYS ↗Cambridge University Press eBooks · 2014not yet assessed
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STEAM NAVIGATION ↗Cambridge University Press eBooks · 2014not yet assessed
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Approaches to Treating NF1 Tibial Pseudarthrosis ↗Journal of Pediatric Orthopaedics · 2013 · PMID 23482262not yet assessed
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Decreased bone mineral density in Costello syndrome ↗Molecular Genetics and Metabolism · 2013 · PMID 24246682not yet assessed
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The generalized bone phenotype in children with neurofibromatosis 1: A sibling matched case–control study ↗American Journal of Medical Genetics Part A · 2013 · PMID 23713011not yet assessed
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Fractures in Children With Neurofibromatosis Type 1 From Two <scp>NF</scp> Clinics ↗American Journal of Medical Genetics Part A · 2013 · PMID 23529831not yet assessed
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RASA1-Related DisordersUniversity of Washington, Seattle eBooks · 2013not yet assessed
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Neurofibromatosis Type 1 and Dystrophic Scoliosis: A Multicenter Study of Accuracy of Surgeons’ Radiographic Assessment ↗The Spine Journal · 2013not yet assessed
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The Principles and Practice of Canal and River Engineering ↗Cambridge University Press eBooks · 2013not yet assessed
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CROSSING OF NAVIGATIONS BY RAILWAY BRIDGES ↗Cambridge University Press eBooks · 2013not yet assessed
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Neurofibromatosis Type I and Scoliosis: A Multicenter Study to Determine Radiographic Predictors of Dystrophic Scoliosis ↗The Spine Journal · 2013not yet assessed
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TIDAL PROPAGATION AND TIDAL CURRENTS OF RIVERS ↗Cambridge University Press eBooks · 2013not yet assessed
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not yet assessed
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Peripheral muscle weakness in RASopathies ↗Muscle & Nerve · 2012 · PMID 22907230not yet assessed
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Gastrointestinal Bleeding in Infantile Hemangioma: A Complication of Segmental, Rather than Multifocal, Infantile Hemangiomas ↗The Journal of Pediatrics · 2012 · PMID 22240112not yet assessed
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Copy Number Variation Analysis in 98 Individuals with PHACE Syndrome ↗Journal of Investigative Dermatology · 2012 · PMID 23096700not yet assessed
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Candidate locus analysis for PHACE syndrome ↗American Journal of Medical Genetics Part A · 2012 · PMID 22544659not yet assessed
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The genetics of vascular anomalies ↗Current Opinion in Otolaryngology & Head & Neck Surgery · 2012 · PMID 22913934not yet assessed
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Effects of a Plyometric Training Program for 3 Children With Neurofibromatosis Type 1 ↗Pediatric Physical Therapy · 2012 · PMID 22466394not yet assessed
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Spinal arteriovenous fistulas in children with hereditary hemorrhagic telangiectasia ↗Journal of Neurosurgery Pediatrics · 2012 · PMID 22656258not yet assessed
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Acute myeloid leukemia presenting in a mother and daughter pair with the identical acquired karyotypic abnormality consisting of inversion 3q21q26 and monosomy 7: a review of possible mechanisms ↗Cancer Genetics · 2012 · PMID 23064135not yet assessed
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not yet assessed
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The musculoskeletal phenotype of the RASopathies ↗American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2011 · PMID 21495174not yet assessed
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Orthopaedic Conditions in Ras/MAPK Related Disorders ↗Journal of Pediatric Orthopaedics · 2011 · PMID 21654472not yet assessed
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Pediatric 25-hydroxyvitamin D concentrationsin neurofibromatosis type 1 ↗Journal of Pediatric Endocrinology and Metabolism · 2011 · PMID 21648285not yet assessed
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Multiple increased osteoclast functions in individuals with neurofibromatosis type 1 ↗American Journal of Medical Genetics Part A · 2011 · PMID 21465658not yet assessed
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Molecular confirmation of HRAS p.G12S in siblings with Costello syndrome ↗American Journal of Medical Genetics Part A · 2011 · PMID 21834037not yet assessed
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Skeletal abnormalities in neurofibromatosis type 1: Approaches to therapeutic options ↗American Journal of Medical Genetics Part A · 2009 · PMID 19764036not yet assessed
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Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and back ↗American Journal of Medical Genetics Part A · 2009 · PMID 20014119not yet assessed
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Health‐related quality of life measures in genetic disorders: An outcome variable for consideration in clinical trials ↗American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2009 · PMID 19621444not yet assessed
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Pigmentary Findings in Neurofibromatosis Type 1–like Syndrome (Legius Syndrome) ↗JAMA · 2009 · PMID 19920242not yet assessed
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Analysis of Radiographic Characteristics of Anterolateral Bowing of the Leg Before Fracture in Neurofibromatosis Type 1 ↗Journal of Pediatric Orthopaedics · 2009 · PMID 19461382not yet assessed
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Characterisation of chromosomal aberrations involved in acquired docetaxel resistance in human breast cancer cell linesChromosome Research · 2009not yet assessed
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Bone Mineral Density in Children With Neurofibromatosis Type 1 ↗Journal of Pediatric Orthopaedics · 2008 · PMID 18812910not yet assessed
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Neurofibromatosis Type 1 and Other Syndromes of the Ras Pathway ↗Monographs in human genetics · 2008not yet assessed
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The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1 ↗Genetics in Medicine · 2007 · PMID 17666887not yet assessed
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Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the <i>SHOX</i> and <i>SOX3</i> genes ↗American Journal of Medical Genetics Part A · 2007 · PMID 17994562not yet assessed
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A new distal arthrogryposis syndrome characterized by plantar flexion contractures ↗American Journal of Medical Genetics Part A · 2006 · PMID 17103435not yet assessed
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Enabling site development through natural attenuation and plume stabilisation monitoring at a former gas works in Dartford, UK: a corporate approach and the lessons learned ↗Land Contamination & Reclamation · 2006not yet assessed
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Tsunamis and Earthquakes: What Physics Is Interesting? ↗Physics Today · 2005not yet assessed
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Genomic changes identified by comparative genomic hybridisation in docetaxel-resistant breast cancer cell lines ↗European Journal of Cancer · 2005 · PMID 15862759not yet assessed
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Tsunamis and Earthquakes: what Physics is Interesting?CaltechAUTHORS (California Institute of Technology) · 2005not yet assessed
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Identification of minimal regions of genomic alteration associated with docetaxel resistance in breast cancer cells.2005not yet assessed
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Identifying genetic pathways during the evolution of docetaxel resistance in breast cancer cells2005not yet assessed
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Wigner Not the ‘W’ in WKB ↗Physics Today · 2005not yet assessed
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Genetic pathways involved in the evolution of acquired resistance to docetaxel in breast cancer cells.2005not yet assessed
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THE NATURAL HISTORY OF FREEMAN-SHELDON SYNDROME. ↗Journal of Investigative Medicine · 2004not yet assessed
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Genetic pathways in "early" and "late" acquired resistance to docetaxel in breast cancer cells.2004not yet assessed
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Fatal myelodysplastic syndrome developing during therapy with imatinib mesylate and characterised by the emergence of complex Philadelphia negative clones ↗Leukemia · 2003 · PMID 12646955not yet assessed
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Detection of cryptic MLL insertions using a commercial dual-color fluorescence in situ hybridization probe ↗Cancer Genetics and Cytogenetics · 2003 · PMID 14580777not yet assessed
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Detection of a common amplification of 7q in docetaxel resistant breast cancer cell lines by comparative hybridisationEuropean Journal of Cancer · 2003not yet assessed
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Characterisation of docetaxel resistant breast cancer cell lines.2003not yet assessed
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Comparative genomic hybridisation (CGH) identifies genetic events involved in bladder cancer progression.European Journal of Surgical Oncology · 2003not yet assessed
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Comparative genomic hybridisation analyses of genetic changes associated with docetaxel resistance in breast cancer cells.2003not yet assessed
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Synergistic effect of fatty acids on docetaxel-induced apoptosis in prostate cancer cells.2003not yet assessed
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Amplification of HER2 is not involved in resistance to docetaxel in breast cancer cell lines.2003not yet assessed
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Interim analysis of a phase II study of the safety and efficacy of gemtuzumab ozogamicin (Mylotarg (R)) given in combination with cytarabine and daunorubicin to patients < 60 years old with untreated acute myeloid leukemia.Blood · 2002not yet assessed
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Advise or consent? Issues in genetic testing of adolescents. ↗PubMed · 2002 · PMID 11986032not yet assessed
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Hydranencephaly in an infant with vascular malformations ↗American Journal of Medical Genetics · 2001 · PMID 11754063not yet assessed
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Colorectal cancer genomics: evidence for multiple genotypes which influence survival ↗British Journal of Cancer · 2001 · PMID 11720434not yet assessed
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True ↗British Journal of Cancer · 2001not yet assessed
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Characterization of the Topoisomerase I Locus in Human Colorectal Cancer ↗Cancer Genetics and Cytogenetics · 2000 · PMID 10958942not yet assessed
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Comparative genomic hybridization and chromosomal instability in solid tumours ↗British Journal of Cancer · 1999 · PMID 10360667not yet assessed
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Translocation (X;5)(q13;q33) in Essential Thrombocythemia ↗Cancer Genetics and Cytogenetics · 1999 · PMID 10526541not yet assessed
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Comparative genomic hybridization analysis of chromosomal alterations induced by the development of resistance to thymidylate synthase inhibitors. ↗PubMed · 1998 · PMID 9823306not yet assessed
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Acute promyelocytic leukaemia with t(11;17)(q23;q12‐21) and a good initial response to prolonged ATRA and combination chemotherapy ↗British Journal of Haematology · 1998 · PMID 9488621not yet assessed
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Mulvihill-Smith progeria-like syndrome: A further report with delineation of phenotype, immunologic deficits, and novel observation of fibroblast abnormalities ↗American Journal of Medical Genetics · 1997 · PMID 9066884not yet assessed
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Cranial desmoid tumor associated with homozygous inactivation of the adenomatous polyposis coli gene in a 2‐year‐old girl with familial adenomatous polyposis ↗Cancer · 1996 · PMID 8608492not yet assessed
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A prototype system for early geometric configuration design ↗Computers in Industry · 1996not yet assessed
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not yet assessed
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Anion ordering in aged stabilized bismuth oxide ↗Materials Letters · 1995not yet assessed
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Criteria for Performing Multiple Dosimetry ↗Health Physics · 1995 · PMID 7558852not yet assessed
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Aging phenomenon of stabilized bismuth oxides ↗Materials Research Bulletin · 1994not yet assessed
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Structure and corrosion properties of Fe/Zr multilayers ↗Journal of Magnetism and Magnetic Materials · 1993not yet assessed
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Modeling uphill diffusion of Mg implants in GaAs using <scp>suprem</scp>-<scp>i</scp> <scp>v</scp> ↗Journal of Applied Physics · 1992not yet assessed
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Evidence for complete homozygosity of chromosome 17, containing a mutated p53 gene in a case of poorly differentiated ovarian serous adenocarcinoma ↗Cancer Genetics and Cytogenetics · 1992not yet assessed
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Hole-dependent diffusion of implanted Mg in GaAs ↗Applied Physics Letters · 1991not yet assessed
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Spectroscopic investigation of oxygen vacancies in solid oxide electrolytes ↗Applied Physics A · 1990not yet assessed
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Diffusion and hardness studies in mercury zinc telluride ↗Journal of Vacuum Science & Technology A Vacuum Surfaces and Films · 1990not yet assessed
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The relationship between component self-diffusion coefficients and interdiffusion coefficient for pseudobinary systems ↗Journal of Physics and Chemistry of Solids · 1990not yet assessed
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Electrochemical abatement of pollutants NO sub x and SO sub x in a solid-oxide electrolyte reactorOSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) · 1990not yet assessed
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Solid state oxygen kinetics in Er 2 O 3 stabilized Bi 2 O 31990not yet assessed
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The Determination of the Free Energy of Formation of Binary Tellurides Using Lithium Coulometric Titration Techniques ↗Journal of The Electrochemical Society · 1989not yet assessed
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An aetiological study of isochromosome‐X Turner's syndrome ↗Clinical Genetics · 1989 · PMID 2766563not yet assessed
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Diffusion of Ion Implanted Mg and Be in GaAs ↗MRS Proceedings · 1989not yet assessed
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not yet assessed
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The Role of Charged Point Defects on the Diffusion Behavior of Silicon in GaAs ↗MRS Proceedings · 1989not yet assessed
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Hardness and Elastic Modulus Measurements in CdTe and ZnTe Thin Film and Bulk Samples and ZnTe-CdTe Superlattices ↗MRS Proceedings · 1988not yet assessed
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Diffusion studies in the Hg<sub>1−<i>x</i></sub>Cd<sub><i>x</i></sub>Te system ↗Journal of Vacuum Science & Technology A Vacuum Surfaces and Films · 1988not yet assessed
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Interdiffusion in mercury cadmium telluride evaluated from vapor phase growth kinetics ↗physica status solidi (a) · 1988not yet assessed
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Isothermal vapor phase epitaxy of mercury cadmium telluride ↗Journal of Crystal Growth · 1987not yet assessed
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Interdiffusion and related defect mechanisms in the HgTe–CdTe system ↗Journal of Vacuum Science & Technology A Vacuum Surfaces and Films · 1987not yet assessed
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not yet assessed
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Characterization of chemically deoxidized liquid phase epitaxial GaAs ↗Solid-State Electronics · 1987not yet assessed
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ChemInform Abstract: Isothermal Liquid Phase Epitaxial Growth of Mercury Cadmium Telluride. ↗ChemInform · 1987not yet assessed
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Hydrogen permeation in amorphous CuTi and PdSi alloys ↗Journal of Non-Crystalline Solids · 1985not yet assessed
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Oxygen behavior in liquid phase epitaxial GaAs ↗Solid-State Electronics · 1985not yet assessed
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Comparison of the effects of oxygen on cobalt and cobalt-chromium thin films ↗IEEE Transactions on Magnetics · 1985not yet assessed
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Ternary phase equilibria in the Ga-As-Cr system and its relevance to diffusion and solubility studies ↗Journal of Physics and Chemistry of Solids · 1985not yet assessed
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A comparison of the crystallization behavior of liquid-quenched and vapor-quenched amorphous Cu60Ti40 ↗Journal of Non-Crystalline Solids · 1984not yet assessed
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Mammary hypertrophy in an ovariohysterectomized cat. ↗PubMed · 1983 · PMID 17422254not yet assessed
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In situ electrochemical monitoring and control of oxygen in liquid phase epitaxial growth of GaAs ↗Journal of Crystal Growth · 1983not yet assessed
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Crystallization of an amorphous Cu60Ti40 alloy prepared by planar magnetron sputtering ↗Acta Metallurgica · 1983not yet assessed
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Mechanism of graphite baffle gettering in organometallic vapor phase epitaxy; Adsorption of trimethylaluminum on graphite ↗Journal of Electronic Materials · 1983not yet assessed
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not yet assessed
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Influence of Annealing on the Electrical Conductivity of Polycrystalline ZrO <sub>2</sub> +8 Wt% Y <sub>2</sub> O <sub>3</sub> ↗Journal of the American Ceramic Society · 1982not yet assessed
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The influence of solutes on kinetics and thermodynamics of liquid indium-oxygen systems ↗Metallurgical Transactions B · 1982not yet assessed
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Correlations for thermodynamic and kinetic properties of gas solutes in liquid metal solventsOSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) · 1982not yet assessed
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THE VAPOR PHASE INTERACTION OF TRIMETHYLALUMINUM WITH GRAPHITE DURING OMVPE ↗Le Journal de Physique Colloques · 1982not yet assessed
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not yet assessed
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ChemInform Abstract: THE INFLUENCE OF SOLUTE ADDITIONS OF COPPER AND SILVER ON THE DIFFUSIVITY AND THERMODYNAMIC PROPERTIES OF OXYGEN IN LIQUID INDIUM ↗ChemInform · 1982not yet assessed
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ChemInform Abstract: THE INFLUENCE OF SOLUTE ADDITIONS OF TIN, LEAD AND TITANIUM ON THE KINETICS AND THERMODYNAMICS OF THE LIQUID INDIUM‐OXYGEN SYSTEM ↗ChemInform · 1982not yet assessed
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Phase separation in vapor quench synthesized noncrystalline copper zirconium alloys ↗Applied Physics Letters · 1981not yet assessed
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An electrochemical study of the solubility and diffusivity of oxygen in the respective liquid metals indium, gallium, antimony and bismuth ↗Journal of Electroanalytical Chemistry · 1981not yet assessed
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The influence of solute additions of tin, lead and titanium on the kinetics and thermodynamics of the liquid In-O system ↗Journal of the Less Common Metals · 1981not yet assessed
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Experimental problems in the use of solid oxide electrolytes ↗Journal of Applied Electrochemistry · 1981not yet assessed
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The influence of Ti and Zr additions on GaAs liquid phase epitaxial growth ↗Applied Physics Letters · 1980not yet assessed
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Observations on binary clusters formed upon expansion of argon mixtures ↗Chemical Physics · 1980not yet assessed
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Characterization of GaN epitaxial layers using ↗Journal of Electronic Materials · 1977not yet assessed
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Niobium diffusion in pyrolytic graphiteOSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) · 1976not yet assessed
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Synthesis and Properties of ZnGeN[sub 2] ↗Journal of The Electrochemical Society · 1974not yet assessed
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Violet luminescence of Mg-doped GaN ↗Applied Physics Letters · 1973not yet assessed
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Oxygen Diffusion in Liquid Gallium and Indium ↗Journal of The Electrochemical Society · 1973not yet assessed
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The determination of the standard gibbs energies of formation of indium oxides from e.m.f. measurements using a solid oxide electrolyte technique ↗The Journal of Chemical Thermodynamics · 1973not yet assessed
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not yet assessed
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Preparation of Mg-doped GaN diodes exhibiting violet electroluminescence ↗Materials Research Bulletin · 1972not yet assessed
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Determination of the Component Activities in the System In-Ga Using a Solid Oxide Electrolyte Technique ↗Journal of The Electrochemical Society · 1972not yet assessed
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The high temperature electrical properties of ZnTe: Al; self-compensation model in ZnTe ↗Journal of Physics and Chemistry of Solids · 1972not yet assessed
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ChemInform Abstract: BESTIMMUNG DER KOMPONENTENAKTIVITAETEN IM SYST. IN‐GA MITTELS EINES VERFAHRENS MIT EINEM FESTEN OXIDELEKTROLYTEN ↗ChemInform · 1972not yet assessed
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Self-diffusion of Pb and Te in lead telluride ↗Journal of Physics and Chemistry of Solids · 1971not yet assessed
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Self-diffusion of cadmium and tellurium in cadmium telluride ↗Journal of Physics and Chemistry of Solids · 1968not yet assessed
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Core storage as a slave memory for disk storage devices.IFIP Congress · 1968not yet assessed
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Electrical Properties of n‐Type CdSe ↗physica status solidi (b) · 1967not yet assessed
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Solids Under Pressure. William Paul and Douglas M. Warschauer, Eds. McGraw-Hill, New York, 1963. xviii + 478 pp. Illus. $15 ↗Science · 1963not yet assessed
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not yet assessed
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INVESTIGATION OF A TECHNIQUE FOR THE PRODUCTION OF METALLURGICAL STRUCTURES CONTAINING UNIFORMLY DISPERSED STABLE PARTICLES.NASA Technical Reports Server (NASA) · 1961not yet assessed
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PART I. THE SOLUBILITY OF SOME HIGH MELTING POINT METALS IN LIQUID METALS OF LOW FREEZING POINT. PART II. THE SOLUTION RATE OF Cu-Ni ALLOYS IN LEAD. Period covered: October 1, 1957 to December 31, 1958OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) · 1959not yet assessed
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INVESTIGATION OF PHENOMENA RELATED TO LIQUID METAL CORROSION. Period Covered: October 1, 1957 to July 1, 1958OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) · 1958not yet assessed
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A Theory of Liquid Structure ↗The Journal of Chemical Physics · 1937not yet assessed
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The flooded fens: A tidal river and its control ↗Scottish Geographical Magazine · 1937not yet assessed
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CORRESPONDENCE. ON WATERWAYS IN GREAT BRITAIN. ↗Minutes of the Proceedings of the Institution of Civil Engineers · 1906not yet assessed
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Discussion of "Artificial Waterways: Artificial Waterways In the United States"Transactions of the American Society of Civil Engineers · 1905not yet assessed
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Discussion on Artificial Waterways ↗Transactions of the American Society of Civil Engineers · 1905not yet assessed
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CORRESPONDENCE ON CONCRETE-WORK FOR HARBOURS. ↗Minutes of the Proceedings of the Institution of Civil Engineers · 1887not yet assessed
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Description of the Electric Light on the Isle of May ↗Proceedings of the Institution of Mechanical Engineers · 1887not yet assessed
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CORRESPONDENCE. THE ELECTRIC LIGHTHOUSES OF MACQUARIE AND TINO. ↗Minutes of the Proceedings of the Institution of Civil Engineers · 1887not yet assessed
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AILSA CRAIG LIGHTHOUSE AND FOG SIGNALS. (INCLUDES PLATE). ↗Minutes of the Proceedings of the Institution of Civil Engineers · 1887not yet assessed
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CORRESPONDENCE. DREDGING OPERATIONS AND APPLIANCES. ↗Minutes of the Proceedings of the Institution of Civil Engineers · 1887not yet assessed
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The Electric Lighthouse on the Isle of May ↗Scientific American · 1887not yet assessed
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Lighthouse Work ↗Nature · 1887not yet assessed
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Lighthouse Work ↗Nature · 1887not yet assessed
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An Earthquake Invention ↗Nature · 1886not yet assessed
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DESCRIPTION OF A COFFERDAM ADAPTED TO A HARD BOTTOM, USED IN EXCAVATING ROCK FROM THE NAVIGABLE CHANNEL OF THE RIVER RIBBLE; DESIGNED FOR THE RIBBLE NAVIGATION. ↗Transactions of the Institution of Civil Engineers · 1842not yet assessed
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DESCRIPTION OF A COFFRE DAM USED IN EXCAVATING ROCK FROM THE NAVIGABLE CHANNEL OF THE RIVER RIBBLE. ↗Minutes of the Proceedings of the Institution of Civil Engineers · 1841not yet assessed
Full bibliography from OpenAlex; reproducibility verdicts matched by PMID.
Author attribution follows OpenAlex disambiguation, which is imperfect — a researcher's papers can be split across profiles or mixed with a namesake.
Merged across profiles sharing this ORCID where present. See every “Stevenson D” paper on PubMed ↗