Anita S. Kulharya

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.

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)

• WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
  2010 L1 No computation

0 assessed by us (0 reproduced) · 37 not yet assessed — every PubMed paper on record, linked below.

• Mosaic Tetrasomy 13q and Phylloid Hypomelanosis: A Case Report and Review of the Literature ↗

  Pediatric Dermatology · 2014 · PMID 24920397
  not yet assessed
• Complete monosomy 21 confirmed by FISH and array‐CGH ↗

  American Journal of Medical Genetics Part A · 2012 · PMID 22407893
  not yet assessed
• Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: Results from the BABY‐HUG phase III clinical trial ↗

  Pediatric Blood & Cancer · 2011 · PMID 22012708
  not yet assessed
• Genotoxicity Associated with Hydroxyurea Exposure in Infants with Sickle Cell Anemia: Results From the BABY-HUG Phase III Clinical Trial ↗

  Blood · 2011
  not yet assessed
• Acute leukemia with PICALM–MLLT10 fusion gene: diagnostic and treatment struggle ↗

  Cancer Genetics and Cytogenetics · 2010 · PMID 20875875
  not yet assessed
• Near-tetraploidy clone can evolve from a hyperdiploidy clone and cause resistance to lenalidomide and bortezomib in a multiple myeloma patient ↗

  Leukemia Research · 2010 · PMID 20138360
  not yet assessed
• Isolated trisomy 10 in an infant with acute myeloid leukemia: a case report and review of literature. ↗

  PubMed · 2010 · PMID 20830243
  not yet assessed
• A rare case of complete monosomy 21 with multiple osseous, cardiac, and vascular anomalies ↗

  European Journal of Radiology Extra · 2010
  not yet assessed
• Involvement of p54(nrb), a PSF partner protein, in DNA double-strand break repair and radioresistance ↗

  Nucleic Acids Research · 2009 · PMID 19759212
  not yet assessed
• Adrenocortical Cell Lines ↗

  2009
  not yet assessed
• Phenotypic spectrum of 45,X/46,XY males with a ring Y chromosome and bilaterally descended testes ↗

  Fertility and Sterility · 2008 · PMID 18555994
  not yet assessed
• Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features ↗

  American Journal of Medical Genetics Part A · 2008 · PMID 18666229
  not yet assessed
• Long‐term follow‐up and analysis of monozygotic twins concordant for 45,X/46,XY peripheral blood karyotype but discordant for phenotypic sex ↗

  American Journal of Medical Genetics Part A · 2007 · PMID 17935253
  not yet assessed
• Relapsed acute myelogenous leukemia occurring after 18 years with recurrent novel chromosomal abnormality t(18;22)(q23;q11.2) ↗

  Cancer Genetics and Cytogenetics · 2007 · PMID 17854669
  not yet assessed
• Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism ↗

  Fertility and Sterility · 2006 · PMID 16500342
  not yet assessed
• Granular Acute Lymphoblastic Leukemia in Adults: Report of a Case and Review of the Literature ↗

  Southern Medical Journal · 2006 · PMID 16929890
  not yet assessed
• Follicular Lymphoma of the GI Tract - Distinct Entity or Extranodal Manifestation of Nodal Disease?. ↗

  Blood · 2005
  not yet assessed
• Twenty-year follow-up of newborn monozygotic isokaryotypic 45,X/46,XY twins discordant for phenotypic sex ↗

  Fertility and Sterility · 2004
  not yet assessed
• Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients ↗

  The American Journal of Human Genetics · 2003 · PMID 14526392
  not yet assessed
• Radiation therapy depletes extrachromosomally amplified drug resistance genes and oncogenes from tumor cells via micronuclear capture of episomes and double minute chromosomes ↗

  International Journal of Radiation Oncology*Biology*Physics · 2003 · PMID 12605985
  not yet assessed
• Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): Importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies ↗

  American Journal of Medical Genetics · 2002 · PMID 12457409
  not yet assessed
• Cutaneous sclerosing extramedullary hematopoietic tumor in chronic myelogenous leukemia ↗

  Journal of Cutaneous Pathology · 2002 · PMID 12453299
  not yet assessed
• Association between angiotensin II type I receptor polymorphism and resting hemodynamics in black and white youth. ↗

  PubMed · 2002 · PMID 11913624
  not yet assessed
• Maternal complex chromosome rearrangement ascertained through a del (13)(q12.1q14.1) detected in her mildly affected daughter ↗

  American Journal of Medical Genetics · 2001 · PMID 11807870
  not yet assessed
• Exclusion ofSIX6 hemizygosity in a child with anophthalmia, panhypopituitarism and renal failure ↗

  American Journal of Medical Genetics · 2001 · PMID 11746024
  not yet assessed
• Packed red cell transfusion does not compromise chromosome analysis in newborns ↗

  Genetics in Medicine · 2001 · PMID 11478533
  not yet assessed
• Constitutional del(19)(q12q13.1) in a three-year-old girl with severe phenotypic abnormalities affecting multiple organ systems ↗

  American Journal of Medical Genetics · 1998 · PMID 9632168
  not yet assessed
• Kenny-Caffey syndrome and microorchidism ↗

  American Journal of Medical Genetics · 1998 · PMID 9805124
  not yet assessed
• Prenatal diagnosis of a trisomy 17p derived from a <i>de novo</i> non‐mosaic satellited marker ↗

  Clinical Genetics · 1998 · PMID 9842996
  not yet assessed
• Micronuclear entrapment of extrachromosomally amplified genes in irradiated tumor cells ↗

  International Journal of Radiation Oncology*Biology*Physics · 1998
  not yet assessed
• Constitutional del(19)(q12q13.1) in a three‐year‐old girl with severe phenotypic abnormalities affecting multiple organ systems ↗

  American Journal of Medical Genetics · 1998
  not yet assessed
• Prenatal diagnosis of a <i>de novo</i> trisomy 6q22.2→6qter and monosomy lpter→1p36.3. Case report with a 2‐year follow‐up and a brief review of other prenatal cases of partial trisomy 6q ↗

  Clinical Genetics · 1997 · PMID 9111999
  not yet assessed
• Erratum: Prenatal diagnosis of a de novo trisomy 6q22.2→6qter and monosomy 1pter→1p36.3. Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q (Clinical Genetics (1997) 51 (115-117))

  Clinical Genetics · 1997
  not yet assessed
• Interstitial deletions 4q21.1q25 and 4q25q27: Phenotypic variability and relation to Rieger anomaly ↗

  American Journal of Medical Genetics · 1995 · PMID 7717415
  not yet assessed
• Mild phenotypic effects of a de novo deletion Xpter→Xp22.3 and duplication 3pter→3p23 ↗

  American Journal of Medical Genetics · 1995 · PMID 7747779
  not yet assessed
• Three cases of dup(10p)/del(10q) syndrome resulting from maternal pericentric inversion ↗

  American Journal of Medical Genetics · 1993 · PMID 8279477
  not yet assessed
• Trisomy 22: No longer an enigma ↗

  American Journal of Medical Genetics · 1989 · PMID 2624265
  not yet assessed