Anita S. Kulharya

Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

Regina Ensenauer, Adewale Adeyinka, Heather C. Flynn et al. · The American Journal of Human Genetics · 2003 · 376 citations · Full text

Cytogenetics, Genetic Disorder, Genetics +8

WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Hyung‐Goo Kim, Jang-Won Ahn, Ingo Kurth et al. · The American Journal of Human Genetics · 2010 · 192 citations · Full text

Is Mutated, Transcriptional Regulation, Developmental Biology +9

Phenotypic spectrum of 45,X/46,XY males with a ring Y chromosome and bilaterally descended testes

Lawrence C. Layman, Sandra P.T. Tho, Andrew Clark et al. · Fertility and Sterility · 2008 · 121 citations · Full text

Cytogenetics, Medicine, Genetics +12

Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism

Balasubramanian Bhagavath, Robert H. Podolsky, Metin Özata et al. · Fertility and Sterility · 2006 · 111 citations

Infertility, Urology, Andrology +14

Long‐term follow‐up and analysis of monozygotic twins concordant for 45,X/46,XY peripheral blood karyotype but discordant for phenotypic sex

Sandra P.T. Tho, Robert W. Jackson, Anita S. Kulharya et al. · American Journal of Medical Genetics Part A · 2007 · 91 citations