Author

Kemal O. Yariz

Observed names: K.O. Yariz, Kemal O Yariz, Kemal Yariz, Kemal O. Yariz

Institution: University of Miami

Observed institutions: The University of Texas MD Anderson Cancer Center, University of Miami, Institute of Oncology NN Petrov, City Clinical Oncology Center, Dr. John T. Macdonald Foundation, Dnipro State Medical University

OpenAlex ID: A5111439197

Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy

2008 · Juliane Ramser, Mary Ellen Ahearn, et al. · The American Journal of Human Genetics · 186

Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

2012 · Kemal O. Yariz, Duygu Duman, et al. · The American Journal of Human Genetics · 131

Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome

2011 · Kemal O. Yariz, Tom Walsh, et al. · Fertility and Sterility · 88

Randomized Phase II Trial of Letrozole plus Anti-MUC1 Antibody AS1402 in Hormone Receptor–Positive Locally Advanced or Metastatic Breast Cancer

2011 · Nuhad K. Ibrahim, Kemal O. Yariz, et al. · Clinical Cancer Research · 71

X-linked infantile spinal muscular atrophy: Clinical definition and molecular mapping

2007 · Devin Dressman, Mary Ellen Ahearn, et al. · Genetics in Medicine · 32

An Amino Acid Deletion in SZT2 in a Family with Non-Syndromic Intellectual Disability

2013 · Michelle Falcone, Kemal O. Yariz, et al. · PLoS ONE · 28

Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations

2015 · Guney Bademci, Akeem O Lasisi, et al. · BMC Medical Genetics · 23

A homozygous SIX6 mutation is associated with optic disc anomalies and macular atrophy and reduces retinal ganglion cell differentiation

2014 · K.O. Yariz, Y.B. Sakalar, et al. · Clinical Genetics · 23

Cardiomyopathy with alopecia and palmoplantar keratoderma (CAPK) is caused by a JUP mutation

2011 · H. Erken, K.O. Yariz, et al. · British Journal of Dermatology · 23

Effects of heterozygosity for the E180 splice mutation causing growth hormone receptor deficiency in Ecuador on IGF-I, IGFBP-3, and stature

2007 · Jaime Guevara-Aguirre, Arlan L. Rosenbloom, et al. · Growth Hormone & IGF Research · 19

X-linked lethal infantile (XL)-SMA: new clinical information, variant phenotypes, and candidate disease gene studies.

2004 · Mary Ellen Ahearn, Devin Dressman, et al. · mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich) · 1

Abstract 4196: Identification and investigation of ethnic specific gene expression differences in non-cancerous breast tissue

2012 · Lisa L. Baumbach-Reardon, Carmen Gomez, et al. · Cancer Research

The Chronicles of X-Linked Spinal Muscular Atrophy: The Linkage, The Gene and The SMN Complex

2008 · Kemal O. Yariz

Works count: 14

Citation count: 625

H-index: 10

I10-index: 10