Kemal O. Yariz - Concepedia

Author

Kemal O. Yariz

University of Miami

Also Known As

K.O. Yariz, Kemal O Yariz, Kemal O. Yariz, Kemal Yariz, Kemal O. Yariz

Publications

627

Citations

H-Index

Concepts

All Affiliations

University of Miami Dr. John T. Macdonald Foundation Ankara University Loma Linda University Children's National

About

Kemal O. Yariz is an author at University of Miami specializing in genetics, medicine, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	452
2	Endocrinology	2	2	114
3	Arts	1	1	127
4	Molecular Biology	1	1	28
5	Molecular Genetics	1	1	183

Kemal O. Yariz

Publications

604

Citations

H-Index

Page 1

	Year	Citations
Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy Juliane Ramser, Mary Ellen Ahearn, C Lenski, The American Journal of Human Genetics Ube1 Are AssociatedRare DiseasesRare MissenseDevelopmental BiologyMendelian Disorder	2008	183
Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss Kemal O. Yariz, Duygu Duman, Celia Zazo Seco, The American Journal of Human Genetics Developmental BiologyGeneticsAudiologyOtorhinolaryngologyAuditory Physiology	2012	127
Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome Kemal O. Yariz, Tom Walsh, Michail Spiliopoulos, Fertility and Sterility Developmental BiologyMendelian DisorderGenetic DisorderGeneticsReceptor Biology	2011	96
Randomized Phase II Trial of Letrozole plus Anti-MUC1 Antibody AS1402 in Hormone Receptor–Positive Locally Advanced or Metastatic Breast Cancer Nuhad K. Ibrahim, Kemal O. Yariz, Alexey Manikhas, Clinical Cancer Research	2011	69
X-linked infantile spinal muscular atrophy: Clinical definition and molecular mapping Devin Dressman, Mary Ellen Ahearn, Kemal O. Yariz, Genetics in Medicine	2007	32
An Amino Acid Deletion in SZT2 in a Family with Non-Syndromic Intellectual Disability Michelle M. Falcone, Kemal O. Yariz, David Ross, PLoS ONE Mendelian DisorderNon-syndromic Intellectual DisabilityGenetic DisorderExtensive Genetic HeterogeneityGenetics	2013	28
Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations Güney Bademci, Akeem O. Lasisi, Kemal O. Yariz, BMC Medical Genetics	2015	27
Cardiomyopathy with alopecia and palmoplantar keratoderma (CAPK) is caused by a <i>JUP</i> mutation Haydar Ali Erken, Kemal O. Yariz, Duygu Duman, British Journal of Dermatology	2011	24
Effects of heterozygosity for the E180 splice mutation causing growth hormone receptor deficiency in Ecuador on IGF-I, IGFBP-3, and stature Jaime Guevara‐Aguirre, Arlan L. Rosenbloom, Marco Guevara‐Aguirre, Growth Hormone & IGF Research E180 Splice MutationGrowth HormoneHuman GrowthGenetic DisorderGenetics	2007	18

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