Publications by authors named "Kemal O Yariz"

7Publications

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

Authors:
Guney Bademci Akeem Lasisi Kemal O Yariz Paola Montenegro Ibis Menendez Rodrigo Vinueza Rosario Paredes Germania Moreta Asli Subasioglu Susan Blanton Suat Fitoz Armagan Incesulu Levent Sennaroglu Mustafa Tekin

BMC Med Genet 2015 Feb 25;16. Epub 2015 Feb 25.

John P. Hussmann Institute for Human Genomics and John T. Macdonald Foundation, Department of Human Genetics, Miller school of Medicine, University of Miami, 1501 NW 10th Avenue, BRB-610 (M-860), Miami, FL, 33136, USA.

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February 2015

An amino acid deletion inSZT2 in a family with non-syndromic intellectual disability.

Authors:
Michelle Falcone Kemal O Yariz David B Ross Joseph Foster Ibis Menendez Mustafa Tekin

PLoS One 2013 6;8(12):e82810. Epub 2013 Dec 6.

Dr. John T. Macdonald Department of Human Genetics and John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida, United States of America.

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July 2014

Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.

Authors:
Kemal O Yariz Duygu Duman Celia Zazo Seco Julia Dallman Mingqian Huang Theo A Peters Asli Sirmaci Na Lu Margit Schraders Isaac Skromne Jaap Oostrik Oscar Diaz-Horta Juan I Young Suna Tokgoz-Yilmaz Ozlem Konukseven Hashem Shahin Lisette Hetterschijt Moien Kanaan Anne M M Oonk Yvonne J K Edwards Huawei Li Semra Atalay Susan Blanton Alexandra A Desmidt Xue-Zhong Liu Ronald J E Pennings Zhongmin Lu Zheng-Yi Chen Hannie Kremer Mustafa Tekin

Am J Hum Genet 2012 11;91(5):872-82

John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL 33136, USA.

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November 2012

Randomized phase II trial of letrozole plus anti-MUC1 antibody AS1402 in hormone receptor-positive locally advanced or metastatic breast cancer.

Authors:
Nuhad K Ibrahim Kemal O Yariz Ihor Bondarenko Alexei Manikhas Vladimir Semiglazov Anna Alyasova Volodymyr Komisarenko Yaroslav Shparyk James Lee Murray David Jones Shai Senderovich Albert Chau Fredrik Erlandsson Gary Acton Mark Pegram

Clin Cancer Res 2011 Nov 30;17(21):6822-30. Epub 2011 Aug 30.

Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.

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November 2011

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

Authors:
Kemal O Yariz Tom Walsh Asli Uzak Michail Spiliopoulos Duygu Duman Gogsen Onalan Mary-Claire King Mustafa Tekin

Fertil Steril 2011 Aug 17;96(2):e125-30. Epub 2011 Jun 17.

Department of Human Genetics and Institute for Human Genomics, University of Miami School of Medicine, Miami, Florida, USA.

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August 2011

Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy.

Authors:
Juliane Ramser Mary Ellen Ahearn Claus Lenski Kemal O Yariz Heide Hellebrand Michael von Rhein Robin D Clark Rita K Schmutzler Peter Lichtner Eric P Hoffman Alfons Meindl Lisa Baumbach-Reardon

Am J Hum Genet 2008 Jan;82(1):188-93

Department of Obstetrics and Gynecology, Technical University Munich, 81675 Munich, Germany.

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January 2008

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

Authors:
Devin Dressman Mary Ellen Ahearn Kemal O Yariz Hugo Basterrecha Francisco Martínez Francesc Palau M Michael Barmada Robin Dawn Clark Alfons Meindl Brunhilde Wirth Eric P Hoffman Lisa Baumbach-Reardon

Genet Med 2007 Jan;9(1):52-60

Research Center for Genetic Medicine, Children's National Medical Center, Washington, DC, USA.

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January 2007