Concepedia

Ahmet Karagüzel

AK

Statistics

Publications

20

Citations

1.1K

H-Index

15

Active since

1991

Affiliations

Karadeniz Technical University(Current)

Radboud University Nijmegen

Radboud University Medical Center

University of Cologne

Istanbul University

Ahmet Karagüzel is an author at Karadeniz Technical University specializing in life sciences, genetics, and molecular genetics.

Publications per year

1991–2012

20

Publications

20

CEP152 is a genome maintenance protein disrupted in Seckel syndrome

Ersan Kalay, Gökhan Yigit, Yakup Aslan et al. · Nature Genetics · 2010 · 226 citations · Full text

, , +3

Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35

Rob W.J. Collin, Ersan Kalay, Muhammad Tariq et al. · The American Journal of Human Genetics · 2008 · 129 citations · Full text

, , +8

Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

Zubair M. Ahmed, Saber Masmoudi, Ersan Kalay et al. · Nature Genetics · 2008 · 87 citations · Full text

, , +15

The frequency of chromosomal abnormalities in patients with reproductive failure

Figen Celep, Ahmet Karagüzel, Mehmet Özeren et al. · European Journal of Obstetrics & Gynecology and Reproductive Biology · 2006 · 74 citations

, , +14

Mutations in the<i>lipoma HMGIC fusion partner-like 5 (LHFPL5)</i>gene cause autosomal recessive nonsyndromic hearing loss

Ersan Kalay, Yun Li, Abdullah Üzümcü et al. · Human Mutation · 2006 · 71 citations

, , +16

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