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Co-authors
(165)
Yasemin Alanay
13
Ergul Tuncbilek
7
Koray Boduroglu
7
Dilek Aktas
6
Mehmet Alikasifoglu
4
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(15)
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3
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2
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Authors
Gulen Eda Utine
Gulen Eda Utine,Hacettepe University,Genetics & Genealogy,Anatomy,Ophthalmology
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Gulen Eda Utine
Hacettepe University
Publications:
20
|
Citations:
51
Fields:
Genetics & Genealogy
,
Anatomy
,
Ophthalmology
View FAQ about top research areas and Fields of study
Collaborated with
165 co-authors
from 2005 to 2011
|
Cited by
336 authors
Cumulative
Annual
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Publications
(20)
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RefWorks
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KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes
(
Citations: 1
)
Audrey Putoux
,
Sophie Thomas
,
Karlien L M Coene
,
Erica E Davis
,
Yasemin Alanay
,
Gönül Ogur
,
Elif Uz
,
Daniela Buzas
,
Céline Gomes
,
Sophie Patrier
,
Christopher L Bennett
,
Nadia Elkhartoufi
Gulen Eda Utine
http://academic.research.microsoft.com/io.ashx?type=5&id=56593739&selfId1=23909909&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 43, no. 6, pp. 601-606, 2011
A newborn with overlapping features of AEC and EEC syndromes
T. H. Celik
,
A. Buyukcam
,
P. O. Simsek-Kiper
,
G. E. Utine
,
S. Ersoy-Evans
,
A. Korkmaz
,
H. G. Yntema
,
K. Bodugroglu
,
M. Yurdakok
Journal:
American Journal of Medical Genetics Part A - AM J MED GENET PART A
, pp. 3100-3103, 2011
Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual Disability
G. E. Utine
,
P. Ö. Kiper
,
Y. Alanay
,
E. Tunçbilek
Journal:
Molecular Syndromology
, vol. 2, pp. 64-71, 2011
Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta
(
Citations: 12
)
Yasemin Alanay
,
Hrispima Avaygan
,
Natalia Camacho
,
G. Eda Utine
,
Koray Boduroglu
,
Dilek Aktas
,
Mehmet Alikasifoglu
,
Ergul Tuncbilek
,
Diclehan Orhan
,
Filiz Tiker Bakar
,
Bernard Zabel
,
Andrea Superti-Furga
http://academic.research.microsoft.com/io.ashx?type=5&id=36196388&selfId1=23909909&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 86, no. 4, pp. 551-559, 2010
Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta
Yasemin Alanay
,
Hrispima Avaygan
,
Natalia Camacho
,
G. Eda Utine
,
Koray Boduroglu
,
Dilek Aktas
,
Mehmet Alikasifoglu
,
Ergul Tuncbilek
,
Diclehan Orhan
,
Filiz Tiker Bakar
,
Bernard Zabel
,
Andrea Superti-Furga
http://academic.research.microsoft.com/io.ashx?type=5&id=49005313&selfId1=23909909&selfId2=0&maxNumber=12&query=
Journal:
Journal of Vocational Behavior - J VOCAT BEHAV
, vol. 87, no. 4, pp. 572-573, 2010
Sort by:
Citations
(51 times by 50 publications)
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum
(
Citations: 1
)
Siddharth Banka
,
Ratna Veeramachaneni
,
William Reardon
,
Emma Howard
,
Sancha Bunstone
,
Nicola Ragge
,
Michael J Parker
,
Yanick J Crow
,
Bronwyn Kerr
,
Helen Kingston
,
Kay Metcalfe
,
Kate Chandler
http://academic.research.microsoft.com/io.ashx?type=5&id=56548512&selfId1=23909909&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 20, no. 4, pp. 381-388, 2012
GRHL3/GET1 and Trithorax Group Members Collaborate to Activate the Epidermal Progenitor Differentiation Program
Amelia Soto Hopkin
,
William Gordon
,
Rachel Herndon Klein
,
Francisco Espitia
,
Kenneth Daily
,
Michael Zeller
,
Pierre Baldi
,
Bogi Andersen
Journal:
PLOS Genetics - PLOS GENET
, vol. 8, no. 7, 2012
The Ciliogenic Transcription Factor RFX3 Regulates Early Midline Distribution of Guidepost Neurons Required for Corpus Callosum Development
Carine Benadiba
,
Dario Magnani
,
Mathieu Niquille
,
Laurette Morlé
,
Delphine Valloton
,
Homaira Nawabi
,
Aouatef Ait-Lounis
,
Belkacem Otsmane
,
Walter Reith
,
Thomas Theil
,
Jean-Pierre Hornung
,
Cécile Lebrand
http://academic.research.microsoft.com/io.ashx?type=5&id=57409792&selfId1=23909909&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 8, no. 3, 2012
EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta
Fleur S van Dijk
,
Peter H Byers
,
Raymond Dalgleish
,
Fransiska Malfait
,
Alessandra Maugeri
,
Marianne Rohrbach
,
Sofie Symoens
,
Erik A Sistermans
,
Gerard Pals
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 20, no. 1, pp. 11-19, 2012
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
(
Citations: 1
)
Saima Riazuddin
,
Zubair M Ahmed
,
Rashmi S Hegde
,
Shaheen N Khan
,
Idrees Nasir
,
Uzma Shaukat
,
Sheikh Riazuddin
,
John A Butman
,
Andrew J Griffith
,
Thomas B Friedman
,
Byung Yoon Choi
Journal:
BMC Medical Genetics - BMC MED GENET
, vol. 12, no. 1, pp. 21-11, 2011
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