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Co-authors
(597)
Yun Li
24
Hulya Kayserili (Hülya Kayserili)
17
Peter Nurnberg (Peter Nürnberg)
17
Gudrun Nurnberg (Gudrun Nürnberg)
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Oya Uyguner
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(41)
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Authors
Bernd Wollnik
Bernd Wollnik,University of Cologne,Genetics & Genealogy,Cardiology,Molecular Biology
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Bernd Wollnik
University of Cologne
Publications:
80
|
Citations:
907
Fields:
Genetics & Genealogy
,
Cardiology
,
Molecular Biology
View FAQ about top research areas and Fields of study
Collaborated with
597 co-authors
from 1993 to 2011
|
Cited by
3982 authors
Cumulative
Annual
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Publications
(80)
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Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta
(
Citations: 6
)
Jutta Becker
,
Oliver Semler
,
Christian Gilissen
,
Yun Li
,
Cecilia Giunta
,
Carsten Bergmann
,
Marianne Rohrbach
,
Friederike Koerber
,
Katharina Zimmermann
,
Brunhilde Wirth
,
Eckhard Schoenau
,
Bernd Wollnik
http://academic.research.microsoft.com/io.ashx?type=5&id=49005389&selfId1=23604498&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 88, no. 3, pp. 362-371, 2011
A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome
(
Citations: 1
)
Guntram Borck
,
Heidrun Wunram
,
Angela Steiert
,
Alexander E. Volk
,
Friederike Körber
,
Sigrid Roters
,
Peter Herkenrath
,
Bernd Wollnik
,
Deborah J. Morris-Rosendahl
,
Christian Kubisch
Journal:
Human Genetics - HUM GENET
, vol. 129, no. 1, pp. 45-50, 2011
Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42
Guntram Borck
,
Atteeq Ur Rehman
,
Kwanghyuk Lee
,
Hans-Martin Pogoda
,
Naseebullah Kakar
,
Simon von Ameln
,
Nicolas Grillet
,
Michael S. Hildebrand
,
Zubair M. Ahmed
,
Gudrun Nürnberg
,
Muhammad Ansar
,
Sulman Basit
Bernd Wollnik
http://academic.research.microsoft.com/io.ashx?type=5&id=49005374&selfId1=23604498&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 88, no. 2, pp. 127-137, 2011
CEP152 is a genome maintenance protein disrupted in Seckel syndrome
E. Kalay
,
G. Yigit
,
Y. Aslan
,
K. E. Brown
,
E. Pohl
,
L. S. Bicknell
,
H. Kayserili
,
Y. Li
,
B. Tuysuz
,
G. Nurnberg
,
W. Kiess
,
M. Koegl
B. Wollnik
http://academic.research.microsoft.com/io.ashx?type=5&id=59744349&selfId1=23604498&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, pp. 23-26, 2011
Craniosynostosis and Multiple Skeletal Anomalies in Humans and Zebrafish Result from a Defect in the Localized Degradation of Retinoic Acid
Kathrin Laue
,
Hans-Martin Pogoda
,
Yasemin Alanay
,
Martin Rachwalski
,
Tim Morgan
,
Christian Kubisch
,
Wilhelm Bloch
,
Bernd Wollnik
,
Matthias Hammerschmidt
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 89, no. 5, pp. 595-606, 2011
Sort by:
Citations
(907 times by 867 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=23604498&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 20, no. 4, pp. 381-388, 2012
In search of triallelism in Bardet-Biedl syndrome
Leen Abu-Safieh
,
Shamsa Al-Anazi
,
Lama Al-Abdi
,
Mais Hashem
,
Hisham Alkuraya
,
Mushari Alamr
,
Mugtaba O Sirelkhatim
,
Zuhair Al-Hassnan
,
Basim Alkuraya
,
Jawahir Y Mohamed
,
Ahmad Al-Salem
,
May Alrashed
http://academic.research.microsoft.com/io.ashx?type=5&id=56548495&selfId1=23604498&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 20, no. 4, pp. 420-427, 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 Cx43-like Connexin Protein Cx40.8 Is Differentially Localized during Fin Ontogeny and Fin Regeneration
Sarah V. Gerhart
,
Diane M. Eble
,
R. Michael Burger
,
Stefan N. Oline
,
Ana Vacaru
,
Kirsten C. Sadler
,
Rebecca Jefferis
,
M. Kathryn Iovine
Journal:
PLOS One
, vol. 7, no. 2, 2012
A Mouse with an N-Ethyl-N-Nitrosourea (ENU) Induced Trp589Arg Galnt3 Mutation Represents a Model for Hyperphosphataemic Familial Tumoural Calcinosis
Christopher T. Esapa
,
Rosie A. Head
,
Jeshmi Jeyabalan
,
Holly Evans
,
Tertius A. Hough
,
Michael T. Cheeseman
,
Eugene G. McNally
,
Andrew J. Carr
,
Gethin P. Thomas
,
Matthew A. Brown
,
Peter I. Croucher
,
Steve D. M. Brown
http://academic.research.microsoft.com/io.ashx?type=5&id=57407369&selfId1=23604498&selfId2=0&maxNumber=12&query=
Journal:
PLOS One
, vol. 7, no. 8, 2012
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