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Co-authors
(495)
Jozef Gecz
33
Michael W. Partington
30
Patrick S. Tarpey
17
Frances Raymond
17
Michael R. Stratton
16
Journals
(39)
J MED GENET
11
AMER J HUM GENET
11
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11
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8
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Authors
Gillian M. Turner
Gillian M. Turner,University of Newcastle,Genetics & Genealogy,Geophysics,Psychiatry & Psychology
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Gillian M. Turner
University of Newcastle
Publications:
102
|
Citations:
1502
Fields:
Genetics & Genealogy
,
Geophysics
,
Psychiatry & Psychology
View FAQ about top research areas and Fields of study
Collaborated with
495 co-authors
from 1989 to 2010
|
Cited by
5646 authors
Cumulative
Annual
Sort by:
Publications
(102)
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RefWorks
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Fine-Scale Survey of X Chromosome Copy Number Variants and Indels Underlying Intellectual Disability
(
Citations: 7
)
Annabel C. Whibley
,
Vincent Plagnol
,
Patrick S. Tarpey
,
Fatima Abidi
,
Tod Fullston
,
Maja K. Choma
,
Catherine A. Boucher
,
Lorraine Shepherd
,
Lionel Willatt
,
Georgina Parkin
,
Raffaella Smith
,
P. Andrew Futreal
Gillian Turner
http://academic.research.microsoft.com/io.ashx?type=5&id=36196484&selfId1=23302904&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 87, no. 2, pp. 173-188, 2010
Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families
(
Citations: 5
)
Kim Hynes
,
Patrick Tarpey
,
Leanne M Dibbens
,
Marta A Bayly
,
Samuel F Berkovic
,
Raffaella Smith
,
Zahyia Al Raisi
,
Samantha J Turner
,
Natasha J Brown
,
Tarishi D Desai
,
Eric Haan
,
Gillian Turner
http://academic.research.microsoft.com/io.ashx?type=5&id=30639317&selfId1=23302904&selfId2=0&maxNumber=12&query=
Journal:
Journal of Medical Genetics - J MED GENET
, vol. 47, no. 3, pp. 211-216, 2010
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation
(
Citations: 2
)
Sinitdhorn Rujirabanjerd
,
John Nelson
,
Patrick S Tarpey
,
Anna Hackett
,
Sarah Edkins
,
F Lucy Raymond
,
Charles E Schwartz
,
Gillian Turner
,
Shigeki Iwase
,
Yang Shi
,
P Andrew Futreal
,
Michael R Stratton
http://academic.research.microsoft.com/io.ashx?type=5&id=37082389&selfId1=23302904&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 18, no. 3, pp. 330-335, 2010
CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes
(
Citations: 5
)
Anna Hackett
,
Patrick S Tarpey
,
Andrea Licata
,
James Cox
,
Annabel Whibley
,
Jackie Boyle
,
Carolyn Rogers
,
John Grigg
,
Michael Partington
,
Roger E Stevenson
,
John Tolmie
,
John RW Yates
Gillian Turner
http://academic.research.microsoft.com/io.ashx?type=5&id=37082424&selfId1=23302904&selfId2=0&maxNumber=12&query=
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 18, no. 5, pp. 544-552, 2010
Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks
(
Citations: 2
)
C. Kerzendorfer
,
A. Whibley
,
G. Carpenter
,
E. Outwin
,
S.-C. Chiang
,
G. Turner
,
C. Schwartz
,
S. El-Khamisy
,
F. L. Raymond
,
M. O'Driscoll
Journal:
Human Molecular Genetics - HUM MOL GENET
, vol. 19, no. 7, pp. 1324-1334, 2010
Sort by:
Citations
(1502 times by 1156 publications)
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
G Kirov
,
A J Pocklington
,
P Holmans
,
D Ivanov
,
M Ikeda
,
D Ruderfer
,
J Moran
,
K Chambert
,
D Toncheva
,
L Georgieva
,
D Grozeva
,
M Fjodorova
http://academic.research.microsoft.com/io.ashx?type=5&id=56564762&selfId1=23302904&selfId2=0&maxNumber=12&query=
Journal:
Molecular Psychiatry - MOL PSYCHIATR
, vol. 17, no. 2, pp. 142-153, 2012
Lack of Wdr13 Gene in Mice Leads to Enhanced Pancreatic Beta Cell Proliferation, Hyperinsulinemia and Mild Obesity
Vijay Pratap Singh
,
B. Jyothi Lakshmi
,
Shalu Singh
,
Vanya Shah
,
Sandeep Goel
,
D. Partha Sarathi
,
Satish Kumar
Journal:
PLOS One
, vol. 7, no. 6, 2012
Ubiquitin E3 ligases controlling p53 stability
Seong Won Lee
,
Min Woo Seong
,
Young Joo Jeon
,
Chin Ha Chung
Journal:
Animal Cells and Systems - ANIM CELLS SYST
, vol. ahead-of-p, no. ahead-of-p, pp. 1-10, 2012
Algorithmic Approach for Methyl-CpG Binding Protein 2 (MECP2) Gene Testing in Patients With Neurodevelopmental Disabilities
Jennifer N. Sanmann
,
G. Bradley Schaefer
,
Bruce A. Buehler
,
Warren G. Sanger
Journal:
Journal of Child Neurology - JCN
, vol. 27, no. 3, pp. 346-354, 2012
Regulation of cytoplasmic mRNA decay
Daniel R. Schoenberg
,
Lynne E. Maquat
Journal:
Nature Reviews Genetics - NAT REV GENET
, vol. 13, no. 4, pp. 246-259, 2012
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