Sign in
Author
|
Conference
|
Journal
|
Organization
|
Year
|
DOI
Look for results that meet for the following criteria:
since
equal to
before
between
and
Search in all fields of study
Limit my searches in the following fields of study
Agriculture Science
Arts & Humanities
Biology
Chemistry
Computer Science
Economics & Business
Engineering
Environmental Sciences
Geosciences
Material Science
Mathematics
Medicine
Physics
Social Science
Multidisciplinary
Co-authors
(479)
Stephen W. Scherer
30
Anthony J. Brookes
15
Jonathan A. Prince
13
Charlie Wah Heng Lee
11
Jeffrey R. MacDonald
10
Journals
(25)
NAT GENET
6
HUM GENET
4
AMER J HUM GENET
3
GENOME BIOL
3
HUM MOL GENET
3
Keywords
(134)
Embed
Subscribe
Academic
Authors
Lars Feuk
Lars Feuk,Uppsala University,Genetics & Genealogy,Molecular Biology,Neuroscience
Edit
Lars Feuk
Uppsala University
Publications:
51
|
Citations:
5658
Fields:
Genetics & Genealogy
,
Molecular Biology
,
Neuroscience
View FAQ about top research areas and Fields of study
Collaborated with
479 co-authors
from 2000 to 2011
|
Cited by
17799 authors
Cumulative
Annual
Sort by:
Publications
(51)
BibTeX
|
RIS
|
RefWorks
Download
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
(
Citations: 5
)
Dalila Pinto
,
Katayoon Darvishi
,
Xinghua Shi
,
Diana Rajan
,
Diane Rigler
,
Tom Fitzgerald
,
Anath C Lionel
,
Bhooma Thiruvahindrapuram
,
Jeffrey R MacDonald
,
Ryan Mills
,
Aparna Prasad
,
Kristin Noonan
Lars Feuk
http://academic.research.microsoft.com/io.ashx?type=5&id=56648567&selfId1=4155767&selfId2=0&maxNumber=12&query=
Journal:
Nature Biotechnology - NAT BIOTECHNOL
, vol. 29, no. 6, pp. 512-520, 2011
Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain
Adam Ameur
,
Ammar Zaghlool
,
Jonatan Halvardson
,
Anna Wetterbom
,
Ulf Gyllensten
,
Lucia Cavelier
,
Lars Feuk
Journal:
Nature Structural & Molecular Biology - NAT STRUCT MOL BIOL
, vol. 18, no. 12, pp. 1435-1440, 2011
Origins and functional impact of copy number variation in the human genome
(
Citations: 168
)
Donald F. Conrad
,
Dalila Pinto
,
Richard Redon
,
Lars Feuk
,
Omer Gokcumen
,
Yujun Zhang
,
Jan Aerts
,
T. Daniel Andrews
,
Chris Barnes
,
Peter Campbell
,
Tomas Fitzgerald
,
Min Hu
http://academic.research.microsoft.com/io.ashx?type=5&id=45914417&selfId1=4155767&selfId2=0&maxNumber=12&query=
Journal:
Nature
, vol. 464, no. 7289, pp. 704-712, 2010
Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
(
Citations: 60
)
David T. Miller
,
Margaret P. Adam
,
Swaroop Aradhya
,
Leslie G. Biesecker
,
Arthur R. Brothman
,
Nigel P. Carter
,
Deanna M. Church
,
John A. Crolla
,
Evan E. Eichler
,
Charles J. Epstein
,
W. Andrew Faucett
,
Lars Feuk
http://academic.research.microsoft.com/io.ashx?type=5&id=36196402&selfId1=4155767&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 86, no. 5, pp. 749-764, 2010
Towards a comprehensive structural variation map of an individual human genome
(
Citations: 15
)
Andy WC Pang
,
Jeffrey R MacDonald
,
Dalila Pinto
,
John Wei
,
Muhammad A Rafiq
,
Donald F Conrad
,
Matthew E Hurles
,
Charles Lee
,
J Craig Venter
,
Ewen F Kirkness
,
Samuel Levy
,
Lars Feuk
http://academic.research.microsoft.com/io.ashx?type=5&id=38616293&selfId1=4155767&selfId2=0&maxNumber=12&query=
Journal:
Genome Biology - GENOME BIOL
, vol. 11, no. 5, pp. 1-14, 2010
Sort by:
Citations
(5658 times by 3369 publications)
Meta-analysis identifies common variants associated with body mass index in east Asians
(
Citations: 1
)
Wanqing Wen
,
Yoon-Shin Cho
,
Wei Zheng
,
Rajkumar Dorajoo
,
Norihiro Kato
,
Lu Qi
,
Chien-Hsiun Chen
,
Ryan J Delahanty
,
Yukinori Okada
,
Yasuharu Tabara
,
Dongfeng Gu
,
Dingliang Zhu
http://academic.research.microsoft.com/io.ashx?type=5&id=56593592&selfId1=4155767&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 44, no. 3, pp. 307-311, 2012
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
Céline Bellenguez
,
Steve Bevan
,
Andreas Gschwendtner
,
Chris C A Spencer
,
Annette I Burgess
,
Matti Pirinen
,
Caroline A Jackson
,
Matthew Traylor
,
Amy Strange
,
Zhan Su
,
Gavin Band
,
Paul D Syme
http://academic.research.microsoft.com/io.ashx?type=5&id=56593587&selfId1=4155767&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 44, no. 3, pp. 328-333, 2012
Rare structural variation of synapse and neurotransmission genes in autism
(
Citations: 2
)
X Gai
,
H M Xie
,
J C Perin
,
N Takahashi
,
K Murphy
,
A S Wenocur
,
M D'arcy
,
R J O'Hara
,
E Goldmuntz
,
D E Grice
,
T H Shaikh
,
H Hakonarson
http://academic.research.microsoft.com/io.ashx?type=5&id=56564746&selfId1=4155767&selfId2=0&maxNumber=12&query=
Journal:
Molecular Psychiatry - MOL PSYCHIATR
, vol. 17, no. 4, pp. 402-411, 2012
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
Claire S. Leblond
,
Jutta Heinrich
,
Richard Delorme
,
Christian Proepper
,
Catalina Betancur
,
Guillaume Huguet
,
Marina Konyukh
,
Pauline Chaste
,
Elodie Ey
,
Maria Rastam
,
Henrik Anckarsäter
,
Gudrun Nygren
http://academic.research.microsoft.com/io.ashx?type=5&id=57409742&selfId1=4155767&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 8, no. 2, 2012
RNA-Seq Mapping and Detection of Gene Fusions with a Suffix Array Algorithm
Onur Sakarya
,
Heinz Breu
,
Milan Radovich
,
Yongzhi Chen
,
Yulei N. Wang
,
Catalin Barbacioru
,
Sowmi Utiramerur
,
Penn P. Whitley
,
Joel P. Brockman
,
Paolo Vatta
,
Zheng Zhang
,
Liviu Popescu
http://academic.research.microsoft.com/io.ashx?type=5&id=57417701&selfId1=4155767&selfId2=0&maxNumber=12&query=
Journal:
PLOS Computational Biology - PLOS COMPUT BIOL
, vol. 8, no. 4, 2012
Comments