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
(1460)
Gerard D. Schellenberg
52
Ellen J. Steinbart
38
James B. Leverenz
31
David Nochlin
30
Hillary P. Lipe
27
Journals
(75)
ANN NEUROL
37
ARCH NEUROL
21
AMER J HUM GENET
15
ALZHEIMERS DEMENT
14
NAT GENET
10
Keywords
(321)
Embed
Subscribe
Academic
Authors
Thomas D. Bird
Thomas D. Bird,University of Washington,Neuroscience,Genetics & Genealogy,Diseases
Edit
Thomas D. Bird
University of Washington
Publications:
271
|
Citations:
9226
Fields:
Neuroscience
,
Genetics & Genealogy
,
Diseases
View FAQ about top research areas and Fields of study
Collaborated with
1460 co-authors
from 1985 to 2011
|
Cited by
22345 authors
Cumulative
Annual
Sort by:
Publications
(271)
BibTeX
|
RIS
|
RefWorks
Download
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
(
Citations: 2
)
Adam C Naj
,
Gyungah Jun
,
Gary W Beecham
,
Li-San Wang
,
Badri Narayan Vardarajan
,
Jacqueline Buros
,
Paul J Gallins
,
Joseph D Buxbaum
,
Gail P Jarvik
,
Paul K Crane
,
Eric B Larson
,
Thomas D Bird
http://academic.research.microsoft.com/io.ashx?type=5&id=56593715&selfId1=10891620&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 43, no. 5, pp. 436-441, 2011
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
(
Citations: 2
)
Günter U Höglinger
,
Nadine M Melhem
,
Dennis W Dickson
,
Patrick M A Sleiman
,
Li-San Wang
,
Lambertus Klei
,
Rosa Rademakers
,
Rohan de Silva
,
Irene Litvan
,
David E Riley
,
John C van Swieten
,
Peter Heutink
Thomas D Bird
http://academic.research.microsoft.com/io.ashx?type=5&id=56593764&selfId1=10891620&selfId2=0&maxNumber=12&query=
Journal:
Nature Genetics - NAT GENET
, vol. 43, no. 7, pp. 699-705, 2011
Mutations in Prickle Orthologs Cause Seizures in Flies, Mice, and Humans
(
Citations: 2
)
Hirotaka Tao
,
J. Robert Manak
,
Levi Sowers
,
Xue Mei
,
Hiroshi Kiyonari
,
Takaya Abe
,
Nader S. Dahdaleh
,
Tian Yang
,
Shu Wu
,
Shan Chen
,
Mark H. Fox
,
Christina Gurnett
Thomas Bird
http://academic.research.microsoft.com/io.ashx?type=5&id=49005375&selfId1=10891620&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 88, no. 2, pp. 138-149, 2011
Biochemical, neuropathological, and neuroimaging characteristics of early-onset Alzheimer's disease due to a novel PSEN1 mutation
John M. Ringman
,
Karen H. Gylys
,
Luis D. Medina
,
Michelle Fox
,
Vladimir Kepe
,
Deborah L. Flores
,
Liana G. Apostolova
,
Jorge R. Barrio
,
Gary Small
,
Daniel H. Silverman
,
Erin Siu
,
Stephen Cederbaum
Thomas D. Bird
http://academic.research.microsoft.com/io.ashx?type=5&id=49325400&selfId1=10891620&selfId2=0&maxNumber=12&query=
Journal:
Neuroscience Letters - NEUROSCI LETT
, vol. 487, no. 3, pp. 287-292, 2011
Corrigendum to “Biochemical, neuropathological, and neuroimaging characteristics of early-onset Alzheimer's disease due to a novel PSEN1 mutation”
John M. Ringman
,
Karen H. Gylys
,
Luis D. Medina
,
Michelle Fox
,
Vladimir Kepe
,
Deborah L. Flores
,
Liana G. Apostolova
,
Jorge R. Barrio
,
Gary Small
,
Daniel H. Silverman
,
Erin Siu
,
Stephen Cederbaum
Thomas D. Bird
http://academic.research.microsoft.com/io.ashx?type=5&id=49325603&selfId1=10891620&selfId2=0&maxNumber=12&query=
Journal:
Neuroscience Letters - NEUROSCI LETT
, vol. 491, no. 2, pp. 163-163, 2011
Sort by:
Citations
(9226 times by 6965 publications)
Probing sporadic and familial Alzheimer’s disease using induced pluripotent stem cells
Mason A. Israel
,
Shauna H. Yuan
,
Cedric Bardy
,
Sol M. Reyna
,
Yangling Mu
,
Cheryl Herrera
,
Michael P. Hefferan
,
Sebastiaan Van Gorp
,
Kristopher L. Nazor
,
Francesca S. Boscolo
,
Christian T. Carson
,
Louise C. Laurent
http://academic.research.microsoft.com/io.ashx?type=5&id=56632117&selfId1=10891620&selfId2=0&maxNumber=12&query=
Journal:
Nature
, vol. 482, no. 7384, pp. 216-220, 2012
Brain Expression Genome-Wide Association Study (eGWAS) Identifies Human Disease-Associated Variants
Fanggeng Zou
,
High Seng Chai
,
Curtis S. Younkin
,
Mariet Allen
,
Julia Crook
,
V. Shane Pankratz
,
Minerva M. Carrasquillo
,
Christopher N. Rowley
,
Asha A. Nair
,
Sumit Middha
,
Sooraj Maharjan
,
Thuy Nguyen
http://academic.research.microsoft.com/io.ashx?type=5&id=57409926&selfId1=10891620&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 8, no. 6, 2012
Multiple Intravenous Administrations of Human Umbilical Cord Blood Cells Benefit in a Mouse Model of ALS
Svitlana Garbuzova-Davis
,
Maria C. O. Rodrigues
,
Santhia Mirtyl
,
Shanna Turner
,
Shazia Mitha
,
Jasmine Sodhi
,
Subatha Suthakaran
,
David J. Eve
,
Cyndy D. Sanberg
,
Nicole Kuzmin-Nichols
,
Paul R. Sanberg
Journal:
PLOS One
, vol. 7, no. 2, 2012
Genome Wide Association Identifies PPFIA1 as a Candidate Gene for Acute Lung Injury Risk Following Major Trauma
Jason D. Christie
,
Mark M. Wurfel
,
Rui Feng
,
Grant E. OKeefe
,
Jonathan Bradfield
,
Lorraine B. Ware
,
David C. Christiani
,
Carolyn S. Calfee
,
Mitchell J. Cohen
,
Michael Matthay
,
Nuala J. Meyer
,
Cecilia Kim
http://academic.research.microsoft.com/io.ashx?type=5&id=57402088&selfId1=10891620&selfId2=0&maxNumber=12&query=
Journal:
PLOS One
, vol. 7, no. 1, 2012
Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families
Carlos Cruchaga
,
Sumitra Chakraverty
,
Kevin Mayo
,
Francesco L. M. Vallania
,
Robi D. Mitra
,
Kelley Faber
,
Jennifer Williamson
,
Tom Bird
,
Ramon Diaz-Arrastia
,
Tatiana M. Foroud
,
Bradley F. Boeve
,
Neill R. Graff-Radford
http://academic.research.microsoft.com/io.ashx?type=5&id=57402373&selfId1=10891620&selfId2=0&maxNumber=12&query=
Journal:
PLOS One
, vol. 7, no. 2, 2012
Comments