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Co-authors
(38)
Jonathan L. Haines
2
Stephan L. Zuchner (Stephan L. Züchner)
2
Joseph D. Buxbaum
2
Adam C. Naj
2
Gary W. Beecham
2
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HUM GENET
2
ALZHEIMERS DEMENT
1
AMER J HUM GENET
1
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Academic
Authors
William F. Hulme
William F. Hulme,University of Miami,Genetics & Genealogy,Diseases,Neuroscience
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William F. Hulme
University of Miami
Publications:
4
|
Citations:
23
Fields:
Genetics & Genealogy
,
Diseases
,
Neuroscience
View FAQ about top research areas and Fields of study
Collaborated with
38 co-authors
from 2009 to 2011
|
Cited by
96 authors
Cumulative
Annual
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Publications
(4)
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RefWorks
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Whole-Exome Sequencing Links a Variant in DHDDS to Retinitis Pigmentosa
(
Citations: 2
)
Stephan Züchner
,
Julia Dallman
,
Rong Wen
,
Gary Beecham
,
Adam Naj
,
Amjad Farooq
,
Martin A. Kohli
,
Patrice L. Whitehead
,
William Hulme
,
Ioanna Konidari
,
Yvonne J. K. Edwards
,
Guiqing Cai
http://academic.research.microsoft.com/io.ashx?type=5&id=49005376&selfId1=27622421&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 88, no. 2, pp. 201-206, 2011
Comprehensive Variant Discovery in the Late-Onset Alzheimer’s Disease Susceptibility Gene MTHFD1L Using Next Generation Sequencing Technology
Martin Kohli
,
Adam Naj
,
Jessica Van Baaren
,
William Hulme
,
Gary Beecham
,
Joseph Buxbaum
,
Stephan Zuchner
,
Jonathan Haines
,
John Gilbert
,
Margaret Pericak-Vance
Journal:
Alzheimers & Dementia - ALZHEIMERS DEMENT
, vol. 7, no. 4, pp. S188-S188, 2011
Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West Africans
(
Citations: 12
)
Digna Rosa Velez
,
Christian Wejse
,
Martin E. Stryjewski
,
Eduardo Abbate
,
William F. Hulme
,
Jamie L. Myers
,
Rosa Estevan
,
Sara G. Patillo
,
Rikke Olesen
,
Alessandra Tacconelli
,
Giorgio Sirugo
,
John R. Gilbert
http://academic.research.microsoft.com/io.ashx?type=5&id=34649404&selfId1=27622421&selfId2=0&maxNumber=12&query=
Journal:
Human Genetics - HUM GENET
, vol. 127, no. 1, pp. 65-73, 2010
NOS2A , TLR4 , and IFNGR1 interactions influence pulmonary tuberculosis susceptibility in African-Americans
(
Citations: 9
)
Digna Rosa Velez
,
William F. Hulme
,
Jamie L. Myers
,
J. Brice Weinberg
,
Marc C. Levesque
,
Martin E. Stryjewski
,
Eduardo Abbate
,
Rosa Estevan
,
Sara G. Patillo
,
John R. Gilbert
,
Carol D. Hamilton
,
William K. Scott
Journal:
Human Genetics - HUM GENET
, vol. 126, no. 5, pp. 643-653, 2009
Sort by:
Citations
(23 times by 19 publications)
Variants in the Toll-interacting protein gene are associated with susceptibility to sepsis in the Chinese Han population
(
Citations: 2
)
Zhenju Song
,
Jun Yin
,
Chenling Yao
,
Zhan Sun
,
Mian Shao
,
Yaping Zhang
,
Zhengang Tao
,
Peizhi Huang
,
Chaoyang Tong
Journal:
Critical Care - CRIT CARE
, vol. 15, no. 1, pp. R12-10, 2011
Gene-gene interaction between tuberculosis candidate genes in a South African population
(
Citations: 1
)
Erika de Wit
,
Lize van der Merwe
,
Paul D. van Helden
,
Eileen G. Hoal
Journal:
Mammalian Genome - MAMM GENOME
, vol. 22, no. 1, pp. 100-110, 2011
Comprehensive genetic assessment of a functional TLR9 promoter polymorphism: no replicable association with asthma or asthma-related phenotypes
(
Citations: 2
)
Nancy E Lange
,
Xiaobo Zhou
,
Jessica Lasky-Su
,
Blanca E Himes
,
Ross Lazarus
,
Manuel Soto-Quirós
,
Lydiana Avila
,
Juan C Celedón
,
Catherine M Hawrylowicz
,
Benjamin A Raby
,
Augusto A Litonjua
Journal:
BMC Medical Genetics - BMC MED GENET
, vol. 12, no. 1, pp. 1-9, 2011
Tuberculosis as a complex trait: impact of genetic epidemiological study design
(
Citations: 1
)
Catherine M. SteinAllison
,
Allison R. Baker
Journal:
Mammalian Genome - MAMM GENOME
, vol. 22, no. 1, pp. 91-99, 2011
Exome Sequencing Identifies ZNF644 Mutations in High Myopia
Yi Shi
,
Yingrui Li
,
Dingding Zhang
,
Hao Zhang
,
Yuanfeng Li
,
Fang Lu
,
Xiaoqi Liu
,
Fei He
,
Bo Gong
,
Li Cai
,
Ruiqiang Li
,
Shihuang Liao
http://academic.research.microsoft.com/io.ashx?type=5&id=57409343&selfId1=27622421&selfId2=0&maxNumber=12&query=
Journal:
PLOS Genetics - PLOS GENET
, vol. 7, no. 6, 2011
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