M Bamshad
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Explore the profile of M Bamshad including associated specialties, affiliations and a list of published articles.
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47
Citations
2038
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Recent Articles
1.
Watson N, Buchwald D, Delrow J, Altemeier W, Vitiello M, Pack A, et al.
Sleep
. 2017 Apr;
40(1).
PMID: 28364472
Introduction: Habitual short sleep duration is associated with adverse metabolic, cardiovascular, and inflammatory effects. Co-twin study methodologies account for familial (eg, genetics and shared environmental) confounding, allowing assessment of subtle...
2.
Badiner N, Taylor S, Forlenza K, Lachman R, Bamshad M, Nickerson D, et al.
Clin Genet
. 2016 Dec;
92(2):158-165.
PMID: 27925158
The short-rib polydactyly syndromes (SRPS) are autosomal recessively inherited, genetically heterogeneous skeletal ciliopathies. SRPS phenotypes were historically categorized as types I-IV, with type I first delineated by Saldino and Noonan...
3.
Wallace S, Guo D, Regalado E, Mellor-Crummey L, Bamshad M, Nickerson D, et al.
Clin Genet
. 2016 Jan;
90(4):351-60.
PMID: 26777256
Moyamoya disease (MMD) is a progressive vasculopathy characterized by occlusion of the terminal portion of the internal carotid arteries and its branches, and the formation of compensatory moyamoya collateral vessels....
4.
Regalado E, Guo D, Santos-Cortez R, Hostetler E, Bensend T, Pannu H, et al.
Clin Genet
. 2015 Dec;
89(6):719-23.
PMID: 26621581
Marfan syndrome (MFS) due to mutations in FBN1 is a known cause of thoracic aortic aneurysms and acute aortic dissections (TAAD) associated with pleiotropic manifestations. Genetic predisposition to TAAD can...
5.
Kivisild T, Villems R, Jorde L, Bamshad M, Kumar S, Hedrick P, et al.
Science
. 2007 Sep;
288(5473):1931a.
PMID: 17835098
No abstract available.
6.
Stevenson D, Swoboda K, Sanders R, Bamshad M
Am J Med Genet A
. 2006 Nov;
140(24):2797-801.
PMID: 17103435
The distal arthrogryposis (DA) syndromes are a distinct group of disorders characterized by contractures of two or more different body areas. More than a decade ago, we revised the classification...
7.
Prasad B, Ricker C, Watkins W, Dixon M, Rao B, Naidu J, et al.
Hum Biol
. 2002 Jan;
73(5):715-25.
PMID: 11758691
The aboriginal populations living in the Nicobar Islands are hypothesized to be descendants of people who were part of early human dispersals into Southeast Asia. However, analyses of ethnographic histories,...
8.
Dixon M, Armstrong P, STEVENS D, Bamshad M
Genet Med
. 2001 Sep;
3(5):349-53.
PMID: 11545688
Purpose: To identify the gene causing tarsal/carpal coalition syndrome (TCC). Methods: Individuals from three kindreds with TCC and normal hearing were used to map TCC and screen for mutations in...
9.
van Bokhoven H, Hamel B, Bamshad M, SANGIORGI E, Gurrieri F, Duijf P, et al.
Am J Hum Genet
. 2001 Jul;
69(3):481-92.
PMID: 11462173
p63 mutations have been associated with EEC syndrome (ectrodactyly, ectodermal dysplasia, and cleft lip/palate), as well as with nonsyndromic split hand-split foot malformation (SHFM). We performed p63 mutation analysis in...
10.
Bamshad M, Kivisild T, Watkins W, Dixon M, Ricker C, Rao B, et al.
Genome Res
. 2001 May;
11(6):994-1004.
PMID: 11381027
The origins and affinities of the approximately 1 billion people living on the subcontinent of India have long been contested. This is owing, in part, to the many different waves...