scholarly journals A genome-wide scan in affected sibling pairs with idiopathic recurrent miscarriage suggests genetic linkage

2011 ◽  
Vol 17 (6) ◽  
pp. 379-385 ◽  
Author(s):  
A.M. Kolte ◽  
H.S. Nielsen ◽  
I. Moltke ◽  
B. Degn ◽  
B. Pedersen ◽  
...  
Keyword(s):  
Genetic Linkage ◽  
Recurrent Miscarriage ◽  
Sibling Pairs ◽  
Genome Wide ◽  
A Genome ◽  
Affected Sibling ◽  
Idiopathic Recurrent Miscarriage ◽  
Genome Wide Scan

A Genome-Wide Scan for Linkage to Chromosomal Regions in 382 Sibling Pairs With Schizophrenia or Schizoaffective Disorder

2002 ◽  
Vol 159 (5) ◽  
pp. 803-812 ◽  
Author(s):  
Lynn E. DeLisi ◽  
Sarah H. Shaw ◽  
Timothy J. Crow ◽  
Gail Shields ◽  
Angela B. Smith ◽  
...  
Keyword(s):  
Schizoaffective Disorder ◽  
Sibling Pairs ◽  
Genome Wide ◽  
A Genome ◽  
Genome Wide Scan

scholarly journals A Genome-Wide Scan for Autoimmune Thyroiditis in the Old Order Amish: Replication of Genetic Linkage on Chromosome 5q11.2-q14.3

2003 ◽  
Vol 88 (3) ◽  
pp. 1292-1296 ◽  
Author(s):  
Elsie M. Allen ◽  
Wen-Chi Hsueh ◽  
Mona M. Sabra ◽  
Toni I. Pollin ◽  
Paul W. Ladenson ◽  
...  
Keyword(s):  
Autoimmune Thyroiditis ◽  
Genetic Linkage ◽  
Old Order Amish ◽  
Old Order ◽  
Genome Wide ◽  
A Genome ◽  
Genome Wide Scan

A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia

2006 ◽  
Vol 38 (7) ◽  
pp. 794-800 ◽  
Author(s):  
Anelia Horvath ◽  
Sosipatros Boikos ◽  
Christoforos Giatzakis ◽  
Audrey Robinson-White ◽  
Lionel Groussin ◽  
...  
Keyword(s):  
Gene Encoding ◽  
Genome Wide ◽  
A Genome ◽  
Adrenocortical Hyperplasia ◽  
Genome Wide Scan

scholarly journals A Genome-Wide Scan for Evidence of Selection in a Maize Population Under Long-Term Artificial Selection for Ear Number

Genetics ◽  
2013 ◽  
Vol 196 (3) ◽  
pp. 829-840 ◽  
Author(s):  
Timothy M. Beissinger ◽  
Candice N. Hirsch ◽  
Brieanne Vaillancourt ◽  
Shweta Deshpande ◽  
Kerrie Barry ◽  
...  
Keyword(s):  
Artificial Selection ◽  
Maize Population ◽  
Genome Wide ◽  
A Genome ◽  
Selection For ◽  
Ear Number ◽  
Genome Wide Scan

scholarly journals Assessing linkage of monoamine oxidase B in a genome-wide scan using a univariate variance components approach

1999 ◽  
Vol 17 (S1) ◽  
pp. S49-S54 ◽  
Author(s):  
J.S. Barnholtz ◽  
M. de Andrade ◽  
G.P. Page ◽  
T.M. King ◽  
L.E. Peterson ◽  
...  
Keyword(s):  
Monoamine Oxidase ◽  
Variance Components ◽  
Monoamine Oxidase B ◽  
Genome Wide ◽  
A Genome ◽  
Genome Wide Scan

A genome-wide scan for schizophrenia and psychosis susceptibility loci in families of Mexican and Central American ancestry

2007 ◽  
Vol 144B (2) ◽  
pp. 193-199 ◽  
Author(s):  
M.A. Escamilla ◽  
A. Ontiveros ◽  
H. Nicolini ◽  
H. Raventos ◽  
R. Mendoza ◽  
...  
Keyword(s):  
Central American ◽  
Susceptibility Loci ◽  
Genome Wide ◽  
A Genome ◽  
Genome Wide Scan

scholarly journals A genome-wide scan for a simulated data set using two newly developed methods

1999 ◽  
Vol 17 (S1) ◽  
pp. S621-S626
Author(s):  
Li Hsu ◽  
Corinne Aragaki ◽  
Filemon Quiaoit ◽  
Xiangjing Wang ◽  
Xiubin Xu ◽  
...  
Keyword(s):  
Simulated Data ◽  
Data Set ◽  
Genome Wide ◽  
A Genome ◽  
Genome Wide Scan

Genome-wide linkage scan for exercise stroke volume and cardiac output in the HERITAGE Family Study

2002 ◽  
Vol 10 (2) ◽  
pp. 57-62 ◽  
Author(s):  
Tuomo Rankinen ◽  
Ping An ◽  
Louis Pérusse ◽  
Treva Rice ◽  
Yvon C. Chagnon ◽  
...  
Keyword(s):  
Cardiac Output ◽  
Stroke Volume ◽  
Black Family ◽  
Potential Candidate ◽  
Nuclear Families ◽  
Sibling Pairs ◽  
Suggestive Evidence ◽  
Genome Wide ◽  
A Genome ◽  
Analytical Strategies

A genome-wide linkage scan was performed for genes affecting submaximal exercise cardiac output (Q) and stroke volume (SV) in the sedentary state and their responses to a standardized 20-wk endurance training program. A total of 509 polymorphic markers were used, and 328 pairs of siblings from 99 white nuclear families and 102 sibling pairs from 105 black family units were available. Q and SV were measured in relative steady state during exercise at 50 W (Q50 and SV50, respectively). Baseline phenotypes were adjusted for age, sex, and body surface area (BSA), and the training responses (post-training − baseline, Δ) were adjusted for age, sex, baseline BSA, and baseline value of the phenotype. Three analytical strategies were used: a multipoint variance components linkage analysis using all the family data, and regression-based single- and multipoint linkage analyses using pairs of siblings. In whites, baseline SV50 and ΔSV50 showed promising linkages ( P < 0.0023) with markers on chromosomes 14q31.1 and 10p11.2, respectively. Suggestive evidence of linkage (0.01 > P > 0.0023) for ΔSV50 and Δ Q50 was detected on chromosome 2q31.1 and for baseline SV50 and Q50 on chromosome 9q32-q33. In blacks, markers on 18q11.2 showed promising linkages with baseline Q50. Suggestive evidence of linkage was found in three regions for baseline SV50 (1p21.3, 3q13.3, 12q13.2) and one for baseline SV50 and Q50 (10p14). All these chromosomal regions include several potential candidate genes and therefore warrant further studies in the HERITAGE cohort and other studies.

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