Detalles de la búsqueda
1.
ComPaSS-GWAS: A method to reduce type I error in genome-wide association studies when replication data are not available.
Genet Epidemiol;
43(1): 102-111, 2019 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-30334581
2.
Genetic associations with childhood brain growth, defined in two longitudinal cohorts.
Genet Epidemiol;
42(4): 405-414, 2018 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-29682794
3.
A common haplotype containing functional CACNA1H variants is frequently coinherited with increased TPSAB1 copy number.
Genet Med;
20(5): 503-512, 2018 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-28933792
4.
Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis.
PLoS Genet;
10(10): e1004575, 2014 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-25329635
5.
Visual Defects in Patients With Pituitary Adenomas: The Myth of Bitemporal Hemianopsia.
AJR Am J Roentgenol;
205(5): W512-8, 2015 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-26496573
6.
Strong Genetic Overlaps Between Dimensional and Categorical Models of Bipolar Disorders in a Family Sample.
medRxiv;
2024 Mar 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-37425936
7.
Intra-familial tests of association between familial idiopathic scoliosis and linked regions on 9q31.3-q34.3 and 16p12.3-q22.2.
Hum Hered;
74(1): 36-44, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-23154503
8.
Exome-wide association study of treatment-resistant depression suggests novel treatment targets.
Sci Rep;
13(1): 12467, 2023 08 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37528149
9.
A resource of induced pluripotent stem cell (iPSC) lines including clinical, genomic, and cellular data from genetically isolated families with mood and psychotic disorders.
Transl Psychiatry;
13(1): 397, 2023 Dec 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-38104115
10.
Necessary and sufficient conditions for equality of sibling and parent-offspring risk of a disease endophenotype in case families.
Ann Hum Genet;
76(1): 86-91, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22091704
11.
The Genetic Basis of Thought Disorder and Language and Communication Disturbances in Schizophrenia.
J Neurolinguistics;
23(3): 176, 2010 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-20161689
12.
Genome-wide association study of café-au-lait macule number in neurofibromatosis type 1.
Mol Genet Genomic Med;
8(10): e1400, 2020 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-32869517
13.
The power of linkage analysis of a disease-related endophenotype using asymmetrically ascertained sib pairs.
Comput Stat Data Anal;
53(5): 1829-1842, 2009 03 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-20160849
14.
Craniopharyngiomas : Radiological Differentiation of Two Types.
J Korean Neurosurg Soc;
59(5): 466-70, 2016 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-27651864
15.
Type I error rates of rare single nucleotide variants are inflated in tests of association with non-normally distributed traits using simple linear regression methods.
BMC Proc;
10(Suppl 7): 385-388, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27980666
16.
A gene-model-free method for linkage analysis of a disease-related-trait based on analysis of proband/sibling pairs.
BMC Genet;
6 Suppl 1: S47, 2005 Dec 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-16451658
17.
Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data.
BMC Proc;
5 Suppl 9: S83, 2011 Nov 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-22373393
18.
Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression.
BMC Proc;
5 Suppl 9: S15, 2011 Nov 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-22373501
19.
Performance of random forests and logic regression methods using mini-exome sequence data.
BMC Proc;
5 Suppl 9: S104, 2011 Nov 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-22373484
20.
A combined genome-wide linkage and association approach to find susceptibility loci for platelet function phenotypes in European American and African American families with coronary artery disease.
BMC Med Genomics;
3: 22, 2010 Jun 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-20529293