1.
Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs
by Hemani, Gibran
American journal of human genetics, 2013-11-07, Vol.93 (5), p.865-875
2.
Intravascular AAV9 preferentially targets neonatal neurons and adult astrocytes
by Kaspar, Brian K
Nature biotechnology, 2009-01, Vol.27 (1), p.59-65
3.
A Single SNP in an Evolutionary Conserved Region within Intron 86 of the HERC2 Gene Determines Human Blue-Brown Eye Color
by Sturm, Richard A
American journal of human genetics, 2008, Vol.82 (2), p.424-431
4.
Variants in TF and HFE Explain ∼40% of Genetic Variation in Serum-Transferrin Levels
by Benyamin, Beben
American journal of human genetics, 2009-01-09, Vol.84 (1), p.60-65
5.
Human gene for physical performance
by Montgomery, H. E
Nature (London), 1998-05-21, Vol.393 (6682), p.221-222
6.
Global Analysis of DNA Methylation Variation in Adipose Tissue from Twins Reveals Links to Disease-Associated Variants in Distal Regulatory Elements
by Grundberg, Elin
American journal of human genetics, 2013-11-07, Vol.93 (5), p.876-890
7.
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
by Cleynen, Isabelle, PhD
The Lancet (British edition), 2016, Vol.387 (10014), p.156-167
8.
Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage
by Amps, Katherine
Nature biotechnology, 2011, Vol.29 (12), p.1132-1144
9.
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility
by Mbarek, Hamdi
American journal of human genetics, 2016-05-05, Vol.98 (5), p.898-908
10.
Genomewide Linkage Study in 1,176 Affected Sister Pair Families Identifies a Significant Susceptibility Locus for Endometriosis on Chromosome 10q26
by Treloar, Susan A
American journal of human genetics, 2005, Vol.77 (3), p.365-376
11.
Identification of a Systemic Lupus Erythematosus Susceptibility Locus at 11p13 between PDHX and CD44 in a Multiethnic Study
by Lessard, Christopher J
American journal of human genetics, 2011-01-07, Vol.88 (1), p.83-91
12.
Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as Susceptibility Loci for Systemic Lupus Erythematosus in a Large-Scale Multiracial Replication Study
by Lessard, Christopher J
American journal of human genetics, 2012-04-06, Vol.90 (4), p.648-660
13.
Intravesical nadofaragene firadenovec gene therapy for BCG-unresponsive non-muscle-invasive bladder cancer: a single-arm, open-label, repeat-dose clinical trial
by Boorjian, Stephen A
The lancet oncology, 2021-01, Vol.22 (1), p.107-117
14.
Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations
by Shah, Sonia
American journal of human genetics, 2015-07-02, Vol.97 (1), p.75-85
15.
Near-miss SIDS due to Brugada syndrome
by Skinner, J R
Archives of disease in childhood, 2005-05, Vol.90 (5), p.528-529
16.
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype
by Ferreira, Manuel A.R., PhD
Journal of allergy and clinical immunology, 2013, Vol.133 (6), p.1564-1571
17.
Sequence Variants in Three Loci Influence Monocyte Counts and Erythrocyte Volume
by Ferreira, Manuel A.R
American journal of human genetics, 2009-11-13, Vol.85 (5), p.745-749
18.
Genetic Variation Within a Metabolic Motif in the Chromogranin A Promoter: Pleiotropic Influence on Cardiometabolic Risk Traits in Twins
by Rao, Fangwen
American journal of hypertension, 2012-01, Vol.25 (1), p.29-40
19.
PARK3 Influences Age at Onset in Parkinson Disease: A Genome Scan in the GenePD Study
by DeStefano, Anita L
American journal of human genetics, 2002-05, Vol.70 (5), p.1089-1095
20.
Current research priorities in chronic fatigue syndrome/myalgic encephalomyelitis: disease mechanisms, a diagnostic test and specific treatments
by Kerr, J R
Journal of Clinical Pathology, 2007-02, Vol.60 (2), p.113-116
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