Selectivity in Genetic Association with Sub-classified Migraine in Women

Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy

(2013) Anne-Karin Arndt et al.   AMERICAN JOURNAL OF HUMAN GENETICS

TRP Channels and Pain

(2013) David Julius   Annual Review of Cell and Developmental Biology

Distinctive anatomical and physiological features of migraine aura revealed by 18 years of recording

(2013) Jakob Møller Hansen et al.   BRAIN

The International Classification of Headache Disorders, 3rd edition (beta version)

(2013)   CEPHALALGIA

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

(2013)   LANCET

Mental health: On the spectrum

(2013) David Adam   NATURE

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

(2013) S Hong Lee et al.   NATURE GENETICS

Discovery and refinement of loci associated with lipid levels

(2013) Cristen J Willer et al.   NATURE GENETICS

Why has it taken so long for biological psychiatry to develop clinical tests and what to do about it?

(2012) S Kapur et al.   MOLECULAR PSYCHIATRY

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

(2012) Kerstin U Ludwig et al.   NATURE GENETICS

Genome-wide association analysis identifies susceptibility loci for migraine without aura

(2012) Tobias Freilinger et al.   NATURE GENETICS

A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility

(2012) Hannah C. Cox et al.   NEUROGENETICS

An X Chromosome Association Scan of the Norfolk Island Genetic Isolate Provides Evidence for a Novel Migraine Susceptibility Locus at Xq12

(2012) Bridget H. Maher et al.   PLoS One

Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1

(2011) Matthew J. Bown et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Migraine features, associated symptoms and triggers: A principal component analysis in the Women’s Health Study

(2011) Markus Schürks et al.   CEPHALALGIA

Modifiers and Subtype-Specific Analyses in Whole-Genome Association Studies: A Likelihood Framework

(2011) Phil H. Lee et al.   HUMAN HEREDITY

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function

(2011) María Soler Artigas et al.   NATURE GENETICS

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

(2011) Daniel I Chasman et al.   NATURE GENETICS

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

(2010) Yun Li et al.   GENETIC EPIDEMIOLOGY

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

(2010) Verneri Anttila et al.   NATURE GENETICS

Agreement of Self-Reported Migraine With ICHD-II Criteria in the Women's Health Study

(2009) M Schürks et al.   CEPHALALGIA

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

(2009) L. A. Hindorff et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

PRDM16 controls a brown fat/skeletal muscle switch

(2008) Patrick Seale et al.   NATURE

Rationale, Design, and Methodology of the Women's Genome Health Study: A Genome-Wide Association Study of More Than 25 000 Initially Healthy American Women

(2007) P. M Ridker et al.   CLINICAL CHEMISTRY