User profiles for "author:P Sullivan"

Patrick F Sullivan

Professor of Genetics, University of North Carolina; Professor, MEB, Karolinska Institutet
Verified email at med.unc.edu
Cited by 150871

Genetic epidemiology of major depression: review and meta-analysis

PF Sullivan, MC Neale… - American journal of …, 2000 - Am Psychiatric Assoc
OBJECTIVE: The authors conducted a meta-analysis of relevant data from primary studies of
the genetic epidemiology of major depression. METHOD: The authors searched MEDLINE …

Genetic architectures of psychiatric disorders: the emerging picture and its implications

PF Sullivan, MJ Daly, M O'donovan - Nature Reviews Genetics, 2012 - nature.com
Psychiatric disorders are among the most intractable enigmas in medicine. In the past 5
years, there has been unprecedented progress on the genetics of many of these conditions …

Electric field poled organic electro-optic materials: state of the art and future prospects

LR Dalton, PA Sullivan, DH Bale - Chemical reviews, 2010 - ACS Publications
Information is created, processed, transported, and detected using electrons, photons,
phonons, or plasmons. Of these basic components of information technology, utilization of …

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

…, CM Hultman, P Lichtenstein, EF Thelander, P Sullivan… - Nature, 2009 - nature.com
Schizophrenia is a severe mental disorder with a lifetime risk of about 1%, characterized by
hallucinations, delusions and cognitive deficits, with heritability estimated at up to 80%,. We …

Biological insights from 108 schizophrenia-associated genetic loci

C Pantelis, GN Papadimitriou, S Papiol… - Nature, 2014 - nature.com
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of
alleles, including common alleles of small effect that might be detected by genome-wide …

[HTML][HTML] Analysis of protein-coding genetic variation in 60,706 humans

M Lek, KJ Karczewski, EV Minikel, KE Samocha… - Nature, 2016 - nature.com
Large-scale reference data sets of human genetic variation are critical for the medical and
functional interpretation of DNA sequence changes. Here we describe the aggregation and …

Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

…, CDA Stehouwer, M Stumvoll, P Sullivan… - Nature …, 2021 - nature.com
Trait-associated genetic variants affect complex phenotypes primarily via regulatory
mechanisms on the transcriptome. To investigate the genetics of gene expression, we …

[HTML][HTML] Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence

G Genovese, AK Kähler, RE Handsaker… - … England Journal of …, 2014 - Mass Medical Soc
Background Cancers arise from multiple acquired mutations, which presumably occur over
many years. Early stages in cancer development might be present years before cancers …

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

D Demontis, RK Walters, J Martin, M Mattheisen… - Nature …, 2019 - nature.com
Attention deficit/hyperactivity disorder (ADHD) is a highly heritable childhood behavioral
disorder affecting 5% of children and 2.5% of adults. Common genetic variants contribute …

[HTML][HTML] A comparison of sustained-release bupropion and placebo for smoking cessation

RD Hurt, DPL Sachs, ED Glover… - … England Journal of …, 1997 - Mass Medical Soc
Background and Methods Trials of antidepressant medications for smoking cessation have
had mixed results. We conducted a double-blind, placebo-controlled trial of a sustained …