List of works by Jeffrey Gulcher

A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction

A Populationwide Coalescent Analysis of Icelandic Matrilineal and Patrilineal Genealogies: Evidence for a Faster Evolutionary Rate of mtDNA Lineages than Y Chromosomes ⬇️

scientific article published on April 29, 2003

A common variant associated with prostate cancer in European and African populations

scientific article published on 7 May 2006

A genetic contribution to inflammatory bowel disease in Iceland: A genealogic approach

scientific article published on 01 September 2004

A genetic risk factor for periodic limb movements in sleep

scientific article

A genome-wide study of allelic imbalance in human testicular germ cell tumors using microsatellite markers

A major susceptibility gene for asthma maps to chromosome 14q24

scientific article

A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)

scientific article (publication date: May 2004)

A population-based familial aggregation analysis indicates genetic contribution in a majority of renal cell carcinomas

scientific article

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

scientific article

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer

scientific article published on 28 October 2012

A susceptibility gene for late-onset idiopathic Parkinson's disease

article

A susceptibility gene for psoriatic arthritis maps to chromosome 16q: evidence for imprinting

scientific article published on 09 December 2002

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

scientific article (publication date: 3 April 2008)

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction

scientific article published on 10 November 2005

A whole genome association study in Icelandic multiple sclerosis patients with 4804 markers ⬇️

scientific article published on 01 October 2003

ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

scientific article

Addictions and their familiality in Iceland

scientific article

An Icelandic example of the impact of population structure on association studies

scholarly article by Agnar Helgason et al published 19 December 2004 in Nature Genetics

Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus

scientific article

Anxiety with panic disorder linked to chromosome 9q in Iceland

scientific article

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

scientific article

Association of vitamin D binding protein variants with chronic mucus hypersecretion in Iceland

scientific article published on January 2004

CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD

scientific article

Cancer as a complex phenotype: pattern of cancer distribution within and beyond the nuclear family

scientific article

Chronic mTOR activation induces a degradative smooth muscle cell phenotype

scientific article published on 01 March 2020

Comment on the phosphodiesterase 4D replication study by Bevan et al

scientific article published on 01 September 2005

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

scientific article

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

scientific journal article

Common variants conferring risk of schizophrenia

scientific article

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

scientific article published on 6 February 2009

Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

scientific article

Discovery of common variants associated with low TSH levels and thyroid cancer risk

scientific journal article

Effects of a 5-lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction: a randomized trial

scientific article published in May 2005

Endometriosis is not associated with or linked to the GALT gene

article

Endothelial ERK1/2 signaling maintains integrity of the quiescent endothelium

scientific article published on 13 June 2019

Endothelial TGF-β signalling drives vascular inflammation and atherosclerosis

scientific article published on 26 August 2019

Enhancing Retrosynthetic Reaction Prediction with Deep Learning Using Multiscale Reaction Classification

scientific article published on 01 February 2019

Erratum: Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

scholarly article published in Nature Genetics

Erratum: Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor

article

Evaluating differences in linkage disequilibrium between populations.

scientific article published in May 2010

Familial Aggregation of Parkinson's Disease in Iceland

scholarly article by Sigurlaug Sveinbjörnsdóttir et al published 14 December 2000 in The New England Journal of Medicine

Familial Risk of Lung Carcinoma in the Icelandic Population

scientific article published in The Journal of the American Medical Association

Familial predisposition and cosegregation analysis of adult obstructive sleep apnea and the sudden infant death syndrome

scientific article published in September 2002

Genes contributing to risk for common forms of stroke

scientific article

Genetic approaches to assessing evidence for a T helper type 1 cytokine defect in adult asthma

scientific article

Genetic correction of PSA values using sequence variants associated with PSA levels

scientific article published on December 2010

Genetic determinants of hair, eye and skin pigmentation in Europeans

scientific article

Genetics of gene expression and its effect on disease

scientific article (publication date: 27 March 2008)

Genetics of psoriasis in Iceland: evidence for linkage of subphenotypes to distinct Loci

scientific article

Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility

scientific article published on 20 September 2009

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

scientific article published in April 2007

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

scientific article

Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

scientific article

Genomewide Scan for Hand Osteoarthritis: A Novel Mutation in Matrilin-3 ⬇️

scientific article published on May 7, 2003

HLA-Cw6-positive and HLA-Cw6-negative patients with Psoriasis vulgaris have distinct clinical features

scientific article

In silico phenotype projection of endothelial ERK1/2 signaling

scientific article published on 12 June 2020

Large recurrent microdeletions associated with schizophrenia

scientific article

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

scientific article

Lessons from the past: familial aggregation analysis of fatal pandemic influenza (Spanish flu) in Iceland in 1918

scientific article

Linkage of essential hypertension to chromosome 18q.

scientific article

Linkage of osteoporosis to chromosome 20p12 and association to BMP2

scientific article

Localization of a gene for migraine without aura to chromosome 4q21.

scientific article

Localization of a gene for peripheral arterial occlusive disease to chromosome 1p31.

scientific article published on 06 February 2002

Localization of a susceptibility gene for common forms of stroke to 5q12

scientific article

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

scientific article

Many sequence variants affecting diversity of adult human height

scientific article published in May 2008

Microsatellite markers for linkage and association studies

scientific article published on April 2012

Multiple genetic loci for bone mineral density and fractures

scientific article published on 29 April 2008

Multiple novel transcription initiation sites for NRG1

scientific article

Mutations in BRIP1 confer high risk of ovarian cancer

scientific article

Neuregulin 1 and schizophrenia

scientific article published on January 2004

Neuregulin 1 and susceptibility to schizophrenia

scientific article

New common variants affecting susceptibility to basal cell carcinoma

scientific article

New sequence variants associated with bone mineral density

scientific article

PARK10 candidate RNF11 is expressed by vulnerable neurons and localizes to Lewy bodies in Parkinson disease brain

scientific article

PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in Sweden

scientific article published on 25 July 2007

Profiling of genes expressed in peripheral blood mononuclear cells predicts glucocorticoid sensitivity in asthma patients

scientific article

Recombination rate and reproductive success in humans

scientific article

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

article

Segmental duplication density decrease with distance to human-mouse breaks of synteny

scientific article published on 01 February 2006

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

scientific article

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

scientific article

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

scientific article

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

scientific article (publication date: February 2009)

Sequence variants in the RNF212 gene associate with genome-wide recombination rate

scientific article

Smooth Muscle Cell Reprogramming in Aortic Aneurysms

scientific article published on 01 April 2020

Strengthening the reporting of Genetic RIsk Prediction Studies (GRIPS): explanation and elaboration

scientific article published on 16 March 2011

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.

scientific article

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration

scientific article (publication date: April 2011)

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration

Support for involvement of the AHI1 locus in schizophrenia

The BARD1 Cys557Ser variant and breast cancer risk in Iceland

scientific article

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop

scientific article

The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts

scientific article

The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease

scientific article

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke

article

The gene encoding phosphodiesterase 4D confers risk of ischemic stroke

scientific article published on 21 September 2003

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

article

Two newly identified genetic determinants of pigmentation in Europeans

scientific article

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

article

Variant in the sequence of the LINGO1 gene confers risk of essential tremor

scientific journal article

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

scientific article (publication date: March 2006)

Variants conferring risk of atrial fibrillation on chromosome 4q25.

scientific article

deCODE genetics, Inc

scientific article published on 01 March 2003

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