Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

J. Eicher · SciRah

Researcher profile · Semantic Scholar

J. Eicher

Share profile

J. Eicher — researcher profile on SciRah

h-index: 37
Works: 77
Citations: 6,748

Most-cited papers

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
R. Scott, L. Scott, R. Mägi, L. Marullo +171 more
2017Diabetes684 citations Open access
Semantic Scholar
Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistance
L. Lotta, P. Gulati, F. Day, F. Payne +26 more
2016Nature Genetics545 citations Open access
Semantic Scholar
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
A. Nicolas, K. Kenna, A. Renton, N. Ticozzi +200 more
2018Neuron409 citations Open access
Semantic Scholar
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
George B. Ehret, T. Ferreira, D. Chasman, A. Jackson +309 more
2016Nature Genetics403 citations Open access
Semantic Scholar
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
R. Chia, M. Sabir, S. Bandres-Ciga, S. Saez-Atienzar +151 more
2021Nature Genetics373 citations Open access
Semantic Scholar
Fifteen new risk loci for coronary artery disease highlight arterial wall-specific mechanisms
J. Howson, Wei Zhao, D. Barnes, W. Ho +68 more
2017Nature Genetics291 citations Open access
Semantic Scholar
Large-scale genomic analyses link reproductive ageing to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
F. Day, K. Ruth, D. Thompson, Kathryn L. Lunetta +237 more
2015Nature Genetics284 citations Open access
Semantic Scholar
Genetic architecture of subcortical brain structures in 38,851 individuals
C. Satizabal, H. Adams, D. Hibar, Charles C. White +285 more
2019Nature Genetics250 citations Open access
Semantic Scholar
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Thomas R. Webb, J. Erdmann, K. Stirrups, N. Stitziel +130 more
2017Journal of the American College of Cardiology246 citations Open access
Semantic Scholar
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study
R. Guerreiro, O. Ross, Célia Kun-Rodrigues, D. Hernandez +61 more
2017Lancet Neurology244 citations Open access
Semantic Scholar
Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults
M. Graff, R. Scott, A. Justice, Kristin L. Young +277 more
2017PLoS Genetics204 citations Open access
Semantic Scholar
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci
Gregory T. Jones, G. Tromp, H. Kuivaniemi, S. Gretarsdottir +113 more
2017Circulation Research180 citations Open access
Semantic Scholar
Genetic architecture of human plasma lipidome and its link to cardiovascular disease
Rubina Tabassum, Joel T. Rämö, P. Ripatti, J. Koskela +255 more
2019Nature Communications167 citations Open access
Semantic Scholar
The additive blood pressure lowering effects of exercise intensity on post-exercise hypotension.
J. Eicher, C. Maresh, G. Tsongalis, P. Thompson +1 more
2010American Heart Journal163 citations
Semantic Scholar
GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes
J. Eicher, C. Landowski, Brian Stackhouse, Arielle Sloan +5 more
2014Nucleic Acids Res.156 citations Open access
Semantic Scholar
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis
S. Bandres-Ciga, A. Noyce, G. Hemani, A. Nicolas +156 more
2019Annals of Neurology140 citations Open access
Semantic Scholar
Characterization of the platelet transcriptome by RNA sequencing in patients with acute myocardial infarction
J. Eicher, Y. Wakabayashi, O. Vitseva, N. Esa +5 more
2015Platelets137 citations Open access
Semantic Scholar
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels
M. Sabater-Lleal, J. Huffman, P. D. de Vries, J. Marten +72 more
2019Circulation128 citations Open access
Semantic Scholar
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation
Audrey Y. Chu, Xuan Deng, Virginia Fisher, A. Drong +64 more
2016Nature Genetics124 citations Open access
Semantic Scholar
Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease
Ci Song, S. Burgess, J. Eicher, C. O'Donnell +1 more
2017Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease110 citations Open access
Semantic Scholar
Genome-Wide Association Study of Shared Components of Reading Disability and Language Impairment
J. Eicher, Natalie R. Powers, L. Miller, N. Akshoomoff +26 more
2013Genes, Brain and Behavior110 citations Open access
Semantic Scholar
Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-wide Association Studies
A. Joshi, C. Andersson, S. Buch, S. Stender +51 more
2016Gastroenterology101 citations Open access
Semantic Scholar
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.
J. Eicher, Nathalie Chami, T. Kacprowski, A. Nomura +109 more
2016American Journal of Human Genetics89 citations Open access
Semantic Scholar
Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.
Natalie R. Powers, J. Eicher, F. Butter, Y. Kong +4 more
2013American Journal of Human Genetics80 citations Open access
Semantic Scholar
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.
Nathalie Chami, Ming-Huei Chen, A. J. Slater, J. Eicher +109 more
2016American Journal of Human Genetics77 citations Open access
Semantic Scholar
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis
Janel O. Johnson, Ruth Chia, Danny E. Miller, Rachel Li +286 more
2021JAMA Neurology70 citations Open access
Semantic Scholar
Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability
N. Cope, J. Eicher, H. Meng, C. Gibson +6 more
2012NeuroImage62 citations Open access
Semantic Scholar
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.
Salman M. Tajuddin, U. Schick, J. Eicher, Nathalie Chami +93 more
2016American Journal of Human Genetics60 citations Open access
Semantic Scholar
Imaging-Genetics in Dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments
J. Eicher, J. Gruen
2013Molecular Genetics and Metabolism59 citations Open access
Semantic Scholar
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin.
Ching-Ti Liu, Sridharan Raghavan, Nisa M. Maruthur, E. Kabagambe +111 more
2016American Journal of Human Genetics58 citations Open access
Semantic Scholar
Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits
N. Pankratz, U. Schick, Yi Zhou, Wei Zhou +77 more
2016Nature Genetics57 citations Open access
Semantic Scholar
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
Amy M. Matteini, Toshiko Tanaka, D. Karasik, G. Atzmon +63 more
2016Aging Cell56 citations Open access
Semantic Scholar
SPECIAL REVIEW: PLATELETS AT THE HEART OF THERAPY The genetics of platelet count and volume in humans
J. Eicher, G. Lettre, Andrew D. Johnson
201850 citations
Semantic Scholar
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ
J. Eicher, Natalie R. Powers, L. Miller, K. Mueller +10 more
2014Human Genetics46 citations Open access
Semantic Scholar
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
Erik L. Bao, Satish K. Nandakumar, Xiaotian Liao, A. Bick +335 more
2020Nature44 citations Open access
Semantic Scholar
Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders
J. Eicher, J. Gruen
2014Autism Research43 citations Open access
Semantic Scholar
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology.
P. D. de Vries, M. Sabater-Lleal, J. Huffman, J. Marten +41 more
2019Blood40 citations Open access
Semantic Scholar
The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles
Natalie R. Powers, J. Eicher, L. Miller, Y. Kong +6 more
2015Journal of Medical Genetics37 citations Open access
Semantic Scholar
Heritability and genetic variance of dementia with Lewy bodies
R. Guerreiro, V. Escott-Price, D. Hernandez, Célia Kun-Rodrigues +66 more
2018bioRxiv36 citations Open access
Semantic Scholar
Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide
C. Satizabal, H. Adams, D. Hibar, Charles C. White +281 more
201731 citations Open access
Semantic Scholar
Replication and hematological characterization of human platelet reactivity genetic associations in men from the Caerphilly Prospective Study (CaPS)
J. Eicher, L. Xue, Y. Ben-Shlomo, A. Beswick +1 more
2016Journal of Thrombosis and Thrombolysis31 citations Open access
Semantic Scholar
Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children
J. Eicher, Angela M. Montgomery, N. Akshoomoff, D. Amaral +22 more
2015Brain Imaging and Behavior30 citations Open access
Semantic Scholar
The promises and challenges of the use of genomics in the prescription of exercise for hypertension: the 2013 update.
Garrett I. Ash, J. Eicher, L. Pescatello
2013Current hypertension reviews30 citations
Semantic Scholar
Associations of Prenatal Nicotine Exposure and the Dopamine Related Genes ANKK1 and DRD2 to Verbal Language
J. Eicher, Natalie R. Powers, Kelly Cho, L. Miller +4 more
2013PLoS ONE29 citations Open access
Semantic Scholar
The complex genetics of gait speed: genome-wide meta-analysis approach
Dan Ben-Avraham, D. Karasik, Joe Verghese, K. Lunetta +66 more
2017Aging28 citations Open access
Semantic Scholar
Large-scale pharmacogenomic study of sulfonylureas and the QT, JT, and QRS intervals: CHARGE Pharmacogenomics Working Group
James S. Floyd, C. Sitlani, C. Avery, R. Noordam +55 more
2016The Pharmacogenomics Journal19 citations Open access
Semantic Scholar
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata
E. Sliz, J. Tyrmi, N. Rahmioglu, K. Zondervan +323 more
2023Nature Communications18 citations Open access
Semantic Scholar
A comprehensive screening of copy number variability in dementia with Lewy bodies
Célia Kun-Rodrigues, Tatiana Orme, Susana Carmona, D. Hernandez +64 more
2018Neurobiology of Aging18 citations Open access
Semantic Scholar
Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals
Richard Ågren, S. Patil, Xiang Zhou, A. Palotie +325 more
2023Molecular biology and evolution17 citations Open access
Semantic Scholar
Exome-Chip Meta-Analysis Identifies Association between Variation in ANKRD26 and Platelet Aggregation
Ming-Huei Chen, L. Yanek, J. Backman, J. Eicher +12 more
2017Platelets17 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

Andrew D. Johnson×23
Invite
Andrew D. Johnson — researcher profile on SciRah
A. Smith×13
Invite
A. Smith — researcher profile on SciRah
P. Tienari×12
Invite
P. Tienari — researcher profile on SciRah
V. Gudnason×12
Invite
V. Gudnason — researcher profile on SciRah

×11

Invite

L. Launer — researcher profile on SciRah

A. Uitterlinden×11

Invite

A. Uitterlinden — researcher profile on SciRah

Invite

M. Nalls — researcher profile on SciRah

Invite

M. Fornage — researcher profile on SciRah

M. Kähönen×10

Invite

M. Kähönen — researcher profile on SciRah

Yong-Mei Liu×10

Invite

Yong-Mei Liu — researcher profile on SciRah

Invite

J. Rotter — researcher profile on SciRah

Invite

T. Harris — researcher profile on SciRah