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S. Pulit · SciRah

Researcher profile · Semantic Scholar

S. Pulit

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S. Pulit — researcher profile on SciRah

h-index: 42
Works: 103
Citations: 13K

Most-cited papers

Analysis of shared heritability in common disorders of the brain
V. Anttila, B. Bulik-Sullivan, H. Finucane, R. Walters +496 more
2018Science1,869 citations Open access
Semantic Scholar
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
Andrew D. Johnson, R. Handsaker, S. Pulit, Marcia M. Nizzari +2 more
2008Bioinform.1,473 citations Open access
Semantic Scholar
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
R. Malik, G. Chauhan, M. Traylor, M. Sargurupremraj +273 more
2018Nature Genetics1,441 citations Open access
Semantic Scholar
The Major Genetic Determinants of HIV-1 Control Affect HLA Class I Peptide Presentation
F. Pereyra, Xiao-Ming Jia, Paul J. McLaren, A. Telenti +333 more
2010Science1,245 citations Open access
Semantic Scholar
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry
S. Pulit, Charli Stoneman, A. Morris, A. Wood +19 more
2018bioRxiv1,050 citations Open access
Semantic Scholar
Multi-Ethnic Genome-wide Association Study for Atrial Fibrillation
C. Roselli, M. Chaffin, Lu-Chen Weng, S. Aeschbacher +214 more
2018Nature Genetics727 citations Open access
Semantic Scholar
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
W. van Rheenen, A. Shatunov, Annelot M. Dekker, R. Mclaughlin +173 more
2016Nature Genetics558 citations Open access
Semantic Scholar
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
D. Arking, S. Pulit, L. Crotti, P. van der Harst +227 more
2014Nature Genetics321 citations Open access
Semantic Scholar
GWAS identifies 14 loci for device-measured physical activity and sleep duration
A. Doherty, Karl Smith-Byrne, T. Ferreira, M. Holmes +3 more
2018Nature Communications311 citations Open access
Semantic Scholar
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Laurent C Androniki Sara L Freerk Pier Francesco Clara C P Francioli Menelaou Pulit van Dijk Palamara Elbers, L. Francioli, A. Menelaou, S. Pulit +82 more
2014Nature Genetics308 citations Open access
Semantic Scholar
The Genome of the Netherlands: design, and project goals
D. Boomsma, C. Wijmenga, E. Slagboom, M. Swertz +48 more
2013European Journal of Human Genetics289 citations Open access
Semantic Scholar
Major Histocompatibility Complex Associations of Ankylosing Spondylitis are Complex and Involve Further Epistasis with ERAP1
A. Cortes, S. Pulit, P. Leo, J. J. Pointon +44 more
2015Nature Communications271 citations Open access
Semantic Scholar
Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis
W. van Rheenen, S. Pulit, Annelot M. Dekker, A. Al Khleifat +34 more
2017European Journal of Human Genetics181 citations Open access
Semantic Scholar
Association of Granulomatosis With Polyangiitis (Wegener’s) With HLA–DPB1*04 and SEMA6A Gene Variants Evidence From Genome-Wide Analysis
G. Xie, D. Roshandel, R. Sherva, P. Monach +25 more
2013Arthritis & Rheumatism168 citations Open access
Semantic Scholar
Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease
Javier Gutierrez-Achury, A. Zhernakova, S. Pulit, G. Trynka +6 more
2015Nature Genetics155 citations Open access
Semantic Scholar
Stroke genetics: discovery, biology, and clinical applications.
M. Dichgans, S. Pulit, J. Rosand
2019Lancet Neurology154 citations Open access
Semantic Scholar
Causal relationships between obesity and the leading causes of death in women and men
Jenny C. Censin, S. Peters, Jonas Bovijn, T. Ferreira +5 more
2019PLoS Genetics154 citations Open access
Semantic Scholar
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
R. Malik, G. Chauhan, M. Traylor, M. Sargurupremraj +167 more
2018142 citations
Semantic Scholar
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
G. Chauhan, Corey R. Arnold, Audrey Y. Chu, M. Fornage +133 more
2016Lancet Neurology132 citations Open access
Semantic Scholar
A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy.
J. Kuiper, J. van Setten, S. Ripke, R. van 't Slot +21 more
2014Human Molecular Genetics131 citations Open access
Semantic Scholar
Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics
Jonas Bovijn, Kristi Krebs, Chia-Yen Chen, R. Boxall +16 more
2020Science Translational Medicine109 citations Open access
Semantic Scholar
Low-frequency and common genetic variation in ischemic stroke
R. Malik, M. Traylor, S. Pulit, S. Bevan +45 more
2016Neurology107 citations Open access
Semantic Scholar
GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology
Jonas Bovijn, Leigh Jackson, Jenny C. Censin, Chia-Yen Chen +18 more
2018American Journal of Human Genetics104 citations Open access
Semantic Scholar
Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT.
N. Nicolaou, S. Pulit, I. Nijman, G. Monroe +20 more
2016Kidney International103 citations Open access
Semantic Scholar
Negative selection in humans and fruit flies involves synergistic epistasis
M. Sohail, O. Vakhrusheva, J. Sul, S. Pulit +8 more
2016Science90 citations Open access
Semantic Scholar
Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping
C. Vermeulen, G. Geeven, Elzo de Wit, Marjon J. A. M. Verstegen +19 more
2017American Journal of Human Genetics83 citations Open access
Semantic Scholar
A comprehensive evaluation of the genetic architecture of sudden cardiac arrest
Foram N. Ashar, Rebecca N. Mitchell, C. Albert, C. Newton-Cheh +60 more
2018European Heart Journal78 citations Open access
Semantic Scholar
Genetic Variation at 16q24.2 is associated with small vessel stroke
M. Traylor, R. Malik, M. Nalls, Ioana Cotlarciuc +63 more
2017Annals of Neurology77 citations Open access
Semantic Scholar
The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public
R. V. D. van der Spek, W. van Rheenen, S. Pulit, K. Kenna +2 more
2019Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration76 citations Open access
Semantic Scholar
An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval.
A. Kapoor, Rajesh B. Sekar, N. Hansen, K. Fox‐Talbot +18 more
2014American Journal of Human Genetics74 citations Open access
Semantic Scholar
Deleterious Alleles in the Human Genome Are on Average Younger Than Neutral Alleles of the Same Frequency
Adam Kiezun, S. Pulit, L. Francioli, F. van Dijk +8 more
2013PLoS Genetics74 citations Open access
Semantic Scholar
Resetting the bar: Statistical significance in whole‐genome sequencing‐based association studies of global populations
S. Pulit, Sera A. J. de With, P. D. de Bakker
2017Genetic Epidemiology73 citations Open access
Semantic Scholar
Sexual dimorphisms in genetic loci linked to body fat distribution
S. Pulit, T. Karaderi, C. Lindgren
2017Bioscience Reports71 citations Open access
Semantic Scholar
COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls
K. Rannikmäe, Vhinoth Sivakumaran, H. Millar, R. Malik +24 more
2017Neurology70 citations Open access
Semantic Scholar
Estimating the Net Contribution of Interleukin-28B Variation to Spontaneous Hepatitis C Virus Clearance
J. di Iulio, A. Ciuffi, Karen Fitzmaurice, D. Kelleher +14 more
2011Hepatology67 citations Open access
Semantic Scholar
Multiethnic Genetic Association Studies Improve Power for Locus Discovery
S. Pulit, B. Voight, P. D. de Bakker
2010PLoS ONE64 citations Open access
Semantic Scholar
Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis
J. Kuiper, J. van Setten, M. Devall, M. Cretu-Stancu +17 more
2018bioRxiv56 citations Open access
Semantic Scholar
Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels
E. V. van Leeuwen, L. Karssen, J. Deelen, A. Isaacs +68 more
2015Nature Communications56 citations Open access
Semantic Scholar
Serum magnesium and calcium levels in relation to ischemic stroke
S. Larsson, M. Traylor, S. Burgess, G. Boncoraglio +255 more
2019Neurology46 citations Open access
Semantic Scholar
Identification of an Amino Acid Motif in HLA–DRβ1 That Distinguishes Uveitis in Patients With Juvenile Idiopathic Arthritis
A. Haasnoot, M. Schilham, S. Kamphuis, P. Hissink Muller +30 more
2018Arthritis & Rheumatology44 citations Open access
Semantic Scholar
Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes
S. Pulit, Lu-Chen Weng, P. McArdle, L. Trinquart +9 more
2018Neurology: Genetics42 citations Open access
Semantic Scholar
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk
Bing Yu, S. Pulit, Shih-Jen Hwang, J. Brody +31 more
2015Circulation: Cardiovascular Genetics42 citations Open access
Semantic Scholar
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
R. Malik, G. Chauhan, M. Traylor, M. Sargurupremraj +273 more
2019Nature Genetics40 citations Open access
Semantic Scholar
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort
Gijs H. P. Tazelaar, Annelot M. Dekker, Joke J. F. A. van Vugt, R. V. D. van der Spek +26 more
2018Neurobiology of Aging36 citations Open access
Semantic Scholar
Novel Loci Associated with Increased Risk of Sudden Cardiac Death in the Context of Coronary Artery Disease
A. Huertas-Vazquez, C. Nelson, Xiu-Qing Guo, K. Reinier +20 more
2013PLoS ONE36 citations Open access
Semantic Scholar
Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting
G. Chauhan, H. Adams, C. Satizabal, Joshua C. Bis +146 more
2019Neurology33 citations Open access
Semantic Scholar
Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN)
B. Mitchell, M. Fornage, P. McArdle, Yu-Ching Cheng +10 more
2014Frontiers in Genetics33 citations Open access
Semantic Scholar
Colocalization of Gene Expression and DNA Methylation with Genetic Risk Variants Supports Functional Roles of MUC5B and DSP in Idiopathic Pulmonary Fibrosis.
R. Borie, J. Cardwell, I. Konigsberg, Camille M. Moore +20 more
2022American Journal of Respiratory and Critical Care Medicine32 citations Open access
Semantic Scholar
CHCHD10 variants in Amyotrophic Lateral Sclerosis: where is the evidence?
Gijs H. P. Tazelaar, W. van Rheenen, S. Pulit, R. V. D. van der Spek +30 more
2018Annals of Neurology30 citations Open access
Semantic Scholar
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis
Annelot M. Dekker, F. Diekstra, S. Pulit, Gijs H. P. Tazelaar +16 more
2019Scientific Reports29 citations Open access
Semantic Scholar

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