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U. Schick · SciRah

Researcher profile · Semantic Scholar

U. Schick

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U. Schick — researcher profile on SciRah

h-index: 26
Works: 41
Citations: 2,821

Most-cited papers

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
N. Stitziel, K. Stirrups, Nicholas G. D. Masca, J. Erdmann +125 more
2016New England Journal of Medicine439 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
Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease
N. Stitziel, H. Won, A. Morrison, G. Peloso +72 more
2014New England Journal of Medicine253 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
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels
Tuomas O. Kilpeläinen, Jayne F. Martin Carli, Alicja A. Skowronski, Qi Sun +173 more
2016Nature Communications144 citations Open access
Semantic Scholar
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits
P. Auer, A. Teumer, U. Schick, A. O'Shaughnessy +22 more
2014Nature Genetics139 citations Open access
Semantic Scholar
Interleukin-6 Signaling Effects on Ischemic Stroke and other Cardiovascular Outcomes: A Mendelian Randomization Study
Marios K. Georgakis, R. Malik, D. Gill, N. Franceschini +109 more
2020Circulation Genomic and Precision Medicine119 citations Open access
Semantic Scholar
Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities
L. O. Huang, A. Rauch, Eugenia Mazzaferro, Michael H. Preuss +12 more
2021Nature Metabolism105 citations
Semantic Scholar
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
N. Stitziel, K. Stirrups, N. Masca, J. Erdmann +125 more
2016New England Journal of Medicine96 citations
Semantic Scholar
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits
A. Macé, M. Tuke, Patrick Deelen, K. Kristiansson +102 more
2017Nature Communications90 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
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.
U. Schick, D. Jain, C. Hodonsky, J. Morrison +34 more
2016American Journal of Human Genetics78 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
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.
Zhao Chen, Hua Tang, R. Qayyum, U. Schick +32 more
2013Human Molecular Genetics72 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
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
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.
F. V. van Rooij, R. Qayyum, A. Smith, Yi Zhou +96 more
2017American Journal of Human Genetics52 citations Open access
Semantic Scholar
SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.
Man Li, Yong Li, Olivia Weeks, Vladan Mijatovic +152 more
2017Journal of the American Society of Nephrology49 citations Open access
Semantic Scholar
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos
C. Hodonsky, D. Jain, U. Schick, J. Morrison +23 more
2017PLoS Genetics49 citations Open access
Semantic Scholar
Rare coding variants and X-linked loci associated with age at menarche
K. Lunetta, F. Day, P. Sulem, K. Ruth +117 more
2015Nature Communications49 citations Open access
Semantic Scholar
Association of exome sequences with plasma C-reactive protein levels in >9000 participants.
U. Schick, P. Auer, J. Bis, Hong-Huang Lin +40 more
2015Human Molecular Genetics47 citations Open access
Semantic Scholar
Rare, low frequency, and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans
Emily Olfson, N. Saccone, Eric O. Johnson, Li-Shiun Chen +49 more
2015Molecular Psychiatry44 citations Open access
Semantic Scholar
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
L. Polfus, R. Khajuria, U. Schick, N. Pankratz +52 more
2016American Journal of Human Genetics41 citations Open access
Semantic Scholar
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos
D. Jain, C. Hodonsky, U. Schick, J. Morrison +17 more
2017Human Molecular Genetics36 citations Open access
Semantic Scholar
Confirmation of the Reported Association of Clonal Chromosomal Mosaicism with an Increased Risk of Incident Hematologic Cancer
U. Schick, A. McDavid, P. Crane, Noah Weston +14 more
2013PLoS ONE34 citations Open access
Semantic Scholar
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
L. Polfus, R. Khajuria, U. Schick, N. Pankratz +52 more
2016American Journal of Human Genetics31 citations Open access
Semantic Scholar
Generation Scotland
K. Lunetta, F. Day, P. Sulem, K. Ruth +81 more
201514 citations
Semantic Scholar
Risk Factors Associated With Epidural Use
Samuel M. Lancaster, U. Schick, Morwan M. Osman, D. Enquobahrie
2012Journal of Clinical Medicine Research12 citations Open access
Semantic Scholar
Generalization and fine mapping of red blood cell trait genetic associations to multi-ethnic populations: The PAGE Study
Chani Jo Hodonsky, C. Schurmann, U. Schick, Jonathan M. Kocarnik +14 more
2018American journal of hematology/oncology7 citations Open access
Semantic Scholar
Erratum: Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis (American Journal of Human Genetics (2016) 99(2) (481–488)(S0002929716302208)(10.1016/j.ajhg.2016.06.016))
L. Polfus, R. Khajuria, U. Schick, N. Pankratz +52 more
20167 citations Open access
Semantic Scholar
Premature menopause genome-wide association study in 75,000 women of European ancestry
G. Galarneau, P. Fontanillas, T. Hu-Seliger, C. Clementi +5 more
2018Fertility and Sterility2 citations Open access
Semantic Scholar
Correction: Risk Factors Associated With Epidural Use
Samuel M. Lancaster, U. Schick, Morwan M. Osman, D. Enquobahrie
2016Journal of Clinical Medicine Research1 citations Open access
Semantic Scholar
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With€Coronary Artery€Disease
Thomas R. Webb, Jeanette Erdmann, K. Stirrups, N. Stitziel +85 more
1 citations
Semantic Scholar
Expanded carrier screening reveals insights into enrichment of specific disorders within a reproductive genomic space
L. Hurd, U. Schick, J. Hayes, J. Olberding +3 more
20170 citations Open access
Semantic Scholar
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease (vol 374, pg 1134, 2016, Correction)
N. Stitziel, K. Stirrups, N. Masca, J. Erdmann +125 more
20160 citations
Semantic Scholar
Abstract P256: Generalization and Fine Mapping of Genetic Associations with Hematocrit in Multi-ethnic Populations: The Population Architecture Using Genomics and Epidemiology (PAGE) Study
C. Hodonsky, U. Schick, Jonathan M. Kocarnik, C. Schurmann +11 more
20160 citations
Semantic Scholar
Corrigendum: Rare coding variants and X-linked loci associated with age at menarche
K. Lunetta, F. Day, P. Sulem, K. Ruth +82 more
2015Nature Communications0 citations Open access
Semantic Scholar
Abstract P358: Discovery Loci and Generalization of Platelet Count Associations in the Hispanic Community Health Study: Study of Latinos (HCHS/SoL)
C. Hodonsky, U. Schick, J. Morrison, C. Laurie +4 more
20150 citations
Semantic Scholar
Large-Scale Genetic Analyses of Inflammatory Traits and Hematologic Parameters: Insights and Implications
U. Schick
20150 citations
Semantic Scholar
Chromosomal karyotype abnormalities are associated with increased risk of hematologic malignancies
U. Schick
20120 citations
Semantic Scholar
University of Dundee Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Tom R. Webb, J. Erdmann, K. Stirrups, N. Stitziel +34 more
0 citations
Semantic Scholar

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