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Author
Thomas Meitinger
also known as Andres Metspalu, H-Erich Wichmann, Martha Merrow
Broad Institute · Université de Tours · Boston University · Hebron University
About this author
Works
962
Cited by
131,425
h-index
170
i10
614
ORCID ↗
Top papers
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich, Kiran Musunuru, Albert V. Smith, et al.
·
2010
·
Nature
↗ 3,676
OA
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
Alexander Zimprich, Saskia Biskup, Petra Leitner, et al.
·
2004
·
Neuron
↗ 3,039
OA
Transcriptome and genome sequencing uncovers functional variation in humans
Tuuli Lappalainen, Michael Sammeth, Marc R. Friedländer, et al.
·
2013
·
Nature
↗ 2,172
OA
Genomewide Association Analysis of Coronary Artery Disease
Nilesh J. Samani, Jeanette Erdmann, Alistair S. Hall, et al.
·
2007
·
New England Journal of Medicine
↗ 2,048
OA
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Cardiogenics, Heribert Schunkert, Inke R. König, et al.
·
2011
·
Nature Genetics
↗ 1,940
OA
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Anubha Mahajan, Daniel Taliun, Matthias Thurner, et al.
·
2018
·
Nature Genetics
↗ 1,909
OA
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
The MAGIC investigators, Benjamin F. Voight, Laura J. Scott, et al.
·
2010
·
Nature Genetics
↗ 1,793
OA
Systematic identification of trans eQTLs as putative drivers of known disease associations
Harm-Jan Westra, Marjolein J. Peters, Tōnu Esko, et al.
·
2013
·
Nature Genetics
↗ 1,766
OA
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
Kenneth E. White, W. Evans, Jeffery L.H. O'Riordan, et al.
·
2000
·
Nature Genetics
↗ 1,522
Genome-wide association study identifies eight loci associated with blood pressure
Christopher Newton‐Cheh, Toby Johnson, Vesela Gateva, et al.
·
2009
·
Nature Genetics
↗ 1,218
OA
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets
Fiona Francis, Steffen Hennig, Bernd Korn, et al.
·
1995
·
Nature Genetics
↗ 1,112
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, et al.
·
2012
·
The Lancet
↗ 1,063
OA