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Thomas Meitinger

ResearcherPublications, citations & collaboration network

Thomas Meitinger is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 967 works, 135,102 citations, an h-index of 171 and an i10-index of 616.

967
Works
135,102
Citations
171
h-index
616
i10-index

How has Thomas Meitinger's publication output changed over time?

ScholarIQpublication output · 2000–2018

Output grew0% over the shown period — from 1 works in 2000 to 1 in 2018.

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1
1
1
1
1
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1
1
1
2000200420072009201020112013201520162018

What are the most-cited papers on Thomas Meitinger?

ScholarIQmost cited works
Biological, clinical and population relevance of 95 loci for blood lipids
Tanya M. Teslovich, Kiran Musunuru, Albert V. Smith, Andrew C. Edmondson, Ioannis M. Stylianou, Masahiro Koseki, James P. Pirruccello, Samuli Ripatti, Daniel I. Chasman, Cristen J. Willer, Christopher T. Johansen, Sigrid W. Fouchier, Aaron Isaacs, Gina M. Peloso, Maja Barbalić, Sally L. Ricketts, Joshua C. Bis, Yurii S. Aulchenko, Guðmar Þorleifsson, Mary F. Feitosa, John C. Chambers, Marju Orho‐Melander, Olle Melander, Toby Johnson, Xiaohui Li, Xiuqing Guo, Mingyao Li, Yoon Shin Cho, Min Jin Go, Young Jin Kim, Jong‐Young Lee, Taesung Park, Kyunga Kim, Xueling Sim, Rick Twee‐Hee Ong, Damien C. Croteau‐Chonka, Leslie A. Lange, Joshua D. Smith, Kijoung Song, Jing Hua Zhao, Xin Yuan, Jian’an Luan, Claudia Lamina, Andreas Ziegler, Weihua Zhang, Robert Y.L. Zee, Alan F. Wright, Jacqueline C.M. Witteman, James F. Wilson, Gonneke Willemsen, H.‐Erich Wichmann, John B. Whitfield, Dawn Waterworth, Nicholas J. Wareham, Gérard Waeber, Péter Vollenweider, Benjamin F. Voight, Véronique Vitart, André G. Uitterlinden, Manuela Uda, Jaakko Tuomilehto, John R. Thompson, Toshiko Tanaka, Ida Surakka, Heather M. Stringham, Tim D. Spector, Nicole Soranzo, Johannes H. Smit, Juha Sinisalo, Kaisa Silander, Eric J.G. Sijbrands, Angelo Scuteri, James Scott, David Schlessinger, Serena Sanna, Veikko Salomaa, Juha Saharinen, Chiara Sabatti, Aimo Ruokonen, Igor Rudan, Lynda M. Rose, Robert Roberts, Mark J. Rieder, Bruce M. Psaty, Peter P. Pramstaller, Irene Pichler, Markus Perola, Brenda W.J.H. Penninx, Nancy L. Pedersen, Cristian Pattaro, Alex Parker, Guillaume Paré, Ben A. Oostra, Christopher J. O’Donnell, Markku S. Nieminen, Deborah A. Nickerson, Grant W. Montgomery, Thomas Meitinger, Ruth McPherson, Mark I. McCarthy
Nature. 20103,705 CitationsOPEN ACCESS
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy, Yang Luo, Arthur Gilly, Jeffrey C. Barrett, Eleftheria Zeggini, Nicole Soranzo, Klaudia Walter, Carl A. Anderson, Richard Durbin, Sayantan Das, Hyun Min Kang, Christian Fuchsberger, Alan Kwong, Laura J. Scott, Sai Chen, Michael Boehnke, Abecasis Gb, Warren Kretzschmar, Anubha Mahajan, Mark I McCarthy, Jonathan Marchini, Olivier Delaneau, Andrew R Wood, Marcus A. Tuke, Timothy Frayling, Alexander Teumer, Matthias Nauck, Petr Danecek, Kevin Sharp, Carlo Sidore, Andrea Angius, Fabio Busonero, Francesco Cucca, Nicholas J. Timpson, Laura J. Corbin, George Davey Smith, Josine L. Min, Seppo Koskinen, V Salomaa, Scott Vrieze, He Zhang, Cristen J. Willer, Jan H. Veldink, Leonard H. van den Berg, Wouter van Rheenen, Annelot M. Dekker, Ulrike Peters, Tabitha A. Harrison, Charles Kooperberg, Carlos N. Pato, Michele T. Pato, Cornelia M. van Duijn, Christopher E. Gillies, Matthew G. Sampson, Ilaria Gandin, Massimiliano Cocca, Nicola Pirastu, Paolo Gasparini, Massimo Mezzavilla, Michela Traglia, Cinzia Sala, Daniela Toniolo, Dorrett Boomsma, Kari Branham, Gerome Breen, Chad M. Brummett, Ross M. Fraser, Harry Campbell, James F. Wilson, Andrew T. Chan, Matthias Kretzler, Emily Y. Chew, Francis S. Collins, George Dedoussis, Aliki‐Eleni Farmaki, Marcus Dörr, Uwe Völker, Luigi Ferrucci, Lukas Forer, Sebastian Schoenherr, Stacey Gabriel, Palotie A, David Altshuler, Shawn Levy, R Myers, Leif Groop, Andrew Hattersley, Oddgeir L. Holmen, Kristian Hveem, James Lee, M McGue, William Iacono, Thomas Meitinger, David Melzer, Karen L Mohlke, John B Vincent, Deborah Nickerson, Melvin McInnis, J Brent Richards, Kerrin Small
S137905309. 20163,312 CitationsOPEN ACCESS
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
Alexander Zimprich, Saskia Biskup, Petra Leitner, Peter Lichtner, Matthew J. Farrer, Sarah Lincoln, Jennifer M. Kachergus, Mary Hulihan, Ryan J. Uitti, Donald B. Calne, A. Jon Stoessl, Ronald F. Pfeiffer, Nadja Patenge, Iria Carballo‐Carbajal, P. Vieregge, Friedrich Asmus, Bertram Müller‐Myhsok, Dennis W. Dickson, Thomas Meitinger, Tim M. Strom, Zbigniew K. Wszołek, Thomas Gasser
Neuron. 20043,071 CitationsOPEN ACCESS
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Majid Nikpay, Alexandre F.R. Stewart, Ruth McPherson, Anuj Goel, Theodosios Kyriakou, Christopher Grace, Shapour Jalilzadeh, Hugh Watkins, Martin Farrall, Natalie R. van Zuydam, Cecilia M Lindgren, Andrew P Morris, Erik Ingelsson, Hong‐Hee Won, Andrew Bjonnes, Richa Saxena, Tõnu Esko, Sekar Kathiresan, Leanne M Hall, Christopher P. Nelson, Thomas R Webb, Nilesh J Samani, Christina Willenborg, Jeanette Erdmann, Inke R. König, Stavroula Kanoni, Kathleen Stirrups, Panos Deloukas, Danish Saleheen, Wei Zhao, Philippe Frossard, Asif Rasheed, Maria Samue, Alison H. Goodall, Jemma C. Hopewell, King Wai Lau, Rory Collins, Robert Clarke, Lingyao Zeng, Thorsten Kessler, Christian Hengstenberg, Heribert Schunkert, Christian Gieger, Thomas Meitinger, Annette Peters, Abbas Dehghan, André Uitterlinden, Paul S. de Vries, Oscar H Franco, Albert Hofman, Maris Alver, Evelin Mihailov, Natalia Pervjakova, Andres Metspalu, Markus Perola, Sebastian M. Armasu, Mariza de Andrade, Kirsi Auro, Emmi Tikkanen, Samuli Ripatti, Daniel I Chasman, Lynda M Rose, Julie E Buring, Paul M Ridker, Shufeng Chen, Xiangfeng Lu, Xueli Yang, Laiyuan Wang, Dongfeng Gu, Ian Ford, Nora Franceschini, Stefan Gustafsson, Jie Huang, John Danesh, Shih-Jen Hwang, L Adrienne Cupples, Christopher J O'Donnell, Yun Kyoung Kim, Bok-Ghee Han, Bong-Jo Kim, Marcus E Kleber, Winfried März, Yingchang Lu, Omri Gottesman, Erwin P Bottinger, Ruth J F Loos, Leo-Pekka Lyytikäinen, Pekka J. Karhunen, Terho Lehtimäki, Alanna C Morrison, Eric Boerwinkle, Liming Qu, Elias Salfati, Thomas Quertermous, Themistocles L. Assimes, Markus Scholz, Frank Beutner, Joachim Thiery, Albert V Smith, Vilmundur Gudnason
S137905309. 20152,728 CitationsOPEN ACCESS
Transcriptome and genome sequencing uncovers functional variation in humans
Tuuli Lappalainen, Michael Sammeth, Marc R. Friedländer, Peter A.C. ’t Hoen, Jean Monlong, Manuel A. Rivas, Mar Gonzàlez-Porta, Natalja Kurbatova, Thasso Griebel, Pedro G. Ferreira, Matthias Barann, Thomas Wieland, Liliana Greger, Maarten van Iterson, Jonas Carlsson Almlöf, Paolo Ribeca, Irina Pulyakhina, Daniela Esser, Thomas Giger, Andrew Tikhonov, Marc Sultan, Gabrielle Bertier, Daniel G. MacArthur, Monkol Lek, Esther Lizano, Henk P.J. Buermans, Ismaël Padioleau, Thomas Schwarzmayr, Olof Karlberg, Halit Ongen, Helena Kilpinen, Sergi Beltrán, Marta Gut, Katja Kahlem, Vyacheslav Amstislavskiy, Oliver Stegle, Matti Pirinen, Stephen B. Montgomery, Peter Donnelly, Mark I. McCarthy, Paul Flicek, Tim M. Strom, Hans Lehrach, Stefan Schreiber, Ralf Sudbrak, Ángel Carracedo, Stylianos E. Antonarakis, Robert Häsler, Ann‐Christine Syvänen, Gert‐Jan B. van Ommen, Alvis Brāzma, Thomas Meitinger, Philip Rosenstiel, Roderic Guigó, Marta Gut, Xavier Estivill, Emmanouil T. Dermitzakis
Nature. 20132,195 CitationsOPEN ACCESS

Related on ScholarIQ

Institute of Human Genetics
Institution
Biological, clinical and population relevance of 95 loci for blood lipids
Paper
A reference panel of 64,976 haplotypes for genotype imputation
Paper
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
Paper
A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Paper
Transcriptome and genome sequencing uncovers functional variation in humans
Paper
470M+ articles · free account