Tim M. Strom

ResearcherPublications, citations & collaboration network

Tim M. Strom is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 464 works, 54,661 citations, an h-index of 111 and an i10-index of 342.

464

Works

54,661

Citations

111

h-index

342

i10-index

IDs:OpenAlex

How has Tim M. Strom's publication output changed over time?

ScholarIQpublication output · 1994–2015

Output grew0% over the shown period — from 1 works in 1994 to 1 in 2015.

199419952000200420072012201320142015

What are the most-cited papers on Tim M. Strom?

ScholarIQmost cited works

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

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, Ãngel 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

Genomewide Association Analysis of Coronary Artery Disease

Nilesh J. Samani, Jeanette Erdmann, Alistair S. Hall, Christian Hengstenberg, Massimo Mangino, Bjoern Mayer, Richard J. Dixon, Thomas Meitinger, Peter S. Braund, H. E. Wichmann, Jennifer H. Barrett, Inke R. König, Suzanne E. Stevens, Silke Szymczak, David‐Alexandre Trégouët, Mark M. Iles, Friedrich Pahlke, Helen Perlstein Pollard, Wolfgang Lieb, François Cambien, Marcus Fischer, Willem H. Ouwehand, Stefan Blankenberg, Anthony J. Balmforth, Andrea Baessler, Stephen G. Ball, Tim M. Strom, Ingrid Brænne, Christian Gieger, Panos Deloukas, Martin D. Tobin, Andreas Ziegler, John R. Thompson, Heribert Schunkert

New England Journal of Medicine. 20072,055 CitationsOPEN ACCESS

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

Kenneth E. White, W. Evans, Jeffery L.H. O'Riordan, Marcy C. Speer, Michael J. Econs, Bettina Lorenz‐Depiereux, Monika Grabowski, Thomas Meitinger, Tim M. Strom

S137905309. 20001,530 Citations

Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

Simone Rost, Andreas Fregin, Vytautas Ivaškevičius, Ernst Conzelmann, Konstanze Hörtnagel, Hans‐Joachim Pelz, Knut Tore Lappegård, E. Seifried, I. Scharrer, Edward G. D. Tuddenham, Clemens R. Müller, Tim M. Strom, Johannes Oldenburg

Nature. 20041,131 Citations

Related on ScholarIQ

TUM Klinikum

Institution

Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

Paper

Transcriptome and genome sequencing uncovers functional variation in humans

Paper

Genomewide Association Analysis of Coronary Artery Disease

Paper

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

Paper

Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

Paper