Tim M. Strom

54.3k citations

217 papers · 16.9k · 5 hit papers · h-index 63

Impact in

Nephrology top 0.05%
- Parathyroid Disorders and Treatments
Genetics top 0.1%
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders

Papers in

Molecular Biology 103
- Mitochondrial Function and Pathology 18
- Retinal Development and Disorders 11
- RNA modifications and cancer 11
Genetics 70
- Genomics and Rare Diseases 22
- Genetics and Neurodevelopmental Disorders 19
- Genomic variations and chromosomal abnormalities 15

Co-authors: Thomas Meitinger (73 shared papers)Bettina Lorenz‐Depiereux (25 shared papers)Anna Benet‐Pagès (13 shared papers)Michael J. Econs (9 shared papers)Kenneth E. White (5 shared papers)Monika Grabowski (3 shared papers)W. Evans (2 shared papers)Marcy C. Speer (2 shared papers)
Journals: European Journal of Human Genetics (16 papers)The American Journal of Human Genetics (16 papers)Nature Genetics (8 papers)Human Molecular Genetics (7 papers)Clinical Genetics (7 papers)
Partner nations: Germany United States Austria

In The Last Decade

Tim M. Strom

214 papers receiving 16.6k citations

Tim M. Strom's Hit Papers

5 papers align trajectories log scale

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine 2005 · 619 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2005 The Lancet
2004 Nature
2000 Nature Genetics
1994 Nature
1994 Nature

Peers

Countries citing papers authored by Tim M. Strom

Since Specialization

Citations

This map shows the geographic impact of Tim M. Strom's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Tim M. Strom with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tim M. Strom more than expected).

Fields of papers citing papers by Tim M. Strom

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tim M. Strom. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Tim M. Strom. The network helps show where Tim M. Strom may publish in the future.

Co-authors

The 25 scholars most cited alongside Tim M. Strom, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Tim M. Strom Line = papers co-authored together Tim M. Strom links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 217 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23 Nature Genetics ·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 Hit paper breakdown →	2000	1160
2	Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2 Nature ·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 Hit paper breakdown →	2004	858
3	An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita Nature ·Elena Zanaria, Françoise Muscatelli, Barbara Bardoni, Tim M. Strom, Silvana Guioli, Weiwen Guo, Enzo Lalli, Claudio Moser, Ann P. Walker, Edward R.B. McCabe, Thomas Meitinger, Anthony P. Monaco, Paolo Sassone‐Corsi, Giovanna Camerino Hit paper breakdown →	1994	658
4	Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine The Lancet ·Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz‐Depiereux, Saskia Biskup, Michel D. Ferrari, Jürgen Herzog, Arn M. J. M. van den Maagdenberg, Michael Pusch, Tim M. Strom Hit paper breakdown →	2005	619
5	Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism Nature ·Françoise Muscatelli, Tim M. Strom, Ann P. Walker, Elena Zanaria, Dominique Récan, Alfons Meindl, Barbara Bardoni, Silvana Guioli, Günther Zehetner, Wolfgang Rabl, Hans Peter Schwarz, Jean‐Claude Kaplan, Giovanna Camerino, Thomas Meitinger, Anthony P. Monaco Hit paper breakdown →	1994	551
6	Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis The American Journal of Human Genetics ·Anneke I. den Hollander, Robert K. Koenekoop, Suzanne Yzer, Irma López, Maarten Arends, Krysta Voesenek, Marijke N. Zonneveld, Tim M. Strom, Thomas Meitinger, Han G. Brunner, Carel B. Hoyng, L. Ingeborgh van den Born, Klaus Rohrschneider, Frans P.M. Cremers	2006	491
7	Mutations in the deubiquitinase gene USP8 cause Cushing's disease Nature Genetics ·Martín Reincke, Silviu Sbiera, Akira Hayakawa, Marily Theodoropoulou, Andrea Oßwald, Felix Beuschlein, Thomas Meitinger, Emi Mizuno-Yamasaki, Kohei Kawaguchi, Yasushi Saeki, Keiji Tanaka, Thomas Wieland, Elisabeth Graf, Wolfgang Saeger, Cristina L. Ronchi, Bruno Allolio, Michael Buchfelder, Tim M. Strom, Martin Faßnacht, Masayuki Komada	2014	413
8	Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23 Kidney International ·Kenneth E. White, Gwénaëlle Carn, Bettina Lorenz‐Depiereux, Anna Benet‐Pagès, Tim M. Strom, Michael J. Econs	2001	386
9	DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis Nature Genetics ·Bettina Lorenz‐Depiereux, Murat Bastepe, Anna Benet‐Pagès, Mustapha Amyere, Janine Wagenstaller, Ursula Müller-Barth, Klaus Badenhoop, Stéphanie Kaiser, Roger S. Rittmaster, Alan H Shlossberg, José L. Olivares, C Loris, Feliciano J. Ramos, Francis H. Glorieux, Miikka Vikkula, Harald Jüppner, Tim M. Strom	2006	377
10	An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia Human Molecular Genetics ·Anna Benet‐Pagès, Peter Orlik, Tim M. Strom, Bettina Lorenz‐Depiereux	2004	374
11	Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein Human Molecular Genetics ·Tim M. Strom	1998	371
12	An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness Nature Genetics ·Tim M. Strom, Gerald Nyakatura, Eckart Apfelstedt-Sylla, Heide Hellebrand, Birgit Lorenz, Bernhard H. F. Weber, Krisztina Wutz, Nadja Gutwillinger, Klaus Rüther, Bernd Drescher, Christian Sauer, Eberhart Zrenner, Thomas Meitinger, André Rosenthal, Alfons Meindl	1998	369
13	Polypeptide GalNAc-transferase T3 and Familial Tumoral Calcinosis Journal of Biological Chemistry ·Kentaro Kato, Charlotte Jeanneau, Mads A. Tarp, Anna Benet‐Pagès, Bettina Lorenz‐Depiereux, Eric Bennett, Ulla Mandel, Tim M. Strom, Henrik Clausen	2006	344
14	Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome Nature Genetics ·Alexander Zimprich, Monika Grabowski, Friedrich Asmus, Markus Naumann, Daniela Berg, Markus Bertram, K H Scheidtmann, Peter Kern, Juliane Winkelmann, Bertram Müller‐Myhsok, Leonhard Riedel, Matthias Bauer, Tanja R. Müller, Mirna Castro, Thomas Meitinger, Tim M. Strom, Thomas Gasser	2001	313
15	Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets The American Journal of Human Genetics ·Bettina Lorenz‐Depiereux, Dirk Schnabel, Dov Tiosano, Gabriele Häusler, Tim M. Strom	2010	265
16	Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3 The American Journal of Human Genetics ·Bettina Lorenz‐Depiereux, Anna Benet‐Pagès, Gertrud Eckstein, Yardena Tenenbaum‐Rakover, Janine Wagenstaller, Dov Tiosano, Ruth Gershoni‐Baruch, Norbert Albers, Peter Lichtner, Dirk Schnabel, Ze’ev Hochberg, Tim M. Strom	2006	254
17	The Autosomal Dominant Hypophosphatemic Rickets (ADHR) Gene Is a Secreted Polypeptide Overexpressed by Tumors that Cause Phosphate Wasting The Journal of Clinical Endocrinology & Metabolism ·Kenneth E. White, Kenneth B. Jonsson, Gwénaëlle Carn, Geeta Hampson, Tim D. Spector, Michael Mannstadt, Bettina Lorenz‐Depiereux, Akimitsu Miyauchi, In Myung Yang, Östen Ljunggren, Thomas Meitinger, Tim M. Strom, Harald Jüppner, Michael J. Econs	2001	232
18	A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation Nature Genetics ·Alain Carrié, Jun Li, T Bienvenu, Marie Claude Vinet, Nathalie McDonell, Philippe Couvert, Ramzi Zemni, (unknown), G.J.C.M. van Buggenhout, Suzanna G.M. Frints, Ben C.J. Hamel, Claude Moraine, Hans Hilger Ropers, Tim M. Strom, Gareth R. Howell, (unknown), Mark Ross, A Kahn, J. P. Fryns, C. Beldjord, Peter Marynen, Jamel Chelly	1999	226
19	Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis Nature Genetics ·Víctor L. Ruiz‐Pérez, Susan Ide, Tim M. Strom, Bettina Lorenz, David I. Wilson, Kathryn Woods‐Townsend, Lynn King, Clair A. Francomano, Peter Freisinger, Stephanie Spranger, Bruno Marino, Bruno Dallapiccola, Michael Wright, Thomas Meitinger, Mihael H. Polymeropoulos, Judith Goodship	2000	225
20	A powerful tool for genome analysis in maize: development and evaluation of the high density 600 k SNP genotyping array BMC Genomics ·Sandra Unterseer, Eva Bauer, Georg Haberer, Michael Seidel, Carsten Knaak, Milena Ouzunova, Thomas Meitinger, Tim M. Strom, Ruedi Fries, Hubert Pausch, Christofer Bertani, Alessandro Davassi, Klaus Mayer, Chris‐Carolin Schön	2014	203

About Tim M. Strom

Tim M. Strom is a scholar working on Molecular Biology, Genetics, Nephrology, Cellular and Molecular Neuroscience and Cell Biology, having authored 217 papers that have together received 16.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (22 papers), Parathyroid Disorders and Treatments (22 papers), Genetics and Neurodevelopmental Disorders (19 papers), Mitochondrial Function and Pathology (18 papers), Genomic variations and chromosomal abnormalities (15 papers), Retinal Development and Disorders (11 papers), RNA modifications and cancer (11 papers) and Neurological diseases and metabolism (10 papers). The work is most often cited by research in Nephrology (3.5k citations), Genetics (5.4k citations), Molecular Biology (7.4k citations), Rheumatology (1.2k citations) and Endocrinology, Diabetes and Metabolism (1.3k citations). Tim M. Strom has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Thomas Meitinger, Bettina Lorenz‐Depiereux, Anna Benet‐Pagès, Michael J. Econs, Kenneth E. White, Monika Grabowski, W. Evans, Marcy C. Speer, Barbara Bardoni and Peter Orlik. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Nature Genetics, Human Molecular Genetics and Clinical Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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Tim M. Strom

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In The Last Decade

Tim M. Strom

Tim M. Strom's Hit Papers

Peers

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Fields of papers citing papers by Tim M. Strom

All Works

About Tim M. Strom

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