World's Best Scientists 2026 revealed!
Award Badge
Genetics
Germany
2024
Award Badge
Genetics and Molecular Biology
Germany
2024

D-Index & Metrics

Genetics

D-Index
121
Citations
62894
World Ranking
362
National Ranking
23

Medicine

D-Index
123
Citations
64751
World Ranking
3309
National Ranking
180

Research.com Recognitions

  • 2024 - Research.com Genetics in Germany Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in Germany Leader Award
  • 2023 - Research.com Genetics in Germany Leader Award

Overview

Tim M. Strom is affiliated with the Technical University of Munich in Germany and has contributed extensively to research in the fields of Biochemistry, Genetics, and Molecular Biology, with additional work in Medicine. Their research specifically spans multiple subfields including Molecular Biology, Genetics, Neurology, Cellular and Molecular Neuroscience, and Nephrology.

Strom's scientific output includes a focus on the following main topics:

  • Genomics and Rare Diseases
  • Neurogenetic and Muscular Disorders Research
  • Neurological diseases and metabolism
  • Hereditary Neurological Disorders
  • RNA modifications and cancer
  • Mitochondrial Function and Pathology
  • Genetics and Neurodevelopmental Disorders

Key recent publications of Strom include:

  • "Monogenic variants in dystonia: an exome-wide sequencing study," 2020, The Lancet Neurology
  • "Clinical implementation of RNA sequencing for Mendelian disease diagnostics," 2022, Genome Medicine
  • "Impaired complex I repair causes recessive Leber's hereditary optic neuropathy," 2021, Journal of Clinical Investigation
  • "De novo variants in neurodevelopmental disorders-experiences from a tertiary care center," 2021, Clinical Genetics
  • "Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients," 2020, Science Advances

Frequent co-authors collaborating with Strom include:

  • Matias Wagner
  • Thomas Meitinger
  • Riccardo Berutti
  • Holger Prokisch
  • Elisabeth Graf

Strom's work has been regularly published in journals such as:

  • Brain
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Clinical Genetics
  • EBioMedicine
  • The American Journal of Human Genetics

Best Publications

  • Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology

    Alexander Zimprich;Alexander Zimprich;Saskia Biskup;Petra Leitner;Peter Lichtner

  • Genomewide association analysis of coronary artery disease.

    Nilesh J. Samani;Jeanette Erdmann;Alistair S. Hall;Christian Hengstenberg

  • Transcriptome and genome sequencing uncovers functional variation in humans

    Tuuli Lappalainen;Michael Sammeth;Marc R. Friedländer;Peter A. C. ‘t Hoen

  • Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

    Kenneth E. White;Wayne E. Evans;Jeffery L.H. O'Riordan;Marcy C. Speer

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

    Simone Rost;Andreas Fregin;Vytautas Ivaskevicius;Ernst Conzelmann

  • The genetic architecture of type 2 diabetes

    Christian Fuchsberger;Christian Fuchsberger;Jason A. Flannick;Jason A. Flannick;Tanya M. Teslovich;Anubha Mahajan

  • Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.

    Anita Rauch;Dagmar Wieczorek;Elisabeth Graf;Thomas Wieland

  • Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment

    Elisabeth B Binder;Daria Salyakina;Peter Lichtner;Gabriele M Wochnik

  • A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease

    Alexander Zimprich;Anna Benet-Pagès;Walter Struhal;Elisabeth Graf

  • Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.

    Martin Dichgans;Tobias Freilinger;Gertrud Eckstein;Elena Babini

  • An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita

    Elena Zanaria;Françoise Muscatelli;Barbara Bardoni;Tim M. Strom

  • A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets

    F. Francis;S. Hennig;B. Korn;R. Reinhardt

  • Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia

    Axel Freischmidt;Thomas Wieland;Benjamin Richter;Wolfgang Ruf

  • Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

    F Muscatelli;T M Strom;A P Walker;E Zanaria

  • Genome-wide, large-scale production of mutant mice by ENU mutagenesis

    M. H. Hrabe de Angelis;H. Flaswinkel;H. Fuchs;B. Rathkolb

  • Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

    Anneke I. den Hollander;Robert K. Koenekoop;Suzanne Yzer;Irma Lopez

  • Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy

    Paulina Navon Elkan;Sarah B. Pierce;Reeval Segel;Reeval Segel;Tom Walsh

  • An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia

    Anna Benet-Pagès;Peter Orlik;Tim M. Strom;Bettina Lorenz-Depiereux

  • Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness (DIDMOAD) Caused by Mutations in a Novel Gene (Wolframin) Coding for a Predicted Transmembrane Protein

    Tim M. Strom;Konstanze Hörtnagel;Sabine Hofmann;Florian Gekeler

  • The genetic architecture of type 2 diabetes

    Christian Fuchsberger;Jason Flannick;Tanya M. Teslovich;Anubha Mahajan

Frequent Co-Authors

Thomas Meitinger
Thomas Meitinger Technical University of Munich
Tobias B. Haack
Tobias B. Haack University of Tübingen
Holger Prokisch
Holger Prokisch Technical University of Munich
Thomas Wieland
Thomas Wieland Heidelberg University
Dagmar Wieczorek
Dagmar Wieczorek Heinrich Heine University Düsseldorf
Thomas Klopstock
Thomas Klopstock Ludwig-Maximilians-Universität München
Johannes A. Mayr
Johannes A. Mayr Paracelsus Medical University
Juliane Winkelmann
Juliane Winkelmann Technical University of Munich
Frans P.M. Cremers
Frans P.M. Cremers Radboud University
Peter Lichtner
Peter Lichtner Technical University of Munich

If you think any of the details on this page are incorrect, let us know.

Report an issue

We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:

Related Online Degrees & Career Pathways

Genetics is a versatile field that opens the door to multiple health and science careers. If you’re interested in related healthcare roles or want to advance your qualifications, several online programs may fit your goals and lifestyle.

For nurses, the flexibility of pursuing an rn to bsn online no clinicals degree allows you to earn your Bachelor of Science in Nursing without in-person clinical requirements. This is ideal for working professionals seeking upward mobility in the healthcare field.

Those aiming for advanced leadership roles in nursing may explore the fastest dnp online program options, as well as online dnp programs without dissertation, making it easier to reach the highest level of nursing practice without extensive research commitments.

For individuals seeking quick entry into allied health professions, consider medical assistant programs accelerated for a streamlined path to supporting clinical teams and learning foundational skills relevant to genetics and medical sciences.

These diverse online education options can help you build a flexible and rewarding career in genetics and related health sciences.

Best Scientists Citing Tim M. Strom

Trending Scientists

Recently Published Articles