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Genetics
Germany
2024
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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

Tim M. Strom publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Tim M. Strom sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 440 publications — 91st percentile

91% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Tim M. Strom D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Tim M. Strom sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 121 D-Index — 92nd percentile

92% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

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

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