Tim M. Strom

53.7k total citations · 6 hit papers
216 papers, 16.6k citations indexed

About

Tim M. Strom is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Tim M. Strom has authored 216 papers receiving a total of 16.6k indexed citations (citations by other indexed papers that have themselves been cited), including 115 papers in Molecular Biology, 81 papers in Genetics and 25 papers in Nephrology. Recurrent topics in Tim M. Strom's work include Genomics and Rare Diseases (27 papers), Parathyroid Disorders and Treatments (23 papers) and Genetics and Neurodevelopmental Disorders (22 papers). Tim M. Strom is often cited by papers focused on Genomics and Rare Diseases (27 papers), Parathyroid Disorders and Treatments (23 papers) and Genetics and Neurodevelopmental Disorders (22 papers). Tim M. Strom collaborates with scholars based in Germany, United States and Austria. Tim M. Strom's 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 and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Tim M. Strom

213 papers receiving 16.2k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

2000 1.2k citations Michael J. Econs, Bettina Lorenz‐Depiereux et al. profile →
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

2004 857 citations Tim M. Strom et al. profile →
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita

1994 656 citations Tim M. Strom, Thomas Meitinger et al. profile →
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

2005 614 citations Gertrud Eckstein, Bettina Lorenz‐Depiereux et al. profile →
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

1994 549 citations Tim M. Strom, Thomas Meitinger et al. profile →
Mutations in the deubiquitinase gene USP8 cause Cushing's disease

2014 405 citations Thomas Meitinger, Elisabeth Graf et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Tim M. Strom Germany	63	8.0k	6.0k	3.5k	1.5k	1.5k	216	16.6k
Thomas Meitinger Germany	69	11.2k 1.4×	5.5k 0.9×	1.7k 0.5×	1.7k 1.1×	1.1k 0.8×	319	19.1k
Allen M. Spiegel United States	79	10.0k 1.2×	2.7k 0.5×	3.2k 0.9×	2.7k 1.7×	1.6k 1.1×	294	19.0k
Peter Mündel United States	74	8.3k 1.0×	3.2k 0.5×	12.8k 3.6×	1.1k 0.7×	744 0.5×	158	20.0k
Yo‐ichi Nabeshima Japan	53	4.8k 0.6×	3.1k 0.5×	3.1k 0.9×	858 0.6×	340 0.2×	117	10.1k
Thomas E. Willnow Germany	69	6.8k 0.9×	1.5k 0.3×	1.4k 0.4×	2.4k 1.6×	1.1k 0.7×	179	14.7k
Geoffrey N. Hendy Canada	59	5.2k 0.6×	2.2k 0.4×	3.5k 1.0×	402 0.3×	942 0.6×	241	10.7k
Keiichi Ozono Japan	55	4.2k 0.5×	2.3k 0.4×	1.2k 0.4×	265 0.2×	1.8k 1.2×	432	10.6k
John M. Shelton United States	75	15.7k 2.0×	2.8k 0.5×	552 0.2×	1.7k 1.1×	675 0.5×	152	22.8k
Leonard J. Deftos United States	54	3.8k 0.5×	1.0k 0.2×	1.3k 0.4×	1.1k 0.7×	1.9k 1.3×	280	10.9k
Eitan Friedman Israel	64	6.1k 0.8×	5.1k 0.9×	399 0.1×	3.1k 2.0×	949 0.6×	484	17.1k

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-authorship network of co-authors of Tim M. Strom

This figure shows the co-authorship network connecting the top 25 collaborators of Tim M. Strom. A scholar is included among the top collaborators of Tim M. Strom based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Tim M. Strom. Tim M. Strom is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Roos, Andreas, Martin Häusler, Laxmikanth Kollipara, et al.. (2024). HNRNPA1 de novo Variant Associated with Early Childhood Onset, Rapidly Progressive Generalized Myopathy. Journal of Neuromuscular Diseases. 11(5). 1131–1137. 2 indexed citations

Brunet, Theresa, Riccardo Berutti, Veronika Dill, et al.. (2022). Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Human Molecular Genetics. 31(14). 2386–2395. 4 indexed citations

Kotzaeridou, Urania, Sara K. Young, Vanessa Suckow, et al.. (2020). Novel pathogenic EIF2S3 missense variants causing clinically variable MEHMO syndrome with impaired eIF2γ translational function, and literature review. Clinical Genetics. 98(5). 507–514. 10 indexed citations

Gold, Nina B., Dong Li, Anna Chassevent, et al.. (2020). Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder. Clinical Genetics. 98(6). 571–576. 10 indexed citations

Brügger, Melanie, Theresa Brunet, Tim M. Strom, et al.. (2020). A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy. Annals of Clinical and Translational Neurology. 8(1). 278–283. 4 indexed citations

Wagner, Matias, Sarah L. Stenton, Tim M. Strom, et al.. (2020). Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases. EBioMedicine. 54. 102730–102730. 39 indexed citations

Feichtinger, René G., Michaela Brunner‐Krainz, Bader Alhaddad, et al.. (2017). Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies. Oxidative Medicine and Cellular Longevity. 2017(1). 7202589–7202589. 33 indexed citations

Said, Edith, Jessica X. Chong, Maja Hempel, et al.. (2017). Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1. American Journal of Medical Genetics Part A. 173(11). 3098–3103. 8 indexed citations

Michalakis, Stylianos, Susanne Koch, Mirko Wagner, et al.. (2013). Role of 5-hydroxymethylcytosine during postnatal retinal development. Investigative Ophthalmology & Visual Science. 54(15). 2618–2618.

10.

Sabrautzki, Sibylle, Bettina Lorenz‐Depiereux, Julia Calzada‐Wack, et al.. (2013). An ENU Mutagenesis-Derived Mouse Model with a Dominant Jak1 Mutation Resembling Phenotypes of Systemic Autoimmune Disease. American Journal Of Pathology. 183(2). 352–368. 19 indexed citations

11.

Meder, Benjamin, Jan Haas, Andreas Keller, et al.. (2011). Targeted Next-Generation Sequencing for the Molecular Genetic Diagnostics of Cardiomyopathies. Circulation Cardiovascular Genetics. 4(2). 110–122. 117 indexed citations

12.

Jamra, Rami Abou, Annick Raas‐Rothschild, Sebastian Eck, et al.. (2011). Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature. The American Journal of Human Genetics. 88(6). 788–795. 167 indexed citations

13.

Kalla, Markus, Christine Göbel, Ulrich Rothbauer, et al.. (2010). CpG-Methylation Regulates a Class of Epstein-Barr Virus Promoters. PLoS Pathogens. 6(9). e1001114–e1001114. 91 indexed citations

14.

Sharon, Dror, et al.. (2008). Identification of Novel Retinal Degeneration Loci in Consanguineous Israeli and Palestinian Families With Retinal Disease. Investigative Ophthalmology & Visual Science. 49(13). 6094–6094. 1 indexed citations

15.

Wagenstaller, Janine, Stephanie Spranger, Bettina Lorenz‐Depiereux, et al.. (2007). Copy-Number Variations Measured by Single-Nucleotide–Polymorphism Oligonucleotide Arrays in Patients with Mental Retardation. The American Journal of Human Genetics. 81(4). 768–779. 93 indexed citations

16.

Lorenz‐Depiereux, Bettina, Anna Benet‐Pagès, Gertrud Eckstein, et al.. (2006). Hereditary Hypophosphatemic Rickets with Hypercalciuria Is Caused by Mutations in the Sodium-Phosphate Cotransporter Gene SLC34A3. The American Journal of Human Genetics. 78(2). 193–201. 252 indexed citations

17.

Kato, Kentaro, Charlotte Jeanneau, Mads A. Tarp, et al.. (2006). Polypeptide GalNAc-transferase T3 and Familial Tumoral Calcinosis. Journal of Biological Chemistry. 281(27). 18370–18377. 342 indexed citations

18.

Francis, Fiona, Tim M. Strom, Steffen Hennig, et al.. (1997). Genomic Organization of the Human PEX Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets. Genome Research. 7(6). 573–585. 129 indexed citations

19.

Weil, Jochen, R. Gerzer, Tim M. Strom, et al.. (1987). Increased Plasma Cyclic Guanosine Monophosphate Concentrations in Children With High Levels of Circulating Atrial Natriuretic Peptide. PEDIATRICS. 80(4). 545–548. 10 indexed citations

20.

Gerzer, R., et al.. (1986). Mechanisms of action of atrial natriuretic factor: clinical consequences.. PubMed. 64 Suppl 6. 21–6. 14 indexed citations

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.

Explore authors with similar magnitude of impact