# Tim M. Strom

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/tim-m-strom/

## Facts

| Field | Value |
| --- | --- |
| Citations | 54,661 |
| Field | Genomics and Rare Diseases |
| h-index | 111 |
| i10-index | 342 |
| Last Known Institution | TUM Klinikum |
| OpenAlex ID | https://openalex.org/A5110219194 |
| Works | 464 |

## Researcher papers

Showing 12 of 20.

- [Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology](https://scholariq.org/papers/mutations-in-lrrk2-cause-autosomal-dominant-parkinsonism-with-pleomorphic/)
- [Transcriptome and genome sequencing uncovers functional variation in humans](https://scholariq.org/papers/transcriptome-and-genome-sequencing-uncovers-functional-variation-in-humans/)
- [Genomewide Association Analysis of Coronary Artery Disease](https://scholariq.org/papers/genomewide-association-analysis-of-coronary-artery-disease/)
- [Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23](https://scholariq.org/papers/autosomal-dominant-hypophosphataemic-rickets-is-associated-with-mutations-in/)
- [Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2](https://scholariq.org/papers/mutations-in-vkorc1-cause-warfarin-resistance-and-multiple-coagulation-factor/)
- [A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets](https://scholariq.org/papers/a-gene-pex-with-homologies-to-endopeptidases-is-mutated-in-patients-with-x/)
- [Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study](https://scholariq.org/papers/range-of-genetic-mutations-associated-with-severe-non-syndromic-sporadic/)
- [Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment](https://scholariq.org/papers/polymorphisms-in-fkbp5-are-associated-with-increased-recurrence-of-depressive/)
- [An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita](https://scholariq.org/papers/an-unusual-member-of-the-nuclear-hormone-receptor-superfamily-responsible-for-x/)
- [Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia](https://scholariq.org/papers/haploinsufficiency-of-tbk1-causes-familial-als-and-fronto-temporal-dementia/)
- [Genome-wide, large-scale production of mutant mice by ENU mutagenesis](https://scholariq.org/papers/genome-wide-large-scale-production-of-mutant-mice-by-enu-mutagenesis/)
- [Genetic Spectrum and Clinical Correlates of Somatic Mutations in Aldosterone-Producing Adenoma](https://scholariq.org/papers/genetic-spectrum-and-clinical-correlates-of-somatic-mutations-in-aldosterone/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)

## Researcher university

- [TUM Klinikum](https://scholariq.org/institutions/tum-klinikum/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.