Tim M. Strom

2.7k citations

15 papers · 2.1k · 1 hit paper · h-index 15

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism

Papers in

Clinical Biochemistry 6
- Metabolism and Genetic Disorders 6
Molecular Biology 12
- Mitochondrial Function and Pathology 7
- ATP Synthase and ATPases Research 3
- RNA modifications and cancer 2

Co-authors: Tobias B. Haack (3 shared papers)Thomas Meitinger (3 shared papers)Elisabeth Graf (2 shared papers)Thomas Wieland (2 shared papers)Holger Prokisch (2 shared papers)Sylvia Boesch (1 shared paper)Bader Alhaddad (1 shared paper)Werner H Poewe (1 shared paper)
Journals: The American Journal of Human Genetics (14 papers)Genetics in Medicine (1 paper)
Partner nations: Germany Austria United Kingdom

In The Last Decade

Tim M. Strom

15 papers receiving 2.1k citations

Tim M. Strom's Hit Papers

align trajectories log scale

A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease 2011 · 722 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2011 The American Journal of Human Genetics

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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15 of 15 papers shown

#	Work
1	A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease The American Journal of Human Genetics ·Alexander A. Zimprich, Anna Benet‐Pagès, Walter Struhal, Elisabeth Graf, Sebastian H. Eck, Marc N. Offman, Dietrich Haubenberger, Sabine Spielberger Hit paper breakdown →	2011	722
2	Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation The American Journal of Human Genetics ·Sabrina Dusi, Lorella Valletta, Tobias B. Haack, Yugo Tsuchiya, Paola Venco, Sebastiano Pasqualato, Paola Goffrini, Marco Tigano	2013	177
3	Mutations in FBXL4, Encoding a Mitochondrial Protein, Cause Early-Onset Mitochondrial Encephalomyopathy The American Journal of Human Genetics ·Xiaowu Gai, Daniele Ghezzi, Mark A. Johnson, Caroline Biagosch, Hanan E. Shamseldin, Tobias B. Haack, Aurelio Reyes, Mai Tsukikawa	2013	146
4	Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy The American Journal of Human Genetics ·Robert Kopajtich, Thomas J. J. Nicholls, Joanna Rorbach, Metodi Dimitrov Metodiev, Peter Freisinger, Hanna Mandel, Arnaud Vincent Vanlander, Daniele Ghezzi	2014	134
5	Haploinsufficiency of KMT2B, Encoding the Lysine-Specific Histone Methyltransferase 2B, Results in Early-Onset Generalized Dystonia The American Journal of Human Genetics ·Michael Zech, Sylvia Boesch, Esther M. Maier, Ingo Borggraefe, Katharina Vill, Franco A. Laccone, Veronika Pilshofer, Andrés Ceballos-Baumann	2016	134
6	CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder The American Journal of Human Genetics ·Saskia B. Wortmann, Szymon Ziętkiewicz, Maria Kousi, Radek Szklarczyk, Tobias B. Haack, Søren W. Gersting, Ania Carolina Muntau, Aleksandar Raković	2015	109
7	Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island The American Journal of Human Genetics ·Alice Hadchouel, Thomas Wieland, Matthias Griese, Enrico Baruffini, Bettina Lorenz‐Depiereux, Laurent Enaud, Elisabeth Graf, Jean-Christophe Dubus	2015	103
8	Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy The American Journal of Human Genetics ·Tobias B. Haack, Christian Staufner, Marlies Köpke, Beate Katharina Straub, Stefan Kölker, Christian T. Thiel, Peter Freisinger, Ivo Barić	2015	102
9	Absence of BiP Co-chaperone DNAJC3 Causes Diabetes Mellitus and Multisystemic Neurodegeneration The American Journal of Human Genetics ·Matthis Synofzik, Tobias B. Haack, Robert Kopajtich, Matteo Gorza, Doron Rapaport, Markus Greiner, Caroline Schönfeld, Clemens Freiberg	2014	94
10	DHTKD1 Mutations Cause 2-Aminoadipic and 2-Oxoadipic Aciduria The American Journal of Human Genetics ·Katharina Danhauser, Sven W. Sauer, Tobias B. Haack, Thomas Wieland, Christian Staufner, Elisabeth Graf, Johannes Zschocke, Tim M. Strom	2012	92
11	Bi-allelic Truncating Mutations in TANGO2 Cause Infancy-Onset Recurrent Metabolic Crises with Encephalocardiomyopathy The American Journal of Human Genetics ·Laura Sophie Kremer, Felix Distelmaier, Bader Alhaddad, Maja Hempel, Arcangela Iuso, Clemens Küpper, Chris Mühlhausen, Réka Kovács-Nagy	2016	85
12	Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile Hepatopathy The American Journal of Human Genetics ·Robert Kopajtich, Kei Murayama, Andreas Janecke, Tobias B. Haack, Maximilian Breuer, Alex S. Knisely, Inga Harting, Toya Ohashi	2016	71
13	Mutations in APOPT1, Encoding a Mitochondrial Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency The American Journal of Human Genetics ·Laura Melchionda, Tobias B. Haack, Steven A. Hardy, Truus E. M. Abbink, Erika Fernández‐Vizarra, Eleonora Lamantea, Silvia Marchet, Lucia Ovidia Morandi	2014	59
14	Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2 The American Journal of Human Genetics ·Hannah Kennedy, Tobias B. Haack, Verity L. Hartill, Lavinija Mataković, E. R. Baumgartner, Howard C. Potter, Richard J Mackay, Charlotte L. Alston	2016	53
15	Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy Genetics in Medicine ·Joohyun Park, Arianna Tucci, Valentina Cipriani, German Demidov, Clarissa Rocca, Jan Senderek, Michaela Butryn, Ana Velić	2022	15

About Tim M. Strom

Tim M. Strom is a scholar working on Clinical Biochemistry, Molecular Biology, Neurology, Genetics and Cellular and Molecular Neuroscience, having authored 15 papers that have together received 2.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (6 papers), ATP Synthase and ATPases Research (3 papers), RNA modifications and cancer (2 papers), Genetic Neurodegenerative Diseases (2 papers), Neurological diseases and metabolism (2 papers), Genomics and Rare Diseases (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Clinical Biochemistry (341 citations), Neurology (344 citations), Neurology (558 citations), Cell Biology (345 citations) and Cellular and Molecular Neuroscience (306 citations). Tim M. Strom has collaborated with scholars based in Germany, Austria and United Kingdom. Frequent co-authors include Tobias B. Haack, Thomas Meitinger, Elisabeth Graf, Thomas Wieland, Holger Prokisch, Sylvia Boesch, Bader Alhaddad, Werner H Poewe, Bernhard A. Haslinger and Michael Zech. Their work appears in journals such as The American Journal of Human Genetics and Genetics in Medicine.

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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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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