Tim M. Strom

53.7k citations

216 papers · 16.6k indexed · 6 hit papers · h-index 63

Nephrology top 0.05%
- Parathyroid Disorders and Treatments 23
Genetics top 0.1%
- Genomics and Rare Diseases 27
- Genetics and Neurodevelopmental Disorders 22
- Genomic variations and chromosomal abnormalities 15
Molecular Biology top 0.5%
- Mitochondrial Function and Pathology 20
- RNA modifications and cancer 12
Endocrinology, Diabetes and Metabolism top 0.5%
Rheumatology top 0.5%
Neurology
- Neurological diseases and metabolism 13
Clinical Biochemistry
- Metabolism and Genetic Disorders 12

Co-authors: Thomas Meitinger Bettina Lorenz‐Depiereux Anna Benet‐Pagès Michael J. Econs Kenneth E. White Monika Grabowski W. Evans Marcy C. Speer
Cited by: Nephrology Genetics Molecular Biology
Journals: European Journal of Human Genetics (16 papers)The American Journal of Human Genetics (16 papers)Clinical Genetics (7 papers)
Partner nations: Germany United States Austria

In The Last Decade

Tim M. Strom

213 papers receiving 16.2k citations

Hit Papers

6 papers align trajectories log scale

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.

2014 Nature Genetics
2005 The Lancet
2004 Nature
2000 Nature Genetics
1994 Nature
1994 Nature

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-authorship network

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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20 of 20 papers shown

#	Work
1	HNRNPA1 de novo Variant Associated with Early Childhood Onset, Rapidly Progressive Generalized Myopathy Journal of Neuromuscular Diseases ·Andreas Roos,Martin Häusler,Laxmikanth Kollipara,Ana Töpf,Corinna Preuße,Rolf Stucka,Kay Nolte,Tim M. Strom,Riccardo Berutti,田原信,Randi Koll,Hanns Lochmüller,신세운,René P. Zahedi,Joachim Weis,Jan Senderek	2024	2
2	Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders Human Molecular Genetics ·Theresa Brunet,Riccardo Berutti,Veronika Dill,Judith S. Hecker,Daniela Choukair,幸治竹田,Marcus Deschauer,Janine Diehl‐Schmid,Martin Krenn,Gertrud Eckstein,Elisabeth Graf,Thomas Gasser,Tim M. Strom,Julia Hoefele,Katharina S. Götze,Thomas Meitinger,Matias Wagner	2022	4
3	Novel pathogenic EIF2S3 missense variants causing clinically variable MEHMO syndrome with impaired eIF2γ translational function, and literature review Clinical Genetics ·Urania Kotzaeridou,Sara K. Young,Vanessa Suckow,دل آرا مردوخی,Matias Wagner,Inga Harting,Francis K. Kathimba,Tim M. Strom,Thomas Dever,Vera M. Kalscheuer	2020	10
4	Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder Clinical Genetics ·Nina B. Gold,Dong Li,Anna Chassevent,Frank J. Kaiser,Ilaria Parenti,Tim M. Strom,Feliciano J. Ramos,Beatriz Puisac,Juan Pié,Kirsty McWalter,María J. Guillen Sacoto,Hong Cui,Karin Weber,Constance Smith‐Hicks,Lance H. Rodan,Edward Blair,Elizabeth Bhoj	2020	10
5	A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy Annals of Clinical and Translational Neurology ·Melanie Brügger,Lee Becker,Theresa Brunet,Tim M. Strom,Thomas Meitinger,Eberhard Lurz,Ingo Borggraefe,Matias Wagner	2020	4
6	Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases EBioMedicine ·Miguel Gárriz Vera,Matias Wagner,Sarah L. Stenton,Tim M. Strom,Saskia B. Wortmann,Holger Prokisch,Thomas Meitinger,Konrad Oexle,Thomas Klopstock	2020	39
7	Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1 American Journal of Medical Genetics Part A ·Edith Said,Jessica X. Chong,Maja Hempel,Jonas Denecke,P Soler,Tim M. Strom,Deborah A. Nickerson,Christian Kubisch,Michael J. Bamshad,Davor Lessel	2017	8
8	Loss-of-function variants in HIVEP2 are a cause of intellectual disability European Journal of Human Genetics ·Siddharth Srivastava,Hartmut Engels,Ina Schanze,Kirsten Cremer,Thomas Wieland,Moritz Menzel,Max Schubach,Saskia Biskup,Martina Kreiß,Sabine Endele,Tim M. Strom,Dagmar Wieczorek,Martin Zenker,Siddharth Gupta,Julie S. Cohen,Alexander M. Zink,Sakkubai Naidu	2015	31
9	Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families PLoS ONE ·T Czerwinski,Saima Siddiqi,Margit Schraders,Jaap Oostrik,Humaira Ayub,Gerhard Wegen,Muhammad Ajmal,鲁烛,Tim M. Strom,Atika Mansoor,Kehkashan Mazhar,Syed Tahir Abbas Shah,Alamdar Hussain,Maleeha Azam,Hannie Kremer,Raheel Qamar	2014	53
10	An ENU Mutagenesis-Derived Mouse Model with a Dominant Jak1 Mutation Resembling Phenotypes of Systemic Autoimmune Disease American Journal Of Pathology ·Sibylle Sabrautzki,Fetiyana Luthfi Prihandini,Bettina Lorenz‐Depiereux,Julia Calzada‐Wack,Juan Antonio Aguilar‐Pimentel,Birgit Rathkolb,Thure Adler,Christian M. Cohrs,Wolfgang Hans,Susanne Diener,Helmut Fuchs,Valérie Gailus‐Durner,Dirk H. Busch,Heinz Höfler,Markus Ollert,Tim M. Strom,Eckhard Wolf,Frauke Neff,Martin Hrabě de Angelis	2013	19
11	Role of 5-hydroxymethylcytosine during postnatal retinal development Investigative Ophthalmology & Visual Science ·Stylianos Michalakis,金孔杰,Susanne Koch,Mirko Wagner,Lukas Windhager,Kerstin Nagel‐Wolfrum,Tim M. Strom,Ralf Zimmer,Thomas Carell,Martin Biel	2013	0
12	Targeted Next-Generation Sequencing for the Molecular Genetic Diagnostics of Cardiomyopathies Circulation Cardiovascular Genetics ·Benjamin Meder,Jan Haas,Andreas Keller,木村昌平,Steffen Just,Anne Borries,Valesca Boisguérin,Maren Scharfenberger‐Schmeer,Peer F. Stähler,Markus Beier,Dieter Weichenhan,Tim M. Strom,Arne Pfeufer,Bernhard Korn,Hugo A. Katus,(unknown)	2011	117
13	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 ·Rami Abou Jamra,S S Glick,Annick Raas‐Rothschild,Sebastian Eck,Elisabeth Graf,Rebecca Buchert,Guntram Borck,Arif B. Ekici,Felix F. Brockschmidt,Markus M. Nöthen,Arnold Münnich,Tim M. Strom,André Reis,Laurence Colleaux	2011	167
14	CpG-Methylation Regulates a Class of Epstein-Barr Virus Promoters PLoS Pathogens ·Jianting Ke,Markus Kalla,J EHeiserman,Christine Göbel,Ulrich Rothbauer,Sebastian Eck,Anna Benet‐Pagès,Tim M. Strom,Wolfgang Hammerschmidt	2010	91
15	Identification of Novel Retinal Degeneration Loci in Consanguineous Israeli and Palestinian Families With Retinal Disease Investigative Ophthalmology & Visual Science ·Dror Sharon,Tianming CHEN,Gabriela Soares Diniz Garcia,Tim M. Strom,S. Merin,Eyal Banin	2008	1
16	Polypeptide GalNAc-transferase T3 and Familial Tumoral Calcinosis Journal of Biological Chemistry ·Kentaro Kato,Charlotte Jeanneau,Mads A. Tarp,Anna Benet‐Pagès,Bettina Lorenz‐Depiereux,Eric Bennett,Ulla Mandel,Tim M. Strom,Henrik Clausen	2006	342
17	An autosomal recessive hypophosphatemic disorder caused by homozygous mutations in dentin matrix protein 1 (DMP1). Journal of Bone and Mineral Research ·Murat Bastepe,Bettina Lorenz‐Depiereux,Prof. S.P. Bhuyarkar,Michella Ghassibe‐Sabbagh,Janine Wagenstaller,Spenser Davenport Simrill,Klaus Badenhoop,Roger S. Rittmaster,Mariam Kiran,J. Olivares,Feliciano J. Ramos,Miikka Vikkula,Tim M. Strom,Harald Jüeppner	2006	0
18	An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia Human Molecular Genetics ·Anna Benet‐Pagès,Peter Orlik,Tim M. Strom,Bettina Lorenz‐Depiereux	2004	373
19	The Autosomal Dominant Hypophosphatemic Rickets (ADHR) Gene Is a Secreted Polypeptide Overexpressed by Tumors that Cause Phosphate Wasting The Journal of Clinical Endocrinology & Metabolism ·Kenneth E. White,Kenneth B. Jonsson,Gwénaëlle Carn,Geeta Hampson,Tim D. Spector,Michael Mannstadt,Bettina Lorenz‐Depiereux,Akimitsu Miyauchi,In Myung Yang,Östen Ljunggren,Thomas Meitinger,Tim M. Strom,Harald Jüppner,Michael J. Econs	2001	231
20	Mechanisms of action of atrial natriuretic factor: clinical consequences. PubMed ·R. Gerzer,J. Weil,Tim M. Strom,In kyong Cho	1986	14

About Tim M. Strom

Tim M. Strom is a scholar working on Nephrology, Genetics and Neurology, having authored 216 papers that have together received 16.6k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (27 papers), Parathyroid Disorders and Treatments (23 papers), Genetics and Neurodevelopmental Disorders (22 papers), Mitochondrial Function and Pathology (20 papers), Genomic variations and chromosomal abnormalities (15 papers), Neurological diseases and metabolism (13 papers), RNA modifications and cancer (12 papers) and Metabolism and Genetic Disorders (12 papers). The work is most often cited by research in Nephrology (3.5k citations), Genetics (6.0k citations) and Molecular Biology (8.0k citations). Tim M. Strom has collaborated with scholars based in Germany, United States and Austria. Frequent 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. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Clinical Genetics, Human Molecular Genetics and Nature Genetics.

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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