Martin Zenker

Also affiliated with University Hospital Magdeburg, Otto-von-Guericke-Universität Magdeburg

Biochemistry, Genetics and Molecular BiologyImmunology and MicrobiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 16 papers. Top paper: “Clinical overview on RASopathies”.

Clinical overview on RASopathies

American Journal of Medical Genetics Part C: Seminars in Medical Genetics(2022)10.1002/ajmg.c.32015

N/A

0.670DataRank · unranked

86 citations

Martin Zenker

Impact of MEK Inhibition on Childhood RASopathy-Associated Hypertrophic Cardiomyopathy

JACC Basic to Translational Science(2024)10.1016/j.jacbts.2024.10.002

N/A

0.625DataRank · unranked

22 citations

Martin Zenker, Olga Boleti, Gabrielle Norrish, Mark W. Russell, Joshua K. Meisner +37 more

Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome

Journal of the American Society of Nephrology(2021)10.1681/asn.2020040490

N/A

0.505DataRank · unranked

28 citations

Slim Mzoughi, Ronen Schneider, Susanne J. Kühl, Denny Schanze, Verena Klämbt +38 more

Unusual phenotypes in patients with a pathogenic germline variant in DICER1

Familial Cancer(2021)10.1007/s10689-021-00271-z

N/A

0.373DataRank · unranked

11 citations

Miriam Elbracht, Julia Carlens, Peter Deutz, Felix Zeppernick, Lisa Lassay +10 more

Responsiveness of sphingosine phosphate lyase insufficiency syndrome to vitamin B6 cofactor supplementation

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12238

N/A

0DataRank · unranked

34 citations

Isaac D Liu, Jeffrey B. Hodgin, Peter I. Benke, Jeremy Selva, Federico Torta +22 more

MRI Spectrum of Brain Involvement in Sphingosine-1-Phosphate Lyase Insufficiency Syndrome

American Journal of Neuroradiology(2020)10.3174/ajnr.a6746

N/A

0DataRank · unranked

25 citations

K. Nicole Weaver, Khalid Alhasan, Evren Gümüş, Bonnie Sullivan, Martin Zenker +3 more

NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

Nature Communications(2020)10.1038/s41467-020-18327-6

N/A

0DataRank · unranked

101 citations

Yu Kigoshi-Tansho, Roger B. Sher, Gianina Ravenscroft, Jennifer E. Stauffer, Rajesh Kumar +23 more

The seventh international RASopathies symposium: Pathways to a cure—expanding knowledge, enhancing research, and therapeutic discovery

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62716

N/A

0DataRank · unranked

16 citations

Amy E. Roberts, Lisa Schill, Lisa Schoyer, Beth Stronach, Grégor Andelfinger +37 more

Infantile epileptic spasms syndrome in children with cardiofaciocutanous syndrome: Clinical presentation and associations with genotype

American Journal of Medical Genetics Part C Seminars in Medical Genetics(2022)10.1002/ajmg.c.32022

N/A

0DataRank · unranked

10 citations

Dante J. Rogers, Samuel J. Kroening, Abigail L Zatkalik, Ashley E. Whitmarsh, Amy E. Roberts +10 more

The 8th International RASopathies Symposium: Expanding research and care practice through global collaboration and advocacy

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63477

N/A

0DataRank · unranked

7 citations

Anton M. Bennett, Lisa Schoyer, Beth Stronach, April Anschutz, Sarah C. Borrie +39 more

Epilepsy in cardiofaciocutaneous syndrome: Clinical burden and response to anti‐seizure medication

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63428

N/A

0DataRank · unranked

4 citations

Josue E. Collazo‐Lopez, Dante J. Rogers, Ryan Shanley, Abigail L Zatkalik, Ashley E. Whitmarsh +4 more

GGC expansion in ZFHX3 causes SCA4 and impairs autophagy

medRxiv(2023)10.1101/2023.10.26.23297560

N/A

0DataRank · unranked

3 citations

Caspar Groß, Elena Buena Atienza, Sharan Paul, Mandi Gandelman, Tobias B. Haack +25 more

Neurologic and neurodevelopmental complications in cardiofaciocutaneous syndrome are associated with genotype: A multinational cohort study

Genetics in Medicine(2022)10.1016/j.gim.2022.04.004

N/A

0DataRank · unranked

41 citations

Daniel Kenney‐Jung, Ryan Shanley, Abigail L Zatkalik, Ashley E. Whitmarsh, Samuel J. Kroening +3 more

Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.018

N/A

0DataRank · unranked

93 citations

Luca Pannone, Francesca Pantaleoni, Gianfranco Bocchinfuso, Francesca Clementina Radio, Serena Cecchetti +45 more

KrasP34R and KrasT58I mutations induce distinct RASopathy phenotypes in mice

JCI Insight(2020)10.1172/jci.insight.140495

N/A

0DataRank · unranked

32 citations

Pedro A. Pérez–Mancera, Tannie Q. Huang, Jangkyung Kim, Joaquím Grego‐Bessa, Maria del pilar Alzamora +15 more

Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome

Wellcome Open Research(2020)10.12688/wellcomeopenres.15465.2

N/A

0DataRank · unranked

11 citations

Senthil Senniappan, Thomas W. Laver, Richard Caswell, Martin Zenker, Klaus Mohnike +17 more