Donna M. Martin

ORCID: 0000-0002-8070-2007

MedicineBiochemistry, Genetics and Molecular Biology

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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 18 papers. Top paper: “A road map for the treatment of pediatric diffuse midline glioma”.

A road map for the treatment of pediatric diffuse midline glioma

Cancer Cell(2023)10.1016/j.ccell.2023.11.002

N/A

0.653DataRank · unranked

24 citations

Wajd N. Al‐Holou, Marta M. Alonso, Jamie N. Anastas, Pratiti Bandopadhayay, Tara Barron +70 more

Erratum to “The influence of 5-HTTLPR transporter genotype on amygdala-subgenual anterior cingulate cortex connectivity in autism spectrum disorder” [Dev. Cognit. Neurosci. 24 April (2017) 12–20]

Developmental Cognitive Neuroscience(2020)10.1016/j.dcn.2020.100844

N/A

0DataRank · unranked

0 citations

Jillian Lee Wiggins, Whitney I. Mattson, Donna M. Martin, Catherine Lord, Christopher S. Monk +1 more

CHARGE SYNDROME

University of Groningen research database (University of Groningen / Centre for Information Technology)(2020)10.1002/9781119432692.ch11

N/A

0DataRank · unranked

0 citations

Christine A. Oley, Conny M.A. van Ravenswaaij‐Arts, Donna M. Martin

GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function

Molecular Therapy — Methods & Clinical Development(2021)10.1016/j.omtm.2021.09.009

N/A

0DataRank · unranked

47 citations

Xiaobo Ma, Jennifer Skidmore, Jelka Cimerman, Diane M. Prieskorn, Lisa A. Beyer +5 more

Chromatin remodeler CHD7 is critical for cochlear morphogenesis and neurosensory patterning

Developmental Biology(2021)10.1016/j.ydbio.2021.05.009

N/A

0DataRank · unranked

10 citations

Jennifer Skidmore, Kristina Ritter, Jingxia Gao, Jelka Cimerman, Lisa A. Beyer +4 more

Single-cell lineage trajectories and chromatin regulators that initialize antiviral CD8 T cell ontogeny

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.11.456014

N/A

0DataRank · unranked

2 citations

Runqiang Chen, Shanel Tsuda, Dapeng Wang, Megan A. Frederick, Jihye Kim +11 more

GIGYF1 disruption associates with autism and impaired IGF-1R signaling

Journal of Clinical Investigation(2022)10.1172/jci159806

N/A

0DataRank · unranked

32 citations

Bin Yu, Senwei Tan, Jieqiong Tan, Xiangbin Jia, Qiumeng Zhang +29 more

Challenges of variant reinterpretation: Opinions of stakeholders and need for guidelines

Genetics in Medicine(2022)10.1016/j.gim.2022.06.002

N/A

0DataRank · unranked

29 citations

Paul S. Appelbaum, Karolynn Siegel, Julia Wynn, Akilan M. Saami, Elly Brokamp +5 more

Epigenetic mechanisms of inner ear development

Hearing Research(2022)10.1016/j.heares.2022.108440

N/A

0DataRank · unranked

9 citations

Kristina Ritter, Donna M. Martin, Vinodh Balendran

Loss of the chromatin remodeler CHD7 impacts glial cells and myelination in the mouse cochlear spiral ganglion

Hearing Research(2022)10.1016/j.heares.2022.108633

N/A

0DataRank · unranked

5 citations

Sloane M. Lynch, Ashley M. Gorris, Lisa A. Beyer, Lisa Kabara, David F. Dolan +3 more

Chromatin remodeler Chd7 regulates photoreceptor development and outer segment length

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.05.30.494019

N/A

0DataRank · unranked

1 citations

Jessica D. Bills, Zun Yi Lim, Jennifer Skidmore, Donna M. Martin, Ann C. Morris +1 more

Regulation of cellular LDL uptake by PROX1 and CHD7

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.20.507601

N/A

0DataRank · unranked

1 citations

Matthew L. Holding, Taslima Khan, Vi T. Tang, Jennifer Skidmore, Donna M. Martin +3 more

Practical considerations for reinterpretation of individual genetic variants

Genetics in Medicine(2023)10.1016/j.gim.2023.100801

N/A

0DataRank · unranked

24 citations

Sara M. Berger, Elly Brokamp, H. Shelton Brown, Wylie Burke, Ellen Wright Clayton +14 more

CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct

Human Genetics(2023)10.1007/s00439-023-02581-x

N/A

0DataRank · unranked

13 citations

Cristina Fenollar‐Ferrer, Hyun Jae Lee, Parna Chattaraj, Iván A. López, Kyungreem Han +7 more

CHD7 and SOX2 act in a common gene regulatory network during mammalian semicircular canal and cochlear development

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2311720121

N/A

0DataRank · unranked

13 citations

Jennifer Skidmore, Jelka Cimerman, Kristina Ritter, Jingyun Qiu, Lindsey M. Q. Wilson +4 more

A novel cardiomyopathy phenotype linked to a CHD7 missense variant

Scientific Reports(2025)10.1038/s41598-025-00606-1

N/A

0DataRank · unranked

2 citations

Chih‐Wei Hsu, Karim Bouazoune, Christina E Espindola, Madeline Hannah McLaughlin Armond, Cristian Coarfa +5 more

CHD7 promotes neural progenitor differentiation in embryonic stem cells via altered chromatin accessibility and nascent gene expression

Scientific Reports(2020)10.1038/s41598-020-74537-4

N/A

0DataRank · unranked

37 citations

D. Ford Hannum, Yiwen Zhai, Sophie F. Hill, Ricardo D’Oliveira Albanus, Wenjia Lou +9 more

A clinical and genotype-phenotype analysis of MACF1 variants

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.010

N/A

0DataRank · unranked

1 citations

Rachel Schot, Kimberly A. Aldinger, David B. Everman, Camerun Washington, Julie R. Jones +85 more