Melissa Walker

Also affiliated with Alfred Health

Biochemistry, 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 1%percentile

6.0Author 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations

Nucleic Acids Research(2020)10.1093/nar/gkaa1011

Top 3%

6.0DataRank

Top 3%2013 citations

Rohit Sharma, Rahul Gupta, Tslil Ast, Connie Chan, Timothy Durham +27 more

Papers

Driven by 21 papers — median percentile 97. Top paper: “MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations”.

MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations

Nucleic Acids Research(2020)10.1093/nar/gkaa1011

Top 3%

6.0DataRank

Top 3%2013 citations

Rohit Sharma, Rahul Gupta, Tslil Ast, Connie Chan, Timothy Durham +27 more

Caenorhabditis elegans methionine/S-adenosylmethionine cycle activity is sensed and adjusted by a nuclear hormone receptor

eLife(2020)10.7554/elife.60259

N/A

1.7DataRank · unranked

73 citations

Melissa Walker, Olga Ponomarova, Hefei Zhang, Xuhang Li, Gregory Minevich +2 more

De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment

Human Molecular Genetics(2020)10.1093/hmg/ddaa081

N/A

1.1DataRank · unranked

41 citations

Lauren C. Briere, Oguz Kanca, Paul C. Marcogliese, Melissa Walker, Frances A. High +13 more

SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia

Brain(2023)10.1093/brain/awac460

N/A

0.992DataRank · unranked

35 citations

Hagar Mor Shaked, Kenneth Gable, Sita D. Gupta, Xueyang Pan, Niranjanakumari Somashekarappa +93 more

A description of novel variants and review of phenotypic spectrum in UBA5-related early epileptic encephalopathy

Molecular Case Studies(2021)10.1101/mcs.a005827

N/A

0DataRank · unranked

30 citations

Melissa Walker, Frances A. High, Cynthia A. Cooper, Cassandra A. Rogers, Christine J. Callahan +14 more

The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.011

N/A

0DataRank · unranked

27 citations

Gabrielle Lemire, Lauren C. Briere, Fang Liu, Marja W. Wessels, Xueqi Wang +13 more

Bacterial diet modulates tamoxifen-induced death via host fatty acid metabolism

Nature Communications(2022)10.1038/s41467-022-33299-5

N/A

0DataRank · unranked

25 citations

Aurian P. García-González, Andre F.C. Vieira, Melissa Walker, Megan E. Honeywell, Hailey Doyle +8 more

A homozygous splice variant in ATP5PO, disrupts mitochondrial complex V function and causes Leigh syndrome in two unrelated families

Journal of Inherited Metabolic Disease(2022)10.1002/jimd.12526

N/A

0DataRank · unranked

17 citations

Gaëlle Friocourt, Naïg Guéguen, Marisa W. Friederich, Gérald Le Gac, Volkan Okur +34 more

Perspectives of Rare Disease Experts on Newborn Genome Sequencing

JAMA Network Open(2023)10.1001/jamanetworkopen.2023.12231

N/A

0DataRank · unranked

51 citations

Sophia Adelson, Nidhi Shah, Shardae Williams, Sarah L. Bick, Emilie S. Zoltick +17 more

A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster

Genetics(2023)10.1093/genetics/iyad110

N/A

0DataRank · unranked

12 citations

Lauren C. Briere, Kristy L. Jay, Jonathan C. Andrews, Melissa Walker, Lance H. Rodan +6 more

Endocrine features of primary mitochondrial diseases

Current Opinion in Endocrinology Diabetes and Obesity(2023)10.1097/med.0000000000000848

N/A

0DataRank · unranked

10 citations

Nina B. Gold, Melissa Walker, Lindsay Romo

High-dimensional immunophenotyping reveals immune cell aberrations in patients with undiagnosed inflammatory and autoimmune diseases

Journal of Clinical Investigation(2023)10.1172/jci169619

N/A

0DataRank · unranked

3 citations

Takanori Sasaki, Joshua Keegan, Jennifer P. Nguyen, Alec Griffith, Alice Horisberger +21 more

A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster

medRxiv(2023)10.1101/2023.01.31.23285113

N/A

0DataRank · unranked

0 citations

Lauren C. Briere, Kristy Jay, Jonathan C. Andrews, Melissa Walker, Lance H. Rodan +6 more

The Effect of Disease on the Developing Nervous System: Challenges and Opportunities, a Foreward

Pediatric Neurology(2023)10.1016/j.pediatrneurol.2023.10.013

N/A

0DataRank · unranked

0 citations

Melissa Walker, Grace Gombolay

Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2322582121

N/A

0DataRank · unranked

6 citations

Oguz Kanca, Rishi V. Shridharan, Paul C. Marcogliese, Benjamin Steger, Marie Morimoto +92 more

T cell activation contributes to purifying selection against the MELAS‐associated m.3243A>G pathogenic variant in blood

Journal of Inherited Metabolic Disease(2024)10.1002/jimd.12726

N/A

0DataRank · unranked

6 citations

Shuqiang Li, Kenneth J. Livak, Amel Karaa, Catherine J. Wu, Vamsi K. Mootha +1 more

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174

N/A

0DataRank · unranked

4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more

Advancing precision care in pregnancy through a treatable fetal findings list

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.011

N/A

0DataRank · unranked

10 citations

Michael Duyzend, Sophia Adelson, Julie Yeo, Mark D. Fleming, Rebecca Ganetzky +12 more

Purifying Selection against Pathogenic Mitochondrial DNA in Human T Cells

New England Journal of Medicine(2020)10.1056/nejmoa2001265

N/A

0DataRank · unranked

100 citations

Caleb A. Lareau, Leif S. Ludwig, Amel Karaa, Vijay G. Sankaran, Aviv Regev +2 more

Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

Genetics in Medicine(2020)10.1038/s41436-020-00984-z

N/A

0DataRank · unranked

42 citations

Cecilia Esteves, Anna Bican, Rebecca C. Spillmann, Heidi Cope, Allyn McConkie‐Rosell +89 more

Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity

Journal of Clinical Investigation(2021)10.1172/jci136055

N/A

0DataRank · unranked

202 citations

Bryn Reinstadler, Kristin Engelstad, Owen S. Skinner, Erin Stackowitz, Ronald G. Haller +12 more

Melissa Walker

Indexed papers

Top data-sharing exemplar

Papers