David Dimmock

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 4%percentile

0.604Author 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.

The evolution of the mitochondrial disease diagnostic odyssey

Orphanet Journal of Rare Diseases(2023)10.1186/s13023-023-02754-x

Top 33%

0.604DataRank

Top 33%19 citations

Amel Karaa, Hung Viet Pham, Philip E. Yeske, Jeffrey P. Krischer, Yi Xiao +10 more

Papers

Driven by 20 papers — median percentile 67. Top paper: “Wastewater sequencing reveals early cryptic SARS-CoV-2 variant transmission”.

Wastewater sequencing reveals early cryptic SARS-CoV-2 variant transmission

Nature(2022)10.1038/s41586-022-05049-6

N/A

0.939DataRank · unranked

523 citations

Joshua I. Levy, Peter De Hoff, Greg Humphrey, Amanda Birmingham, Kristen Jepsen +95 more

At the intersection of precision medicine and population health: an implementation-effectiveness study of family health history based systematic risk assessment in primary care

BMC Health Services Research(2020)10.1186/s12913-020-05868-1

N/A

0.924DataRank · unranked

31 citations

R. Ryanne Wu, Rachel A. Myers, Joan Neuner, Catherine A. McCarty, Irina V. Haller +7 more

The evolution of the mitochondrial disease diagnostic odyssey

Orphanet Journal of Rare Diseases(2023)10.1186/s13023-023-02754-x

Top 33%

0.604DataRank

Top 33%19 citations

Amel Karaa, Hung Viet Pham, Philip E. Yeske, Jeffrey P. Krischer, Yi Xiao +10 more

Implementation-effectiveness trial of systematic family health history based risk assessment and impact on clinical disease prevention and surveillance activities

BMC Health Services Research(2022)10.1186/s12913-022-08879-2

N/A

0.546DataRank · unranked

13 citations

Rachel A. Myers, Joan Neuner, Catherine A. McCarty, Irina V. Haller, Melissa L. Harry +7 more

Abnormal SCID Newborn Screening and Spontaneous Recovery Associated with a Novel Haploinsufficiency IKZF1 Mutation

Journal of Clinical Immunology(2021)10.1007/s10875-021-01035-1

N/A

0.505DataRank · unranked

8 citations

Nicholas J. Gloude, David Dimmock, Mari Tokita, Meredith S. Wright, Sergio D. Rosenzweig +2 more

ECHS1 disease in two unrelated families of Samoan descent: Common variant ‐ rare disorder

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61936

N/A

0.500DataRank · unranked

27 citations

Shaya S. Eftekharian, Sacha Ferdinandusse, Sha Tang, Take Naseri, Muagututi‘a Sefuiva Reupena +12 more

Insights into the perinatal phenotype of Kabuki syndrome in infants identified by genome‐wide sequencing

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63097

N/A

0.208DataRank · unranked

3 citations

Monia Hammer, Mari Tokita, Priyanka Patel, Marilyn C. Jones, Austin Larson +17 more

Response to Grosse et al.

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.004

N/A

0.104DataRank · unranked

1 citations

Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Serge Batalov, Wendy Benson +46 more

Variant STAT4 and Response to Ruxolitinib in an Autoinflammatory Syndrome

New England Journal of Medicine(2023)10.1056/nejmoa2202318

N/A

0DataRank · unranked

79 citations

Sarah A. Blackstone, Gwendolyn Clay, Rachael L. Philips, Brynja Matthiasardottir, Michele Nehrebecky +36 more

Genomic sequencing has a high diagnostic yield in children with congenital anomalies of the heart and urinary system

Frontiers in Pediatrics(2023)10.3389/fped.2023.1157630

N/A

0DataRank · unranked

11 citations

Elliot A. Perens, Nicole G. Coufal, Erica Sanford Kobayashi, Stephen F. Kingsmore, David Dimmock +1 more

The Genomic landscape of short tandem repeats across multiple ancestries

PLoS ONE(2023)10.1371/journal.pone.0279430

N/A

0DataRank · unranked

8 citations

Serge Batalov, Yan Ding, Erica Sanford Kobayashi, Stephen F. Kingsmore, David Dimmock +3 more

An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.10.003

N/A

0DataRank · unranked

191 citations

Michelle M. Clark, Mary Gaughran, Julie A. Cakici, Sara Caylor, Christina Clarke +62 more

Clinical characterization of Collagen XII‐related disease caused by biallelic COL12A1 variants

Annals of Clinical and Translational Neurology(2025)10.1002/acn3.52225

N/A

0DataRank · unranked

3 citations

Dimah Saade, Pinki Munot, Chamindra G. Laverty, Hailey Pinz, Yaqun Zou +24 more

A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.10.004

N/A

0DataRank · unranked

99 citations

David Dimmock, Sara Caylor, Mary Gaughran, Christina Clarke, Cynthia Triplett +4 more

Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12232

N/A

0DataRank · unranked

62 citations

Abdallah F. Elias, Alice Küster, Lucia Laugwitz, Austin Larson, Aaron P. Landry +16 more

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

npj Genomic Medicine(2021)10.1038/s41525-021-00192-x

N/A

0DataRank · unranked

76 citations

Shareef Nahas, Shimul Chowdhury, Serge Batalov, Michelle M. Clark, Sara Caylor +8 more

Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases

Genetics in Medicine(2021)10.1038/s41436-021-01200-2

N/A

0DataRank · unranked

26 citations

Marvid S. Duarte Moreno, Jean‐François Benoist, Manfred Boehm, E. Bourrat, Aline Cano +28 more

Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

npj Genomic Medicine(2021)10.1038/s41525-021-00206-8

N/A

0DataRank · unranked

6 citations

Shareef Nahas, Shimul Chowdhury, Serge Batalov, Michelle M. Clark, Sara Caylor +8 more

Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

npj Genomic Medicine(2021)10.1038/s41525-021-00205-9

N/A

0DataRank · unranked

5 citations

Shareef Nahas, Shimul Chowdhury, Serge Batalov, Michelle M. Clark, Sara Caylor +8 more

A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.003

N/A

0DataRank · unranked

171 citations

Laurie D. Smith, Chris M. Kunard, Matthew Bainbridge, Sergey Batalov, Wendy Benson +46 more

David Dimmock

Indexed papers

Top data-sharing exemplar

Papers