David Dimmock

13.6k total citations · 2 hit papers
116 papers, 3.9k citations indexed

About

David Dimmock is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, David Dimmock has authored 116 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 53 papers in Genetics and 34 papers in Clinical Biochemistry. Recurrent topics in David Dimmock's work include Genomics and Rare Diseases (37 papers), Metabolism and Genetic Disorders (33 papers) and Mitochondrial Function and Pathology (27 papers). David Dimmock is often cited by papers focused on Genomics and Rare Diseases (37 papers), Metabolism and Genetic Disorders (33 papers) and Mitochondrial Function and Pathology (27 papers). David Dimmock collaborates with scholars based in United States, Canada and United Kingdom. David Dimmock's co-authors include Stephen F. Kingsmore, Michelle M. Clark, David Bick, Lauge Farnaes, Daniel Helbling, Susan M. White, Tiong Yang Tan, Zornitza Stark, Lee‐Jun C. Wong and Shimul Chowdhury and has published in prestigious journals such as Nature, New England Journal of Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

David Dimmock

114 papers receiving 3.9k citations

Hit Papers

align trajectories

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.

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases

2018 340 citations Lauge Farnaes, David Dimmock et al. npj Genomic Medicine profile →
Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization

2018 280 citations Lauge Farnaes, Shimul Chowdhury et al. npj Genomic Medicine profile →

Peers

Countries citing papers authored by David Dimmock

Since Specialization

Citations

This map shows the geographic impact of David Dimmock'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 David Dimmock with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Dimmock more than expected).

Fields of papers citing papers by David Dimmock

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David Dimmock. 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 David Dimmock. The network helps show where David Dimmock may publish in the future.

Co-authorship network of co-authors of David Dimmock

This figure shows the co-authorship network connecting the top 25 collaborators of David Dimmock. A scholar is included among the top collaborators of David Dimmock based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with David Dimmock. David Dimmock is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Palliative Care Outcomes for Critically ill Children After Rapid Whole Genome Sequencing 2024 ·Journal of Intensive Care Medicine ·(unknown), (unknown), (unknown), (unknown), (unknown), David Dimmock, Stephen F. Kingsmore, Nicole G. Coufal	0
2	Parent and patient knowledge and attitudes about cancer predisposition syndrome genetic testing in pediatric oncology: Understanding sociodemographic and parent–child differences 2024 ·Cancer Reports ·(unknown), Diane Masser‐Frye, (unknown), (unknown), (unknown), (unknown), (unknown), David Dimmock, Vanessa L. Malcarne, Dennis John Kuo	1
3	The Genomic landscape of short tandem repeats across multiple ancestries 2023 ·PLoS ONE ·Prashanth Vijayaraghavan, Serge Batalov, Yan Ding, Erica Sanford Kobayashi, Stephen F. Kingsmore, David Dimmock, Charlotte A. Hobbs, Matthew Bainbridge	2
4	Breaking Barriers to Rapid Whole Genome Sequencing in Pediatrics: Michigan’s Project Baby Deer 2023 ·Children ·Caleb Bupp, Elizabeth G. Ames, (unknown), Sara Caylor, David Dimmock, (unknown), Padmani Karna, (unknown), Cristian Meghea, Vinod K. Misra, Danielle Nolan, John J. O’Shea, (unknown), Linda S. Franck, (unknown)	17
5	The evolution of the mitochondrial disease diagnostic odyssey 2023 ·Orphanet Journal of Rare Diseases ·John L.P. Thompson, Amel Karaa, Hung Viet Pham, Philip E. Yeske, Jeffrey P. Krischer, Yi Xiao, (unknown), (unknown), David Dimmock, (unknown), (unknown), Kristin Engelstad, Richard Buchsbaum, Xiomara Q. Rosales, Michio Hirano	6
6	Novel Approach to Improve the Identification of the Bleeding Phenotype in Noonan Syndrome and Related RASopathies 2023 ·The Journal of Pediatrics ·(unknown), Jerica Lenberg, Dzung Le, David Dimmock, Courtney D. Thornburg, Benjamin Briggs	2
7	Rapid genome sequencing identifies novel variants in complement factor I 2022 ·Molecular Case Studies ·(unknown), (unknown), (unknown), (unknown), (unknown), Edsel M. Abud, Yuzhou Zhang, Richard J. Smith, (unknown), (unknown), Hal M. Hoffman, (unknown), David Dimmock, Nicole G. Coufal	2
8	Healthcare Professionals’ Attitudes toward Rapid Whole Genome Sequencing in Pediatric Acute Care 2022 ·Children ·Linda S. Franck, (unknown), Caleb Bupp, (unknown), Thomas J. Hoffmann, (unknown), (unknown), David Dimmock	8
9	Immune Responses and Immunosuppressive Strategies for Adeno-Associated Virus-Based Gene Therapy for Treatment of Central Nervous System Disorders: Current Knowledge and Approaches 2022 ·Human Gene Therapy ·Suyash Prasad, David Dimmock, Benjamin Greenberg, Jagdeep S. Walia, Chanchal Sadhu, (unknown), Gerald S. Lipshutz	36
10	Hemimegalencephaly and intractable seizures associated with the NPRL3 gene variant in a newborn: A case report 2021 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Jason Carmichael, Kiely N. James, Katarzyna A. Ellsworth, David Dimmock, (unknown)	12
11	Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease 2020 ·npj Genomic Medicine ·Christian R. Marshall, Shimul Chowdhury, Ryan J. Taft, Matthew S. Lebo, Jillian G. Buchan, Steven M. Harrison, Ross Rowsey, Eric W. Klee, Pengfei Liu, Elizabeth A. Worthey, Vaidehi Jobanputra, David Dimmock, Hutton M. Kearney, David Bick, Shashikant Kulkarni, Stacie L. Taylor, John W. Belmont, Dimitri J. Stavropoulos, Niall J. Lennon	85
12	Clinical utility of genomic sequencing: a measurement toolkit 2020 ·npj Genomic Medicine ·Robin Z. Hayeems, David Dimmock, David Bick, John W. Belmont, Robert C. Green, Brendan C. Lanpher, Vaidehi Jobanputra, Roberto Mendoza‐Londono, (unknown), Megan E. Grove, Stacie L. Taylor, Euan A. Ashley	46
13	An online compendium of treatable genetic disorders 2020 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·David Bick, (unknown), David Dimmock, Tom Fowler, Mark J. Caulfield, Richard H. Scott	43
14	The Medical Genome Initiative: moving whole-genome sequencing for rare disease diagnosis to the clinic 2020 ·Genome Medicine ·Christian R. Marshall, David Bick, John W. Belmont, Stacie L. Taylor, Euan A. Ashley, David Dimmock, Vaidehi Jobanputra, Hutton M. Kearney, Shashikant Kulkarni, Heidi L. Rehm	27
15	Postmortem diagnosis of PPA2-associated sudden cardiac death from dried blood spot in a neonate presenting with vocal cord paralysis 2020 ·Molecular Case Studies ·Erica Sanford Kobayashi, Marilyn C. Jones, Matthew T. Brigger, Monia Hammer, (unknown), Stephen F. Kingsmore, David Dimmock, Matthew N. Bainbridge	10
16	Biallelic loss of GNAS in a patient with pediatric medulloblastoma 2019 ·Molecular Case Studies ·Mari Tokita, Shareef Nahas, Benjamin Briggs, Denise Malicki, Jill P. Mesirov, Iris Reyes, Lauge Farnaes, Michael L. Levy, Stephen F. Kingsmore, David Dimmock, John R. Crawford, Robert J. Wechsler‐Reya	6
17	Novel Factor XIII variant identified through whole-genome sequencing in a child with intracranial hemorrhage 2018 ·Molecular Case Studies ·Benjamin Briggs, Kiely N. James, Shimul Chowdhury, Courtney D. Thornburg, Lauge Farnaes, David Dimmock, Stephen F. Kingsmore, (unknown)	6
18	Protocol for the “Implementation, adoption, and utility of family history in diverse care settings” study 2015 ·Implementation Science ·(unknown), R. Ryanne Wu, Rachel A. Myers, Catherine A. McCarty, David Dimmock, Michael H. Farrell, Deanna Cross, Troy D. Chinevere, Geoffrey S. Ginsburg, Lori A. Orlando	17
19	Hypertrophic Cardiomyopathy: A New Mutation Illustrates the Need for Family-Centered Care 2014 ·Pediatric Cardiology ·Daniel J. Lee, Regan Veith, David Dimmock, Margaret M. Samyn	2
20	Quantitative Evaluation of the Mitochondrial DNA Depletion Syndrome 2010 ·Clinical Chemistry ·David Dimmock, Lin-ya Tang, Eric Schmitt, Lee‐Jun C. Wong	101

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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