Michelle M. Clark

2.7k total citations · 2 hit papers
17 papers, 1.1k citations indexed

About

Michelle M. Clark is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Michelle M. Clark has authored 17 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 2 papers in Surgery and 2 papers in Molecular Biology. Recurrent topics in Michelle M. Clark's work include Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic factors in colorectal cancer (2 papers). Michelle M. Clark is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic factors in colorectal cancer (2 papers). Michelle M. Clark collaborates with scholars based in United States, Australia and United Kingdom. Michelle M. Clark's co-authors include Stephen F. Kingsmore, David Dimmock, Lauge Farnaes, Tiong Yang Tan, Susan M. White, Zornitza Stark, Julie A. Cakici, Nathaly M. Sweeney, Narayanan Veeraraghavan and Shimul Chowdhury and has published in prestigious journals such as The American Journal of Human Genetics, Molecular Ecology and Clinical Therapeutics.

In The Last Decade

Michelle M. Clark

17 papers receiving 1.1k 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 Michelle M. Clark, Zornitza Stark et al. npj Genomic Medicine profile →
Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization

2018 280 citations Lauge Farnaes, Amber Hildreth et al. npj Genomic Medicine profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Michelle M. Clark United States	10	896	360	161	160	135	17	1.1k
Shimul Chowdhury United States	16	660 0.7×	378 1.1×	116 0.7×	158 1.0×	121 0.9×	32	1.0k
Tanya N. Nelson Canada	21	450 0.5×	308 0.9×	84 0.5×	276 1.7×	72 0.5×	51	1.0k
Erin Rooney Riggs United States	14	950 1.1×	462 1.3×	89 0.6×	377 2.4×	153 1.1×	21	1.3k
Karen L. David United States	12	491 0.5×	263 0.7×	59 0.4×	226 1.4×	60 0.4×	14	899
Guido M. W. R. de Wert Netherlands	13	621 0.7×	198 0.6×	76 0.5×	500 3.1×	140 1.0×	20	1.2k
Charles M. Strom United States	16	357 0.4×	241 0.7×	34 0.2×	132 0.8×	85 0.6×	37	883
Julie Richer Canada	13	399 0.4×	202 0.6×	32 0.2×	89 0.6×	55 0.4×	34	670
Christine M. Armour Canada	20	435 0.5×	340 0.9×	27 0.2×	358 2.2×	68 0.5×	52	923
Derek Lim United Kingdom	13	546 0.6×	651 1.8×	74 0.5×	293 1.8×	70 0.5×	24	928
Emanuele Agolini Italy	16	327 0.4×	479 1.3×	61 0.4×	47 0.3×	46 0.3×	82	989

Countries citing papers authored by Michelle M. Clark

Since Specialization

Citations

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

Fields of papers citing papers by Michelle M. Clark

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michelle M. Clark. 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 Michelle M. Clark. The network helps show where Michelle M. Clark may publish in the future.

Co-authorship network of co-authors of Michelle M. Clark

This figure shows the co-authorship network connecting the top 25 collaborators of Michelle M. Clark. A scholar is included among the top collaborators of Michelle M. Clark 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 Michelle M. Clark. Michelle M. Clark is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

Cakici, Julie A., David Dimmock, Sara Caylor, et al.. (2023). Assessing Diversity in Newborn Genomic Sequencing Research Recruitment: Race/Ethnicity and Primary Spoken Language Variation in Eligibility, Enrollment, and Reasons for Declining. Clinical Therapeutics. 45(8). 736–744. 7 indexed citations

Sweeney, Nathaly M., Shareef Nahas, Shimul Chowdhury, et al.. (2021). Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease. npj Genomic Medicine. 6(1). 29–29. 49 indexed citations

Clark, Michelle M., et al.. (2020). Species-specific evaluation of 2 patients with suspected crab allergy. The Journal of Allergy and Clinical Immunology In Practice. 9(1). 511–513. 1 indexed citations

James, Kiely N., Michelle M. Clark, Cyrielle Kint, et al.. (2020). Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses. npj Genomic Medicine. 5(1). 33–33. 32 indexed citations

Cakici, Julie A., David Dimmock, Sara Caylor, et al.. (2020). A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants. The American Journal of Human Genetics. 107(5). 953–962. 66 indexed citations

Kingsmore, Stephen F., Mallory Owen, Michelle M. Clark, et al.. (2020). Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing. npj Genomic Medicine. 5(1). 49–49. 34 indexed citations

Kobayashi, Erica Sanford, Michelle M. Clark, Lauge Farnaes, et al.. (2019). Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICU*. Pediatric Critical Care Medicine. 20(11). 1007–1020. 88 indexed citations

Clark, Michelle M. & Robin Featherstone. (2019). Management of Acute Withdrawal and Detoxification for Adults who Misuse Methamphetamine: A Review of the Clinical Evidence and Guidelines. 2 indexed citations

Clark, Michelle M., et al.. (2019). Antisepsis for Urinary Catheter Insertion: A Review of Clinical Effectiveness and Guidelines. 4 indexed citations

10.

Farnaes, Lauge, Amber Hildreth, Nathaly M. Sweeney, et al.. (2018). Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization. npj Genomic Medicine. 3(1). 10–10. 280 indexed citations breakdown →

11.

Clark, Michelle M., Zornitza Stark, Lauge Farnaes, et al.. (2018). Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases. npj Genomic Medicine. 3(1). 16–16. 340 indexed citations breakdown →

12.

Petrikin, Josh E, Julie A. Cakici, Michelle M. Clark, et al.. (2018). The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants. npj Genomic Medicine. 3(1). 6–6. 137 indexed citations

13.

Clark, Michelle M., et al.. (2018). Honey for Wound Management: A Review of Clinical Effectiveness and Guidelines [Internet]. 1 indexed citations

14.

Clark, Michelle M., et al.. (2018). Honey for Wound Management: A Review of Clinical Effectiveness and Guidelines. Europe PMC (PubMed Central). 6 indexed citations

15.

Clark, Michelle M., Olympe Chazara, Eric M. Sobel, et al.. (2016). Human Birth Weight and Reproductive Immunology: Testing for Interactions between Maternal and Offspring KIR and HLA-C Genes. Human Heredity. 81(4). 181–193. 9 indexed citations

16.

Clark, Michelle M., John Blangero, Thomas D. Dyer, Eric M. Sobel, & Janet S. Sinsheimer. (2015). The Quantitative-MFG Test: A Linear Mixed Effect Model to Detect Maternal-Offspring Gene Interactions. Annals of Human Genetics. 80(1). 63–80. 3 indexed citations

17.

Koch, Ilana J., Michelle M. Clark, Michael J. Thompson, et al.. (2015). The concerted impact of domestication and transposon insertions on methylation patterns between dogs and grey wolves. Molecular Ecology. 25(8). 1838–1855. 50 indexed citations

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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