Heather M. McLaughlin

5.2k total citations
33 papers, 1.0k citations indexed

About

Heather M. McLaughlin is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Heather M. McLaughlin has authored 33 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Heather M. McLaughlin's work include Genomics and Rare Diseases (9 papers), Cancer Genomics and Diagnostics (4 papers) and RNA and protein synthesis mechanisms (4 papers). Heather M. McLaughlin is often cited by papers focused on Genomics and Rare Diseases (9 papers), Cancer Genomics and Diagnostics (4 papers) and RNA and protein synthesis mechanisms (4 papers). Heather M. McLaughlin collaborates with scholars based in United States, Canada and United Kingdom. Heather M. McLaughlin's co-authors include Anthony Antonellis, Stephan Züchner, Matthew S. Lebo, Heidi L. Rehm, Robert C. Green, Hatice Duzkale, Jun Shen, Jeffery M. Vance, Kevin Talbot and Leslie G. Biesecker and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Journal of Allergy and Clinical Immunology.

In The Last Decade

Heather M. McLaughlin

31 papers receiving 984 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Heather M. McLaughlin United States	16	517	298	181	117	77	33	1.0k
Sarah L. Sawyer Canada	15	589 1.1×	486 1.6×	99 0.5×	80 0.7×	26 0.3×	37	1.0k
Brendan C. Lanpher United States	17	581 1.1×	465 1.6×	64 0.4×	40 0.3×	37 0.5×	41	1.2k
Bilal N. Sheikh Australia	19	804 1.6×	186 0.6×	65 0.4×	104 0.9×	22 0.3×	39	1.1k
Rui Kan China	14	511 1.0×	182 0.6×	119 0.7×	50 0.4×	33 0.4×	26	816
Jean-Louis Danan France	22	559 1.1×	264 0.9×	62 0.3×	169 1.4×	30 0.4×	41	1.0k
Sally Heywood United Kingdom	4	798 1.5×	504 1.7×	55 0.3×	91 0.8×	21 0.3×	8	1.4k
Dorota Piekutowska‐Abramczuk Poland	17	773 1.5×	181 0.6×	24 0.1×	86 0.7×	27 0.4×	59	1.0k
Sebastian A. Lewandowski Sweden	12	389 0.8×	387 1.3×	60 0.3×	168 1.4×	6 0.1×	18	925
Nadejda Valtcheva Switzerland	12	508 1.0×	70 0.2×	51 0.3×	169 1.4×	12 0.2×	16	1.1k

Countries citing papers authored by Heather M. McLaughlin

Since Specialization

Citations

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

Fields of papers citing papers by Heather M. McLaughlin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heather M. McLaughlin

This figure shows the co-authorship network connecting the top 25 collaborators of Heather M. McLaughlin. A scholar is included among the top collaborators of Heather M. McLaughlin 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 Heather M. McLaughlin. Heather M. McLaughlin 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

Upton, Julia, et al.. (2025). Clinical and genetic findings of individuals tested using the navigateAPDS genetic testing program. Annals of Allergy Asthma & Immunology. 136(2). 213–220.e5.

MacCarrick, Gretchen, Swaroop Aradhya, Emanuela Izzo, et al.. (2024). Clinical utility of comprehensive gene panel testing for common and rare causes of skeletal dysplasia and other skeletal disorders: Results from the largest cohort to date. American Journal of Medical Genetics Part A. 194(9). e63646–e63646. 1 indexed citations

Büsch, Katharina, et al.. (2024). Genetic Etiologies and Outcomes in Malignancy and Mortality in Activated Phosphoinositide 3-Kinase Delta Syndrome: A Systematic Review. Advances in Therapy. 42(2). 752–771. 1 indexed citations

McLaughlin, Heather M., et al.. (2024). Disparities in Genetic Testing for Inborn Errors of Immunity. The Journal of Allergy and Clinical Immunology In Practice. 13(2). 388–395.e3. 2 indexed citations

Rheault, Michelle N., Heather M. McLaughlin, Lauren E. Blake, et al.. (2023). COL4A gene variants are common in children with hematuria and a family history of kidney disease. Pediatric Nephrology. 38(11). 3625–3633. 5 indexed citations

McLaughlin, Heather M., et al.. (2021). Noncanonical Auxin Signaling. Cold Spring Harbor Perspectives in Biology. 13(5). a039917–a039917. 13 indexed citations

Gripp, Karen W., Sarah Smithson, Ingrid Scurr, et al.. (2021). Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3—a subgroup of K+ channelopathies. European Journal of Human Genetics. 29(9). 1384–1395. 25 indexed citations

Machini, Kalotina, Ozge Ceyhan‐Birsoy, Danielle R. Azzariti, et al.. (2019). Analyzing and Reanalyzing the Genome: Findings from the MedSeq Project. The American Journal of Human Genetics. 105(1). 177–188. 26 indexed citations

Costantini, Alice, Helena Valta, Nissan Baratang, et al.. (2018). Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with “corner fractures”. Bone. 121. 163–171. 12 indexed citations

10.

Suzuki, Yoshiro, David Chitayat, Hirotake Sawada, et al.. (2018). TRPV6 Variants Interfere with Maternal-Fetal Calcium Transport through the Placenta and Cause Transient Neonatal Hyperparathyroidism. The American Journal of Human Genetics. 102(6). 1104–1114. 54 indexed citations

11.

Koboldt, Daniel C., Megan A. Waldrop, Benjamin Kelly, et al.. (2018). In-frame de novo mutation in BICD2 in two patients with muscular atrophy and arthrogryposis. Molecular Case Studies. 4(5). a003160–a003160. 13 indexed citations

12.

Vassy, Jason L., Denise Lautenbach, Heather M. McLaughlin, et al.. (2014). The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine. Trials. 15(1). 85–85. 102 indexed citations

13.

McLaughlin, Heather M., Reiko Sakaguchi, William Giblin, et al.. (2014). A Recurrent Loss-of-Function Alanyl-tRNA Synthetase (AARS) Mutation in Patients with Charcot-Marie-Tooth Disease Type 2N (CMT2N). Human Mutation. 35(4). 512–512. 1 indexed citations

14.

Vester, Aimée, Heather M. McLaughlin, James R. Lupski, et al.. (2013). A Loss-of-Function Variant in the Human Histidyl-tRNA Synthetase (HARS) Gene is Neurotoxic In Vivo. Oxford University Research Archive (ORA) (University of Oxford). 4 indexed citations

15.

McLaughlin, Heather M., Melissa Kelly, Pamela Hawley, et al.. (2013). Compound heterozygosity of predicted loss-of-function DESvariants in a family with recessive desminopathy. BMC Medical Genetics. 14(1). 68–68. 20 indexed citations

16.

McLaughlin, Heather M., Reiko Sakaguchi, William Giblin, et al.. (2011). A Recurrent loss-of-function alanyl-tRNA synthetase (AARS ) mutation in patients with charcot-marie-tooth disease type 2N (CMT2N). Human Mutation. 33(1). 244–253. 83 indexed citations

17.

Lega, Iliana C., et al.. (2011). A physician reminder to improve postpartum diabetes screening in women with gestational diabetes mellitus. Diabetes Research and Clinical Practice. 95(3). 352–357. 30 indexed citations

18.

Lipscombe, Lorraine L., Heather M. McLaughlin, Wei Wu, & Denice S. Feig. (2011). Pregnancy planning in women with pregestational diabetes. The Journal of Maternal-Fetal & Neonatal Medicine. 24(9). 1095–1101. 18 indexed citations

19.

LeBleu, Valerie S., Malin Sund, Hikaru Sugimoto, et al.. (2010). Identification of the NC1 Domain of α3 Chain as Critical for α3α4α5 Type IV Collagen Network Assembly. Journal of Biological Chemistry. 285(53). 41874–41885. 18 indexed citations

20.

Stum, Morgane, Heather M. McLaughlin, Erica L. Kleinbrink, et al.. (2010). An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations. Molecular and Cellular Neuroscience. 46(2). 432–443. 57 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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