Lauren Chad

938 total citations
28 papers, 287 citations indexed

About

Lauren Chad is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lauren Chad has authored 28 papers receiving a total of 287 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 8 papers in Public Health, Environmental and Occupational Health and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lauren Chad's work include Genomics and Rare Diseases (16 papers), BRCA gene mutations in cancer (6 papers) and Prenatal Screening and Diagnostics (6 papers). Lauren Chad is often cited by papers focused on Genomics and Rare Diseases (16 papers), BRCA gene mutations in cancer (6 papers) and Prenatal Screening and Diagnostics (6 papers). Lauren Chad collaborates with scholars based in Canada, United States and United Kingdom. Lauren Chad's co-authors include M. Stephen Meyn, Gregory Costain, Pina Bozzo, Robin Z. Hayeems, Roberto Mendoza‐Londono, Ashish Marwaha, Gideon Koren, Anna Pupco, Yvan St‐Pierre and Mary Allen and has published in prestigious journals such as PLoS ONE, Allergy and Journal of Medical Genetics.

In The Last Decade

Lauren Chad

24 papers receiving 277 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lauren Chad Canada 9 99 63 50 46 38 28 287
A. Caretto Italy 12 99 1.0× 127 2.0× 49 1.0× 56 1.2× 81 2.1× 21 449
Hasan Acar Türkiye 12 91 0.9× 35 0.6× 88 1.8× 9 0.2× 62 1.6× 33 315
Karen Agnew New Zealand 11 24 0.2× 136 2.2× 50 1.0× 23 0.5× 58 1.5× 19 387
Katharina Schoner Germany 10 127 1.3× 35 0.6× 113 2.3× 6 0.1× 45 1.2× 20 272
Parag Tamhankar India 10 67 0.7× 20 0.3× 95 1.9× 10 0.2× 16 0.4× 32 272
Kristina Uvebrant Sweden 7 101 1.0× 64 1.0× 73 1.5× 5 0.1× 60 1.6× 9 256
B. Bessières France 12 38 0.4× 23 0.4× 61 1.2× 11 0.2× 41 1.1× 23 352
Paul Sackstein United States 8 18 0.2× 74 1.2× 26 0.5× 36 0.8× 38 1.0× 16 276
Simon Toupance France 11 36 0.4× 58 0.9× 110 2.2× 16 0.3× 40 1.1× 25 418
Randall Li United States 8 20 0.2× 74 1.2× 21 0.4× 185 4.0× 38 1.0× 11 369

Countries citing papers authored by Lauren Chad

Since Specialization
Citations

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

Fields of papers citing papers by Lauren Chad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lauren Chad

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

All Works

20 of 20 papers shown
1.
Abdul‐Rahman, Omar, Giulia Pascolini, Giovanni Di Zenzo, et al.. (2025). Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene. American Journal of Medical Genetics Part A. 197(11). e64171–e64171.
2.
Martimianakis, Maria Athina, Lauren Chad, Karen Leslie, et al.. (2025). The birth of the virtual clinic: welcome to the Mediverse. Advances in Health Sciences Education. 30(4). 1297–1311.
3.
Dolman, Lena, Stephanie Luca, Salma Shickh, et al.. (2025). The Clinician-reported Genetic Testing Utility InDEx for Neonatal Intensive Care (C-GUIDE NICU): Quantifying genome-wide sequencing utility in the NICU. Genetics in Medicine. 27(9). 101503–101503. 1 indexed citations
4.
Mackley, Michael P., Hanna Faghfoury, & Lauren Chad. (2024). Rectifying or Reinforcing? The (In)Equity Implications of Recontacting Practices in Genomic Medicine. The Hastings Center Report. 54(S2). S22–S30. 1 indexed citations
5.
Hayeems, Robin Z., Stephanie Luca, Lauren Chad, et al.. (2024). The Clinician-reported Genetic Testing Utility Index (C-GUIDE) for Prenatal Care: Initial evidence of content and construct validity. Genetics in Medicine. 27(1). 101306–101306. 1 indexed citations
6.
Goh, Elaine, Lauren Chad, Julie Richer, et al.. (2024). Canadian College of Medical Geneticists: clinical practice advisory document – responsibility to recontact for reinterpretation of clinical genetic testing. Journal of Medical Genetics. 61(12). 1123–1131. 2 indexed citations
7.
Lemaire, Mathieu, Damien Noone, Kimberly Liu, et al.. (2024). Diagnosing a genetic disease in a donor-conceived child: case report and discussion of the ethical, legal, and practical issues. Pediatric Nephrology. 40(3). 859–864.
8.
Mackley, Michael P. & Lauren Chad. (2023). Equity implications of patient-initiated recontact and follow-up in clinical genetics. European Journal of Human Genetics. 31(5). 495–496. 3 indexed citations
9.
Hayeems, Robin Z., Stephanie Luca, Lauren Chad, et al.. (2023). Assessing the Performance of the Clinician-reported Genetic Testing Utility InDEx (C-GUIDE): Further Evidence of Inter-rater Reliability. Clinical Therapeutics. 45(8). 729–735. 2 indexed citations
10.
Hayeems, Robin Z., Stephanie Luca, Anna Hurst, et al.. (2022). Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validity. European Journal of Human Genetics. 30(12). 1423–1431. 9 indexed citations
11.
Awamleh, Zain, Eric Chater‐Diehl, Sanaa Choufani, et al.. (2022). DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes. European Journal of Human Genetics. 30(6). 695–702. 14 indexed citations
12.
Marwaha, Ashish, Gregory Costain, Cheryl Cytrynbaum, et al.. (2022). The utility of DNA methylation signatures in directing genome sequencing workflow: Kabuki syndrome and CDK13‐related disorder. American Journal of Medical Genetics Part A. 188(5). 1368–1375. 6 indexed citations
13.
Chad, Lauren & Michael J. Szego. (2021). Please give me a copy of my child’s raw genomic data. npj Genomic Medicine. 6(1). 15–15. 1 indexed citations
14.
Marwaha, Ashish, David Chitayat, M. Stephen Meyn, Roberto Mendoza‐Londono, & Lauren Chad. (2021). The point‐of‐care use of a facial phenotyping tool in the genetics clinic: Enhancing diagnosis and education with machine learning. American Journal of Medical Genetics Part A. 185(4). 1151–1158. 26 indexed citations
15.
Chad, Lauren, Angelika J. Dawson, & Elaine Goh. (2020). Canadian College of Medical Geneticists (CCMG) points to consider: resuming genetic services in a pandemic—a summary. Journal of Medical Genetics. 59(1). 101–104. 2 indexed citations
16.
Hayeems, Robin Z., Stephanie Luca, Wendy J. Ungar, et al.. (2019). The development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE): a novel strategy for measuring the clinical utility of genetic testing. Genetics in Medicine. 22(1). 95–101. 22 indexed citations
17.
Chad, Lauren, Anna Pupco, Pina Bozzo, & Gideon Koren. (2013). Update on antidepressant use during breastfeeding.. PubMed. 59(6). 633–4. 23 indexed citations
18.
Chad, Lauren, Moshe Ben‐Shoshan, Yuka Asai, et al.. (2013). A majority of parents of children with peanut allergy fear using the epinephrine auto-injector. Allergy. 68(12). 1605–1609. 48 indexed citations
19.
Graham, Deborah S. Cunninghame, Timothy J. Vyse, Paul R. Fortin, et al.. (2008). Association of LY9 in UK and Canadian SLE families. Genes and Immunity. 9(2). 93–102. 64 indexed citations
20.
Zogopoulos, George, Claus Jørgensen, Julinor Bacani, et al.. (2008). Germline EPHB2 Receptor Variants in Familial Colorectal Cancer. PLoS ONE. 3(8). e2885–e2885. 14 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by A. Caretto Breakdown of academic impact, for papers by Hasan Acar Breakdown of academic impact, for papers by Karen Agnew Breakdown of academic impact, for papers by Katharina Schoner Breakdown of academic impact, for papers by Parag Tamhankar Breakdown of academic impact, for papers by Kristina Uvebrant Breakdown of academic impact, for papers by B. Bessières Breakdown of academic impact, for papers by Paul Sackstein Breakdown of academic impact, for papers by Simon Toupance Breakdown of academic impact, for papers by Randall Li
Rankless by CCL
2026