Mary Ann Thomas

766 total citations
46 papers, 361 citations indexed

About

Mary Ann Thomas is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mary Ann Thomas has authored 46 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 12 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mary Ann Thomas's work include Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (9 papers) and Cleft Lip and Palate Research (6 papers). Mary Ann Thomas is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (9 papers) and Cleft Lip and Palate Research (6 papers). Mary Ann Thomas collaborates with scholars based in Canada, United States and India. Mary Ann Thomas's co-authors include Vazken M. Der Kaloustian, Christine M. Armour, Jo‐Ann Brock, Tanya N. Nelson, Shelley Dougan, Jane Evans, Frédérique Tihy, William T. Gibson, Elena Kolomietz and Dimitri J. Stavropoulos and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and The Journal of Pediatrics.

In The Last Decade

Mary Ann Thomas

44 papers receiving 342 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mary Ann Thomas Canada 10 180 126 123 47 45 46 361
Rhoda Cameron Australia 7 213 1.2× 38 0.3× 174 1.4× 8 0.2× 67 1.5× 15 463
Birsen Karaman Türkiye 12 157 0.9× 57 0.5× 180 1.5× 9 0.2× 64 1.4× 58 345
M Chaâbouni Tunisia 12 133 0.7× 26 0.2× 108 0.9× 53 1.1× 19 0.4× 43 369
R. Rauskolb Germany 14 128 0.7× 196 1.6× 82 0.7× 11 0.2× 99 2.2× 41 379
Jacob S. Hogue United States 9 119 0.7× 50 0.4× 186 1.5× 9 0.2× 118 2.6× 21 340
Barbara Sibbles Netherlands 9 70 0.4× 28 0.2× 121 1.0× 5 0.1× 70 1.6× 12 283
Luca Barbieri Italy 13 51 0.3× 29 0.2× 143 1.2× 109 2.3× 10 0.2× 20 350
Jacques Battin France 7 91 0.5× 37 0.3× 76 0.6× 9 0.2× 34 0.8× 13 249
L.C. Stranc Canada 7 67 0.4× 38 0.3× 86 0.7× 12 0.3× 52 1.2× 10 230
M. Barr United States 6 144 0.8× 93 0.7× 199 1.6× 6 0.1× 62 1.4× 6 346

Countries citing papers authored by Mary Ann Thomas

Since Specialization
Citations

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

Fields of papers citing papers by Mary Ann Thomas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary Ann Thomas. 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 Mary Ann Thomas. The network helps show where Mary Ann Thomas may publish in the future.

Co-authorship network of co-authors of Mary Ann Thomas

This figure shows the co-authorship network connecting the top 25 collaborators of Mary Ann Thomas. A scholar is included among the top collaborators of Mary Ann Thomas 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 Mary Ann Thomas. Mary Ann Thomas 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.
Thomas, Mary Ann, Susan Crawford, & Tanya Bedard. (2025). A Population‐Based Study of Limb Body Wall Complex With Proposed Features for Prenatal Diagnosis. American Journal of Medical Genetics Part A. 197(11). e64140–e64140.
2.
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
3.
4.
Wickwire, Emerson M., Jacob Collen, Vincent F. Capaldi, et al.. (2023). Patient Engagement and Provider Effectiveness of a Novel Sleep Telehealth Platform and Remote Monitoring Assessment in the US Military: Pilot Study Providing Evidence-Based Sleep Treatment Recommendations. JMIR Formative Research. 7. e47356–e47356. 1 indexed citations
5.
Lowry, R. Brian, Tanya Bedard, Susan Crawford, et al.. (2023). The Alberta Congenital Anomalies Surveillance System: a 40-year review with prevalence and trends for selected congenital anomalies, 1997–2019. Health Promotion and Chronic Disease Prevention in Canada. 43(1). 40–48. 6 indexed citations
6.
Lowry, R. Brian, Tanya Bedard, Susan Crawford, et al.. (2023). Le système de surveillance des anomalies congénitales de l’Alberta : compte rendu des données sur 40 ans avec prévalence et tendances de certaines anomalies congénitales entre 1997 et 2019. SHILAP Revista de lepidopterología. 43(1). 42–51. 2 indexed citations
7.
Petrin, Aline, Erliang Zeng, Mary Ann Thomas, et al.. (2023). DNA methylation differences in monozygotic twins with Van der Woude syndrome. SHILAP Revista de lepidopterología. 4. 2 indexed citations
8.
Thomas, Mary Ann, et al.. (2023). Craniofacial Microsomia, Associated Congenital Anomalies, and Risk Factors in 63 Cases from the Alberta Congenital Anomalies Surveillance System. The Journal of Pediatrics. 261. 113528–113528. 2 indexed citations
9.
Lee, Se Won, et al.. (2021). Conservative Management of Low Back Pain. HCA Healthcare Journal of Medicine. 2(5). 319–328. 4 indexed citations
10.
Parboosingh, Jillian S., et al.. (2020). Re-evaluating the first-tier status of fragile X testing in neurodevelopmental disorders. Genetics in Medicine. 22(6). 1036–1039. 19 indexed citations
11.
Thomas, Mary Ann, et al.. (2019). Dermoscopy of keratosis pilaris. Indian Dermatology Online Journal. 10(5). 613–613. 7 indexed citations
12.
Verma, Shyam B., Resham Vasani, Laxmisha Chandrashekar, & Mary Ann Thomas. (2017). Seborrheic melanosis: An entity worthy of mention in dermatological literature. Indian Journal of Dermatology Venereology and Leprology. 83(3). 285–285. 9 indexed citations
13.
Lazier, Joanna, Deborah Fruitman, Julie Lauzon, et al.. (2016). Prenatal Array Comparative Genomic Hybridization in Fetuses With Structural Cardiac Anomalies. Journal of Obstetrics and Gynaecology Canada. 38(7). 619–626. 11 indexed citations
14.
Thomas, Mary Ann & Uday Khopkar. (2016). Salute sign: A nonambiguous histopathological sign in pityriasis rosea. Indian Dermatology Online Journal. 7(6). 543–543. 4 indexed citations
15.
Lazier, Joanna, Jean K. Mah, Ana Nikolić, et al.. (2015). Bilateral congenital lumbar hernias in a patient with central core disease – A case report. Neuromuscular Disorders. 26(1). 56–59. 5 indexed citations
16.
Alaimo, Joseph T., Sureni V. Mullegama, Mary Ann Thomas, & Sarah H. Elsea. (2015). Copy number loss upstream of RAI1 uncovers gene expression regulatory region that may impact Potocki–Lupski syndrome diagnosis. Molecular Cytogenetics. 8(1). 75–75. 5 indexed citations
17.
Thomas, Mary Ann, et al.. (2012). Keratosis Pilaris Revisited: Is It More Than Just a Follicular Keratosis?. International Journal of Trichology. 4(4). 255–255. 32 indexed citations
18.
Jobling, Rebekah, et al.. (2011). Monozygotic twins with variable expression of Van der Woude Syndrome. American Journal of Medical Genetics Part A. 155(8). 2008–2010. 9 indexed citations
19.
Thomas, Mary Ann, Vazken M. Der Kaloustian, & Ted L. Tewfik. (2004). Connexin Mutation Testing of Children with Nonsyndromic, Autosomal Recessive Sensorineural Hearing Loss. The Journal of Otolaryngology. 33(3). 189–189. 2 indexed citations
20.
Thomas, Mary Ann, Alessandra M.V. Duncan, Claudette Bardin, & Vazken M. Der Kaloustian. (2003). Lissencephaly with der(17)t(17;20)(p13.3;p12.2)mat. American Journal of Medical Genetics Part A. 124A(3). 292–295. 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.

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