Shweta U. Dhar

3.9k total citations
31 papers, 583 citations indexed

About

Shweta U. Dhar is a scholar working on Genetics, Molecular Biology and Clinical Psychology. According to data from OpenAlex, Shweta U. Dhar has authored 31 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 9 papers in Molecular Biology and 8 papers in Clinical Psychology. Recurrent topics in Shweta U. Dhar's work include BRCA gene mutations in cancer (10 papers), Autism Spectrum Disorder Research (8 papers) and Family and Disability Support Research (8 papers). Shweta U. Dhar is often cited by papers focused on BRCA gene mutations in cancer (10 papers), Autism Spectrum Disorder Research (8 papers) and Family and Disability Support Research (8 papers). Shweta U. Dhar collaborates with scholars based in United States, China and Taiwan. Shweta U. Dhar's co-authors include Lei‐Shih Chen, Lei Xu, Tanya N. Eble, Tse‐Yang Huang, Sharon E. Plon, H. Paul Cooper, Susan G. Hilsenbeck, Oi‐Man Kwok, Lorraine Potocki and Eunju Jung and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Bone and Joint Surgery and American Journal of Preventive Medicine.

In The Last Decade

Shweta U. Dhar

31 papers receiving 578 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shweta U. Dhar United States 16 368 173 154 100 97 31 583
Charles M. Strom United States 16 357 1.0× 119 0.7× 241 1.6× 132 1.3× 23 0.2× 37 883
David J. Aughton United States 15 494 1.3× 71 0.4× 313 2.0× 178 1.8× 37 0.4× 30 815
Mercy Laurino United States 13 245 0.7× 63 0.4× 99 0.6× 138 1.4× 34 0.4× 31 548
Heidi Cope United States 15 291 0.8× 141 0.8× 148 1.0× 88 0.9× 57 0.6× 37 615
Tanya N. Eble United States 13 250 0.7× 54 0.3× 214 1.4× 132 1.3× 26 0.3× 24 473
Karen E. Wain United States 14 378 1.0× 64 0.4× 120 0.8× 123 1.2× 19 0.2× 28 567
Samantha A. Schrier Vergano United States 18 331 0.9× 48 0.3× 451 2.9× 85 0.8× 14 0.1× 52 736
Gabrielle J. Halpern Israel 13 243 0.7× 120 0.7× 406 2.6× 80 0.8× 28 0.3× 23 737
C D Boehm United States 15 459 1.2× 107 0.6× 537 3.5× 184 1.8× 22 0.2× 18 1.5k
Alina T. Midro Poland 16 575 1.6× 72 0.4× 436 2.8× 244 2.4× 16 0.2× 74 943

Countries citing papers authored by Shweta U. Dhar

Since Specialization
Citations

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

Fields of papers citing papers by Shweta U. Dhar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shweta U. Dhar. 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 Shweta U. Dhar. The network helps show where Shweta U. Dhar may publish in the future.

Co-authorship network of co-authors of Shweta U. Dhar

This figure shows the co-authorship network connecting the top 25 collaborators of Shweta U. Dhar. A scholar is included among the top collaborators of Shweta U. Dhar 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 Shweta U. Dhar. Shweta U. Dhar 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.
McDonald, Malcolm F., Ethan B. Ludmir, Shlomit Yust‐Katz, et al.. (2023). Prevalence of pathogenic germline variants in adult-type diffuse glioma. Neuro-Oncology Practice. 10(5). 482–490. 1 indexed citations
2.
Chen, Wei‐Ju, Oi‐Man Kwok, Shweta U. Dhar, et al.. (2021). Psychometric Properties of the POAGTS: A Tool for Understanding Parents’ Perceptions Regarding Autism Spectrum Disorder Genetic Testing. International Journal of Environmental Research and Public Health. 18(6). 3323–3323. 3 indexed citations
3.
Yang, Yu, Shweta U. Dhar, Jennifer M. Taylor, & Bhuvaneswari Krishnan. (2021). Papillary Renal Cell Carcinoma in Lynch/Muir-Torre Syndrome with Germline Pathogenic Variant in MSH6 and Molecular Analysis: Report of a Case and Review of the Literature. SHILAP Revista de lepidopterología. 8(2). 8–19. 1 indexed citations
4.
Jacobs, Ryan C, et al.. (2020). Implementation of a Medical School Elective Course Incorporating Case-Based Learning: a Pilot Study. Medical Science Educator. 30(1). 339–344. 5 indexed citations
5.
Chen, Lei‐Shih, et al.. (2020). Texas Health Educators’ Practice in Basic Genomics Education and Services. Personalized Medicine. 18(1). 55–66. 1 indexed citations
6.
Eble, Tanya N., et al.. (2020). Financial barriers in a county genetics clinic: Problems and solutions. Journal of Genetic Counseling. 29(4). 678–688. 15 indexed citations
7.
Chen, Wei‐Ju, et al.. (2020). Family Health History–Based Cancer Prevention Training for Community Health Workers. American Journal of Preventive Medicine. 60(3). e159–e167. 3 indexed citations
8.
Chen, Wei‐Ju, et al.. (2020). Pursuing genetic testing for children with autism spectrum disorders: What do parents think?. Journal of Genetic Counseling. 30(2). 370–382. 11 indexed citations
9.
Batzir, Nurit Assia, Tanya N. Eble, Pengfei Liu, et al.. (2019). De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures. Molecular Case Studies. 5(3). a003673–a003673. 26 indexed citations
10.
Chen, Wei‐Ju, et al.. (2019). Genetic Testing Experiences Among Parents of Children with Autism Spectrum Disorder in the United States. Journal of Autism and Developmental Disorders. 49(12). 4821–4833. 23 indexed citations
11.
Prakash, Preeti, Tanya N. Eble, & Shweta U. Dhar. (2018). Quality improvement of clinic flow for complex genetic conditions: Using Ehlers–Danlos syndrome as a model. Molecular Genetics & Genomic Medicine. 6(6). 993–1000. 3 indexed citations
12.
Chen, Lei‐Shih, et al.. (2018). Development and evaluation of a genomics training program for community health workers in Texas. Genetics in Medicine. 20(9). 1030–1037. 15 indexed citations
13.
Li, Ming, Ann O. Amuta, Lei Xu, et al.. (2016). Autism genetic testing information needs among parents of affected children: A qualitative study. Patient Education and Counseling. 99(6). 1011–1016. 22 indexed citations
14.
Chen, Lei‐Shih, Lei Xu, Tse‐Yang Huang, & Shweta U. Dhar. (2013). Autism genetic testing: a qualitative study of awareness, attitudes, and experiences among parents of children with autism spectrum disorders. Genetics in Medicine. 15(4). 274–281. 71 indexed citations
15.
Dhar, Shweta U., Raye Lynn Alford, Elizabeth A. Nelson, & Lorraine Potocki. (2012). Enhancing exposure to genetics and genomics through an innovative medical school curriculum. Genetics in Medicine. 14(1). 163–167. 35 indexed citations
16.
Bacino, Carlos A., Shweta U. Dhar, Nicola Brunetti‐Pierri, Brendan Lee, & Penelope E. Bonnen. (2012). WDR35 mutation in siblings with Sensenbrenner syndrome: A ciliopathy with variable phenotype. American Journal of Medical Genetics Part A. 158A(11). 2917–2924. 37 indexed citations
17.
Eble, Tanya N., Sandesh C.S. Nagamani, Luis M. Franco, et al.. (2012). The practice of adult genetics: A 7‐year experience from a single center. American Journal of Medical Genetics Part A. 161(1). 89–93. 5 indexed citations
18.
Plon, Sharon E., H. Paul Cooper, Shweta U. Dhar, et al.. (2011). Genetic testing and cancer risk management recommendations by physicians for at-risk relatives. Genetics in Medicine. 13(2). 148–154. 80 indexed citations
19.
Dhar, Shweta U., Patricia Robbins‐Furman, Moise L. Levy, Ankita Patel, & Fernando Scaglia. (2009). Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty. American Journal of Medical Genetics Part A. 149A(5). 993–996. 12 indexed citations
20.
Dhar, Shweta U., Fernando Scaglia, Laurie D. Smith, et al.. (2008). Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiency. Molecular Genetics and Metabolism. 96(1). 38–43. 45 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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