Mary Beth Dinulos

2.5k total citations
21 papers, 1.3k citations indexed

About

Mary Beth Dinulos is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Mary Beth Dinulos has authored 21 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Mary Beth Dinulos's work include Genomics and Rare Diseases (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Viral gastroenteritis research and epidemiology (2 papers). Mary Beth Dinulos is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Viral gastroenteritis research and epidemiology (2 papers). Mary Beth Dinulos collaborates with scholars based in United States, United Kingdom and Netherlands. Mary Beth Dinulos's co-authors include Christine M. Distèche, Laura Brown, Renee A. Reijo Pera, Otto Daniëls, Bernd Wollnik, Robert E. Shapiro, Jeffrey W. Innis, Catherine E. Keegan, Simeon A. Boyadjiev and Mark Hannibal and has published in prestigious journals such as Nature Genetics, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Mary Beth Dinulos

20 papers receiving 1.2k 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 Beth Dinulos United States 14 892 722 261 141 72 21 1.3k
Patricia Taillon‐Miller United States 21 1.1k 1.2× 895 1.2× 378 1.4× 187 1.3× 80 1.1× 35 2.0k
Elaine R. Levy United Kingdom 19 860 1.0× 857 1.2× 86 0.3× 224 1.6× 30 0.4× 34 1.6k
Édouard W. Khandjian Canada 28 1.8k 2.0× 1.0k 1.4× 146 0.6× 73 0.5× 244 3.4× 44 2.3k
Ulrike C. Lange Germany 15 1.3k 1.5× 354 0.5× 94 0.4× 111 0.8× 182 2.5× 24 1.6k
Cornelia Schmidt Germany 21 657 0.7× 459 0.6× 55 0.2× 173 1.2× 25 0.3× 42 1.2k
David C. Page United States 12 940 1.1× 917 1.3× 237 0.9× 212 1.5× 95 1.3× 17 1.4k
Anne Segonds-Pichon United Kingdom 19 872 1.0× 340 0.5× 72 0.3× 52 0.4× 148 2.1× 38 1.3k
John Cobb United States 21 1.4k 1.6× 533 0.7× 240 0.9× 274 1.9× 381 5.3× 36 1.9k
Hidehito Inagaki Japan 25 1.4k 1.6× 713 1.0× 96 0.4× 392 2.8× 202 2.8× 98 2.1k

Countries citing papers authored by Mary Beth Dinulos

Since Specialization
Citations

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

Fields of papers citing papers by Mary Beth Dinulos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mary Beth Dinulos

This figure shows the co-authorship network connecting the top 25 collaborators of Mary Beth Dinulos. A scholar is included among the top collaborators of Mary Beth Dinulos 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 Beth Dinulos. Mary Beth Dinulos 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.
Rose, Nancy C., Michele Caggana, Mary Beth Dinulos, et al.. (2025). The importance of residual newborn screening dried blood spots, 2025 revision: A position statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 27(8). 101433–101433.
2.
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
3.
Dinulos, Mary Beth & Stephanie E. Vallee. (2020). The Impact of Direct-to-Consumer Genetic Testing on Patient and Provider. Clinics in Laboratory Medicine. 40(1). 61–67. 10 indexed citations
4.
Jung, Hou-Sung, Stephanie E. Vallee, Mary Beth Dinulos, Gregory J. Tsongalis, & Joel A. Lefferts. (2018). Maternally inherited 133kb deletion of 14q32 causing Kagami–Ogata syndrome. Journal of Human Genetics. 63(12). 1231–1239. 7 indexed citations
5.
Cheng, Andrew, Mary Beth Dinulos, Whitney Neufeld‐Kaiser, et al.. (2017). 6q25.1 (TAB2) microdeletion syndrome: Congenital heart defects and cardiomyopathy. American Journal of Medical Genetics Part A. 173(7). 1848–1857. 30 indexed citations
6.
You, Jing, Nara Sobreira, Dustin L. Gable, et al.. (2016). A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2 , a Gene Encoding a Component of the TTT Complex. The American Journal of Human Genetics. 98(5). 909–918. 26 indexed citations
7.
Moeschler, John B., Roberto Amato, Leah W. Burke, et al.. (2009). Improving genetic health care: A Northern New England pilot project addressing the genetic evaluation of the child with developmental delays or intellectual disability. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 151C(3). 241–254. 13 indexed citations
8.
Paznekas, William A., Simeon A. Boyadjiev, Robert E. Shapiro, et al.. (2003). Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia. The American Journal of Human Genetics. 72(2). 408–418. 487 indexed citations
9.
Dinulos, Mary Beth, et al.. (1999). Expansile bone lesions in a three-generation family. American Journal of Medical Genetics. 82(1). 1–5. 6 indexed citations
10.
Dinulos, Mary Beth & Roberta A Pagon. (1999). Autosomal dominant inheritance of Barber-Say syndrome. American Journal of Medical Genetics. 86(1). 54–56. 16 indexed citations
11.
Distèche, Christine M., Mary Beth Dinulos, Maria Teresa Bassi, Rosemary W. Elliott, & Elena I. Rugarli. (1998). Mapping of the murine Tbl1 gene reveals a new rearrangement between mouse and human X Chromosomes. Mammalian Genome. 9(12). 1062–1064. 15 indexed citations
12.
Eubanks, James H., Jayashree Srinivasan, Mary Beth Dinulos, Christine M. Distèche, & William A. Catterall. (1997). Structure and chromosomal localization of the β2 subunit of the human brain sodium channel. Neuroreport. 8(12). 2775–2779. 18 indexed citations
13.
Huq, A.H.M. Mahbubul, Rhonda S. Lovell, Margaret J. Sampson, et al.. (1996). Isolation, Mapping, and Functional Expression of the Mouse X Chromosome Glycerol Kinase Gene. Genomics. 36(3). 530–534. 19 indexed citations
14.
Saxena, Richa, Laura Brown, Trevor Hawkins, et al.. (1996). The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned. Nature Genetics. 14(3). 292–299. 355 indexed citations
15.
Lönberg, Nils, Mary Beth Dinulos, Christine M. Distèche, et al.. (1996). A Candidate Gene for theamnionlessGastrulation Stage Mouse Mutation Encodes a TRAF-Related Protein. Developmental Biology. 177(1). 274–290. 27 indexed citations
16.
Pera, Renee A. Reijo, Judith Seligman, Mary Beth Dinulos, et al.. (1996). Mouse Autosomal Homolog ofDAZ,a Candidate Male Sterility Gene in Humans, Is Expressed in Male Germ Cells before and after Puberty. Genomics. 35(2). 346–352. 116 indexed citations
17.
Matson, David O., Tamás Berke, Mary Beth Dinulos, et al.. (1996). Partial characterization of the genome of nine animal caliciviruses. Archives of Virology. 141(12). 2443–2456. 19 indexed citations
18.
Bressler, Steven L., Bryce L. Sopher, Qiongyi Hu, et al.. (1996). 786 Investigation of FE65 and its potential role in the etiology of Alzheimer's disease. Neurobiology of Aging. 17(4). S195–S195. 1 indexed citations
19.
Dinulos, Mary Beth, Maria Teresa Bassi, Elena I. Rugarli, et al.. (1996). A New Region of Conservation Is Defined between Human and Mouse X Chromosomes. Genomics. 35(1). 244–247. 15 indexed citations
20.
Dinulos, Mary Beth & David O. Matson. (1994). Recent developments with human caliciviruses. The Pediatric Infectious Disease Journal. 13(11). 998–1003. 12 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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