Karin M. Dent

3.3k total citations · 1 hit paper
29 papers, 2.1k citations indexed

About

Karin M. Dent is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Karin M. Dent has authored 29 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Karin M. Dent's work include Genomics and Rare Diseases (11 papers), BRCA gene mutations in cancer (9 papers) and Family and Disability Support Research (4 papers). Karin M. Dent is often cited by papers focused on Genomics and Rare Diseases (11 papers), BRCA gene mutations in cancer (9 papers) and Family and Disability Support Research (4 papers). Karin M. Dent collaborates with scholars based in United States, Canada and Netherlands. Karin M. Dent's co-authors include Michael J. Bamshad, Holly K. Tabor, Jay Shendure, Sarah Ng, Paul Shannon, Abigail W. Bigham, Chad D. Huff, Ethylin Wang Jabs, Kati J. Buckingham and Choli Lee and has published in prestigious journals such as Nature Genetics, Biological Psychiatry and Clinical Cancer Research.

In The Last Decade

Karin M. Dent

26 papers receiving 2.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Exome sequencing identifies the cause of a mendelian disorder

2009 1.3k citations Sarah Ng, Kati J. Buckingham et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Karin M. Dent United States	15	1.1k	950	264	231	168	29	2.1k
Andrew D. Skol United States	23	948 0.9×	762 0.8×	154 0.6×	163 0.7×	108 0.6×	56	2.3k
Idan Menashe Israel	25	749 0.7×	747 0.8×	227 0.9×	229 1.0×	207 1.2×	88	2.5k
Vandana Shashi United States	27	1.3k 1.2×	1.4k 1.5×	133 0.5×	174 0.8×	79 0.5×	98	2.9k
Jack A. Kosmicki United States	13	1.3k 1.2×	1.4k 1.5×	215 0.8×	72 0.3×	71 0.4×	20	2.9k
Luis A. Pérez‐Jurado Spain	36	1.5k 1.3×	1.6k 1.7×	222 0.8×	248 1.1×	55 0.3×	105	3.5k
Hong Pan China	25	529 0.5×	1.1k 1.2×	288 1.1×	273 1.2×	54 0.3×	123	2.0k
Bregje W.M. van Bon Netherlands	19	1.7k 1.6×	1.3k 1.4×	185 0.7×	194 0.8×	52 0.3×	43	2.9k
Arvid Heiberg Norway	26	376 0.3×	671 0.7×	186 0.7×	291 1.3×	180 1.1×	80	1.9k
Jacob L. McCauley United States	26	954 0.9×	834 0.9×	104 0.4×	264 1.1×	155 0.9×	74	3.0k
Kimberly F. Doheny United States	28	1.3k 1.1×	1.8k 1.9×	305 1.2×	471 2.0×	68 0.4×	48	3.8k

Countries citing papers authored by Karin M. Dent

Since Specialization

Citations

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

Fields of papers citing papers by Karin M. Dent

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karin M. Dent

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

1.

Strati, Paolo, Dai Chihara, Jason R. Westin, et al.. (2025). A Phase I Trial of Evorpacept, Lenalidomide, and Rituximab for Patients with B-Cell Non-Hodgkin Lymphoma. Clinical Cancer Research. 31(19). 4079–4088.

2.

Dent, Karin M., et al.. (2023). Prenatal patient perceptions of receiving difficult news over the telephone. Journal of Genetic Counseling. 32(4). 857–869. 2 indexed citations

3.

Baty, Bonnie Jeanne, et al.. (2023). Defining orienting language in the genetic counseling process. Journal of Genetic Counseling. 32(3). 685–697.

4.

Stark, Louisa A., et al.. (2023). Exploring the impact of virtual SPIKES training on genetic counselors' confidence to deliver difficult news. Journal of Genetic Counseling. 32(6). 1266–1275.

5.

Assoum, Mirna, Ange‐Line Bruel, Melissa Crenshaw, et al.. (2020). NovelKIAA1033/WASHC4mutations in three patients with syndromic intellectual disability and a review of the literature. American Journal of Medical Genetics Part A. 182(4). 792–797. 10 indexed citations

6.

Dent, Karin M., et al.. (2018). Brief Report: Pediatrician Perspectives Regarding Genetic Evaluations of Children with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. 49(2). 794–808. 16 indexed citations

7.

Hobson, Wendy L., et al.. (2018). Training Methods for Delivering Difficult News in Genetic Counseling and Genetics Residency Training Programs. Journal of Genetic Counseling. 27(6). 1497–1505. 9 indexed citations

8.

Tabor, Holly K., Seema M. Jamal, Joon‐Ho Yu, et al.. (2016). My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings. Genetics in Medicine. 19(4). 467–475. 25 indexed citations

9.

Stevenson, David A., et al.. (2014). Goltz syndrome and PORCN mosaicism. International Journal of Dermatology. 53(12). 1481–1484. 8 indexed citations

10.

Jamal, Seema M., Joon‐Ho Yu, Jessica X. Chong, et al.. (2013). Practices and Policies of Clinical Exome Sequencing Providers: Analysis and Implications. American Journal of Medical Genetics Part A. 161(5). 935–950. 55 indexed citations

11.

Jamal, Seema M., Joon‐Ho Yu, Jessica X. Chong, et al.. (2013). Practices and Policies of Clinical Exome Sequencing Providers: Analysis and Implications. American Journal of Medical Genetics Part A. n/a–n/a. 2 indexed citations

12.

Tabor, Holly K., Tracy Brazg, Margaret J. McMillin, et al.. (2012). Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms. American Journal of Medical Genetics Part A. 158A(6). 1310–1319. 89 indexed citations

13.

Ng, Sarah, Kati J. Buckingham, Choli Lee, et al.. (2009). Exome sequencing identifies the cause of a mendelian disorder. Nature Genetics. 42(1). 30–35. 1303 indexed citations breakdown →

14.

Dent, Karin M. & John C. Carey. (2006). Breaking difficult news in a newborn setting: Down syndrome as a paradigm. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 142C(3). 173–179. 31 indexed citations

15.

Schneider, Katherine A., Anu Chittenden, Steven Joffe, et al.. (2006). Ethical Issues in Cancer Genetics: 1) Whose Information Is It?. Journal of Genetic Counseling. 15(6). 491–503. 11 indexed citations

16.

Dent, Karin M., Diane M. Dunn, Lynne M. Kerr, et al.. (2005). Improved molecular diagnosis of dystrophinopathies in an unselected clinical cohort. American Journal of Medical Genetics Part A. 134A(3). 295–298. 117 indexed citations

17.

Dent, Karin M., Aileen Kenneson, Janice C. Palumbos, et al.. (2004). Methodology of a multistate study of congenital hearing loss: Preliminary data from Utah newborn screening. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 125C(1). 28–34. 24 indexed citations

18.

Chen, Zhong, Aurelia Meloni‐Ehrig, Janice C. Palumbos, et al.. (2001). Pure trisomy 10p resulting from an extra ring chromosome: Characterization by methods of advanced molecular cytogenetics. American Journal of Medical Genetics. 102(4). 379–382. 14 indexed citations

19.

Flory, J.D., Stephen B. Manuck, R E Ferrell, et al.. (1999). Neuroticism is not associated with the serotonin transporter (5-HTTLPR) polymorphism. Molecular Psychiatry. 4(1). 93–96. 110 indexed citations

20.

Manuck, Stephen B., Janine D. Flory, Robert E. Ferrell, et al.. (1999). Aggression and anger-related traits associated with a polymorphism of the tryptophan hydroxylase gene. Biological Psychiatry. 45(5). 603–614. 207 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