Dinah Clark

2.6k total citations
21 papers, 711 citations indexed

About

Dinah Clark is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Dinah Clark has authored 21 papers receiving a total of 711 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Dinah Clark's work include Genomics and Chromatin Dynamics (9 papers), Prenatal Screening and Diagnostics (5 papers) and Genetic Syndromes and Imprinting (4 papers). Dinah Clark is often cited by papers focused on Genomics and Chromatin Dynamics (9 papers), Prenatal Screening and Diagnostics (5 papers) and Genetic Syndromes and Imprinting (4 papers). Dinah Clark collaborates with scholars based in United States, Canada and Japan. Dinah Clark's co-authors include Ian D. Krantz, Matthew A. Deardorff, Laird G. Jackson, Maninder Kaur, Nancy B. Spinner, Antonie D. Kline, Håkon Håkonarson, Jinglan Liu, Masashige Bando and Hugo Vega and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS Biology.

In The Last Decade

Dinah Clark

20 papers receiving 700 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dinah Clark United States 15 495 250 97 73 57 21 711
Alisha Wilkens United States 13 239 0.5× 255 1.0× 61 0.6× 67 0.9× 104 1.8× 20 438
L Korniszewski Poland 12 274 0.6× 249 1.0× 85 0.9× 51 0.7× 28 0.5× 26 498
Janice C. Palumbos United States 8 245 0.5× 161 0.6× 32 0.3× 28 0.4× 56 1.0× 13 391
Michael J. Dixon United Kingdom 9 263 0.5× 172 0.7× 92 0.9× 24 0.3× 7 0.1× 11 461
Jiale Xiang China 9 172 0.3× 88 0.4× 85 0.9× 82 1.1× 20 0.4× 24 345
Paola Primignani Italy 14 223 0.5× 82 0.3× 104 1.1× 8 0.1× 110 1.9× 32 526
Prachi Kothiyal United States 7 171 0.3× 211 0.8× 28 0.3× 15 0.2× 51 0.9× 12 373
Melanie Babcock United States 10 333 0.7× 315 1.3× 19 0.2× 150 2.1× 55 1.0× 17 497
Ahmet Karagüzel Türkiye 11 236 0.5× 95 0.4× 222 2.3× 14 0.2× 62 1.1× 24 458

Countries citing papers authored by Dinah Clark

Since Specialization
Citations

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

Fields of papers citing papers by Dinah Clark

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dinah Clark

This figure shows the co-authorship network connecting the top 25 collaborators of Dinah Clark. A scholar is included among the top collaborators of Dinah Clark 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 Dinah Clark. Dinah Clark 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.
Dahl, Neera K., Michelle S. Bloom, Fouad T. Chebib, et al.. (2023). The Clinical Utility of Genetic Testing in the Diagnosis and Management of Adults with Chronic Kidney Disease. Journal of the American Society of Nephrology. 34(12). 2039–2050. 29 indexed citations
2.
Stein, Quinn, et al.. (2023). Isolated benign persistent proteinuria with novel association of CUBN (cubilin) variants. SHILAP Revista de lepidopterología. 11(6). e7502–e7502. 2 indexed citations
3.
Singh, Gurmukteshwar, Reginald Gohh, Dinah Clark, et al.. (2022). Vignette-Based Reflections to Inform Genetic Testing Policies in Living Kidney Donors. Genes. 13(4). 592–592. 6 indexed citations
4.
Clark, Dinah, et al.. (2021). Preimplantation Genetic Testing for Kidney Disease-Related Genes: A Laboratory’s Experience. American Journal of Nephrology. 52(8). 684–690. 10 indexed citations
5.
Francey, Lauren J., Maninder Kaur, Håkon Håkonarson, et al.. (2013). Novel COCH mutation in a family with autosomal dominant late onset sensorineural hearing impairment and tinnitus. American Journal of Otolaryngology. 34(3). 230–235. 28 indexed citations
6.
Francey, Lauren J., Ellen Tsai, Yaru Zhao, et al.. (2013). Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in Asian populations. American Journal of Medical Genetics Part A. 161(9). 2148–2157. 16 indexed citations
7.
Tsai, Ellen, Laura K. Conlin, Heidi L. Rehm, et al.. (2013). PECONPI: A novel software for uncovering pathogenic copy number variations in non‐syndromic sensorineural hearing loss and other genetically heterogeneous disorders. American Journal of Medical Genetics Part A. 161(9). 2134–2147. 5 indexed citations
8.
Deardorff, Matthew A., et al.. (2012). Investigation of autistic features among individuals with mild to moderate Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 158A(8). 1841–1847. 22 indexed citations
9.
Clark, Dinah, Ilana Sherer, Matthew A. Deardorff, et al.. (2012). Identification of a prenatal profile of Cornelia de Lange syndrome (CdLS): A review of 53 CdLS pregnancies. American Journal of Medical Genetics Part A. 158A(8). 1848–1856. 37 indexed citations
10.
Chatfield, Kathryn C., Jennifer Li, Dinah Clark, et al.. (2012). Congenital heart disease in Cornelia de Lange syndrome: Phenotype and genotype analysis. American Journal of Medical Genetics Part A. 158A(10). 2499–2505. 33 indexed citations
11.
Slavin, Thomas P., Noam Lazebnik, Dinah Clark, et al.. (2012). Germline mosaicism in Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 158A(6). 1481–1485. 23 indexed citations
12.
Conlin, Laura K., Maninder Kaur, Kosuke Izumi, et al.. (2012). Utility of SNP arrays in detecting, quantifying, and determining meiotic origin of tetrasomy 12p in blood from individuals with Pallister–Killian syndrome. American Journal of Medical Genetics Part A. 158A(12). 3046–3053. 36 indexed citations
13.
Sherer, Ilana, Matthew A. Deardorff, Dinah Clark, et al.. (2011). Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature. American Journal of Medical Genetics Part A. 155(12). 3007–3024. 46 indexed citations
14.
Francey, Lauren J., Laura K. Conlin, Dinah Clark, et al.. (2011). Genome‐wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. American Journal of Medical Genetics Part A. 158A(2). 298–308. 70 indexed citations
15.
Rohatgi, Sarika, Dinah Clark, Antonie D. Kline, et al.. (2010). Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey. American Journal of Medical Genetics Part A. 152A(7). 1641–1653. 56 indexed citations
16.
Lambert, Michele P., et al.. (2010). The incidence of thrombocytopenia in children with Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 155(1). 33–37. 10 indexed citations
17.
Liu, Jinglan, Zhe Zhang, Masashige Bando, et al.. (2010). Genome-wide DNA methylation analysis in cohesin mutant human cell lines. Nucleic Acids Research. 38(17). 5657–5671. 17 indexed citations
18.
Liu, Jinglan, Zhe Zhang, Masashige Bando, et al.. (2009). Transcriptional Dysregulation in NIPBL and Cohesin Mutant Human Cells. PLoS Biology. 7(5). e1000119–e1000119. 180 indexed citations
19.
Liu, Jinglan, Zhe Zhang, Matthew A. Deardorff, et al.. (2009). SMC1Aexpression and mechanism of pathogenicity in probands with X-Linked Cornelia de Lange syndrome. Human Mutation. 30(11). 1535–1542. 39 indexed citations
20.
Kamath, Binita M., Brian Thiel, Xiaowu Gai, et al.. (2008). SNP array mapping of chromosome 20p deletions: Genotypes, phenotypes, and copy number variation. Human Mutation. 30(3). 371–378. 46 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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Rankless by CCL
2026