Holly Dubbs

2.5k total citations
22 papers, 429 citations indexed

About

Holly Dubbs is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Holly Dubbs has authored 22 papers receiving a total of 429 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Holly Dubbs's work include Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (9 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Holly Dubbs is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (9 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Holly Dubbs collaborates with scholars based in United States, Italy and United Kingdom. Holly Dubbs's co-authors include Elaine H. Zackai, Surabhi Mulchandani, Laura K. Conlin, Nancy B. Spinner, Francisca Millan, Avni Santani, Addie I. Nesbitt, Kenneth N. Rosenbaum, Ann Nordgren and Helena Malmgren and has published in prestigious journals such as The American Journal of Human Genetics, JAMA Network Open and Genetics in Medicine.

In The Last Decade

Holly Dubbs

21 papers receiving 416 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Holly Dubbs United States 11 296 252 98 24 23 22 429
Mónica Rosello Spain 14 360 1.2× 295 1.2× 95 1.0× 22 0.9× 21 0.9× 41 535
Joanna Wiszniewska United States 12 360 1.2× 348 1.4× 106 1.1× 12 0.5× 28 1.2× 22 607
Aziza Sbiti Morocco 9 133 0.4× 211 0.8× 71 0.7× 12 0.5× 16 0.7× 19 387
Sanne M. C. Savelberg Netherlands 10 257 0.9× 246 1.0× 31 0.3× 38 1.6× 16 0.7× 11 443
Audrey Putoux France 11 215 0.7× 236 0.9× 72 0.7× 14 0.6× 8 0.3× 32 369
Siren Berland Norway 11 207 0.7× 360 1.4× 51 0.5× 8 0.3× 20 0.9× 28 478
Renske Oegema Netherlands 13 217 0.7× 245 1.0× 147 1.5× 23 1.0× 13 0.6× 21 534
Ender Karaca Türkiye 13 247 0.8× 265 1.1× 40 0.4× 8 0.3× 37 1.6× 25 544
Nicole Maas Belgium 7 351 1.2× 191 0.8× 101 1.0× 14 0.6× 12 0.5× 13 455
Rachel Sayuri Honjo Brazil 13 174 0.6× 205 0.8× 50 0.5× 10 0.4× 59 2.6× 60 460

Countries citing papers authored by Holly Dubbs

Since Specialization
Citations

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

Fields of papers citing papers by Holly Dubbs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Holly Dubbs

This figure shows the co-authorship network connecting the top 25 collaborators of Holly Dubbs. A scholar is included among the top collaborators of Holly Dubbs 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 Holly Dubbs. Holly Dubbs 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.
Iwata‐Otsubo, Aiko, Jorune Balciuniene, Cara Skraban, et al.. (2025). 16q24.3 Microdeletions Disrupting Upstream Non-Coding Region of ANKRD11 Cause KBG Syndrome. Genes. 16(2). 136–136. 1 indexed citations
2.
Nomakuchi, Tomoki, Dong Li, Holly Dubbs, et al.. (2024). Utility of genome sequencing in exome‐negative pediatric patients with neurodevelopmental phenotypes. American Journal of Medical Genetics Part A. 194(12). e63817–e63817.
3.
Dubbs, Holly, Xilma R. Ortiz‐González, & Eric D. Marsh. (2022). Pathogenic variants in CASK: Expanding the genotype–phenotype correlations. American Journal of Medical Genetics Part A. 188(9). 2617–2626. 7 indexed citations
4.
Gavazzi, Francesco, Samuel R. Pierce, Joseph Vithayathil, et al.. (2022). Psychometric outcome measures in beta-propeller protein-associated neurodegeneration (BPAN). Molecular Genetics and Metabolism. 137(1-2). 26–32. 7 indexed citations
5.
Cuddapah, Vishnu Anand, Holly Dubbs, Laura Adang, et al.. (2021). Understanding the phenotypic spectrum of ASXL‐related disease: Ten cases and a review of the literature. American Journal of Medical Genetics Part A. 185(6). 1700–1711. 18 indexed citations
6.
Clause, Amanda, Holly Dubbs, Denise Perry, et al.. (2021). Genome sequencing identifies three molecular diagnoses including a mosaic variant in the COL2A1 gene in an individual with Pol III–related leukodystrophy and Feingold syndrome. Molecular Case Studies. 7(6). a006143–a006143. 2 indexed citations
7.
Glass, Jennifer, Holly Dubbs, Margaret Harr, et al.. (2021). Trisomy 9 mosaic syndrome: Sixteen additional patients with new and/or less commonly reported features, literature review, and suggested clinical guidelines. American Journal of Medical Genetics Part A. 185(8). 2374–2383. 13 indexed citations
8.
Gavazzi, Francesco, Holly Dubbs, Valentina De Giorgis, et al.. (2020). Late-Onset Aicardi-Goutières Syndrome: A Characterization of Presenting Clinical Features. Pediatric Neurology. 115. 1–6. 17 indexed citations
9.
Beck, David B., T. Subramanian, S. Vijayalingam, et al.. (2019). A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity. Neurogenetics. 20(3). 129–143. 14 indexed citations
10.
Curiel, Julian, Steven J. Steinberg, Ann Snowden, et al.. (2017). X-linked adrenoleukodystrophy in a chimpanzee due to an ABCD1 mutation reported in multiple unrelated humans. Molecular Genetics and Metabolism. 122(3). 130–133. 4 indexed citations
11.
Samango‐Sprouse, Carole, et al.. (2017). 10‐year‐old female with intragenic KANSL1 mutation, no KANSL1‐related intellectual disability, and preserved verbal intelligence. American Journal of Medical Genetics Part A. 173(3). 762–765. 2 indexed citations
12.
Zárate, Yuri A., Louisa Kalsner, Alice Basinger, et al.. (2017). Genotype and phenotype in 12 additional individuals with SATB2‐associated syndrome. Clinical Genetics. 92(4). 423–429. 28 indexed citations
13.
Luo, Minjie, Jinbo Fan, Tara Wenger, et al.. (2017). CMIP haploinsufficiency in two patients with autism spectrum disorder and co‐occurring gastrointestinal issues. American Journal of Medical Genetics Part A. 173(8). 2101–2107. 5 indexed citations
14.
Tian, Guoling, Ana G. Cristancho, Holly Dubbs, et al.. (2016). A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of KIF 2A . Molecular Genetics & Genomic Medicine. 4(6). 599–603. 19 indexed citations
15.
Nesbitt, Addie I., Elizabeth Bhoj, Kristin McDonald Gibson, et al.. (2015). Exome sequencing expands the mechanism of SOX5‐associated intellectual disability: A case presentation with review of sox‐related disorders. American Journal of Medical Genetics Part A. 167(11). 2548–2554. 23 indexed citations
16.
Mulchandani, Surabhi, Elizabeth Bhoj, Minjie Luo, et al.. (2015). Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure. Genetics in Medicine. 18(4). 309–315. 73 indexed citations
17.
Kadhim, Muayad, Matthew A. Deardorff, Holly Dubbs, Elaine H. Zackai, & John P. Dormans. (2015). Melorheostosis. Journal of Pediatric Orthopaedics. 35(2). e13–e17. 5 indexed citations
18.
Tham, Emma, Anna Lindstrand, Avni Santani, et al.. (2015). Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features. The American Journal of Human Genetics. 96(3). 507–513. 87 indexed citations
19.
Luo, Minjie, Surabhi Mulchandani, Holly Dubbs, et al.. (2015). Detection of mutually exclusive mosaicism in a girl with genotype‐phenotype discrepancies. American Journal of Medical Genetics Part A. 167(12). 3091–3095. 5 indexed citations
20.
Kalish, Jennifer M., Laura K. Conlin, Tricia Bhatti, et al.. (2013). Clinical features of three girls with mosaic genome‐wide paternal uniparental isodisomy. American Journal of Medical Genetics Part A. 161(8). 1929–1939. 57 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

Breakdown of academic impact, for papers by Mónica Rosello Breakdown of academic impact, for papers by Joanna Wiszniewska Breakdown of academic impact, for papers by Aziza Sbiti Breakdown of academic impact, for papers by Sanne M. C. Savelberg Breakdown of academic impact, for papers by Audrey Putoux Breakdown of academic impact, for papers by Siren Berland Breakdown of academic impact, for papers by Renske Oegema Breakdown of academic impact, for papers by Ender Karaca Breakdown of academic impact, for papers by Nicole Maas Breakdown of academic impact, for papers by Rachel Sayuri Honjo
Rankless by CCL
2026