Dan Doherty

9.5k total citations · 1 hit paper
73 papers, 3.5k citations indexed

About

Dan Doherty is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Dan Doherty has authored 73 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 39 papers in Genetics and 32 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Dan Doherty's work include Genetic and Kidney Cyst Diseases (30 papers), Fetal and Pediatric Neurological Disorders (29 papers) and Hedgehog Signaling Pathway Studies (18 papers). Dan Doherty is often cited by papers focused on Genetic and Kidney Cyst Diseases (30 papers), Fetal and Pediatric Neurological Disorders (29 papers) and Hedgehog Signaling Pathway Studies (18 papers). Dan Doherty collaborates with scholars based in United States, Netherlands and United Kingdom. Dan Doherty's co-authors include Ian A. Glass, Melissa A. Parisi, Kimberly A. Aldinger, Gisele E. Ishak, Ian G. Phelps, Diana R. O’Day, Jennifer C. Dempsey, Jay Shendure, Phillip F. Chance and A. James Barkovich and has published in prestigious journals such as Science, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Dan Doherty

72 papers receiving 3.5k 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.

A human cell atlas of fetal gene expression

2020 383 citations Junyue Cao, Diana R. O’Day et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dan Doherty United States	30	2.3k	1.7k	946	436	296	73	3.5k
A. Micheil Innes Canada	33	2.0k 0.9×	1.1k 0.6×	531 0.6×	325 0.7×	353 1.2×	113	3.5k
Chérif Beldjord France	30	2.5k 1.1×	1.3k 0.8×	453 0.5×	698 1.6×	686 2.3×	59	4.3k
Erica E. Davis United States	29	2.4k 1.0×	1.9k 1.1×	284 0.3×	548 1.3×	112 0.4×	68	3.1k
Tom Glaser United States	31	5.9k 2.6×	1.8k 1.0×	672 0.7×	637 1.5×	716 2.4×	51	7.7k
Yuanyi Feng United States	22	1.8k 0.8×	634 0.4×	305 0.3×	1.2k 2.7×	525 1.8×	34	3.1k
Pierre Billuart France	30	2.4k 1.0×	1.1k 0.6×	198 0.2×	769 1.8×	887 3.0×	63	3.8k
Shigemi Hayashi United States	11	3.2k 1.4×	832 0.5×	191 0.2×	384 0.9×	460 1.6×	12	4.1k
Matthew R. Sarkisian United States	32	1.7k 0.7×	780 0.5×	545 0.6×	397 0.9×	1.1k 3.7×	63	3.5k
Kerstin Kutsche Germany	32	2.3k 1.0×	1.3k 0.8×	198 0.2×	685 1.6×	358 1.2×	118	3.6k
Angelo Selicorni Italy	29	2.5k 1.1×	1.8k 1.1×	553 0.6×	168 0.4×	191 0.6×	176	3.8k

Countries citing papers authored by Dan Doherty

Since Specialization

Citations

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

Fields of papers citing papers by Dan Doherty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dan Doherty

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

All Works

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20 of 20 papers shown

MacDuffie, Katherine E., Jason L. Stein, Dan Doherty, et al.. (2023). Donor perspectives on informed consent and use of biospecimens for brain organoid research. Stem Cell Reports. 18(7). 1389–1393. 12 indexed citations

Shen, Minjie, Qiping Dong, Carissa L. Sirois, et al.. (2023). Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway. Nature Communications. 14(1). 3801–3801. 16 indexed citations

Doherty, Dan, et al.. (2023). Central sleep apnea in patients with pontine tegmental cap dysplasia treated with supplemental oxygen: a case report. Journal of Clinical Sleep Medicine. 19(4). 843–849. 1 indexed citations

Eldomery, Mohammad K., Lorraine Potocki, Dana Marafi, et al.. (2022). De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. American Journal of Medical Genetics Part A. 188(8). 2360–2366. 3 indexed citations

Weghe, Julie C. Van De, et al.. (2022). Systematic analysis of cilia characteristics and Hedgehog signaling in five immortal cell lines. PLoS ONE. 17(12). e0266433–e0266433. 10 indexed citations

Zárate, Yuri A., et al.. (2021). Genetic and phenotypic heterogeneity in KIAA0753‐related ciliopathies. American Journal of Medical Genetics Part A. 188(1). 104–115. 5 indexed citations

Wright, Jason N., Dennis Shaw, Gisele E. Ishak, Dan Doherty, & Francisco A. Perez. (2020). Cerebellar Watershed Injury in Children. American Journal of Neuroradiology. 41(5). 923–928. 4 indexed citations

Domcke, Silvia, Andrew J. Hill, Riza M. Daza, et al.. (2020). A human cell atlas of fetal chromatin accessibility. Science. 370(6518). 230 indexed citations

Cao, Junyue, Diana R. O’Day, Hannah A. Pliner, et al.. (2020). A human cell atlas of fetal gene expression. Science. 370(6518). 383 indexed citations breakdown →

10.

Muir, Alison M., Jennifer L. Cohen, Sarah E. Sheppard, et al.. (2020). Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities. The American Journal of Human Genetics. 106(5). 623–631. 19 indexed citations

11.

Brooks, Brian P., Wadih M. Zein, A. Thompson, et al.. (2018). Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center. Ophthalmology. 125(12). 1937–1952. 41 indexed citations

12.

Aldinger, Kimberly A., Jennifer C. Dempsey, Hannah M. Tully, et al.. (2018). Rhombencephalosynapsis: Fused cerebellum, confused geneticists. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(4). 432–439. 20 indexed citations

13.

Shi, Xiaoyu, Galo García, Julie C. Van De Weghe, et al.. (2017). Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome. Nature Cell Biology. 19(10). 1178–1188. 133 indexed citations

14.

Milev, Miroslav P., Megan E. Grout, Djenann Saint‐Dic, et al.. (2017). Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction. The American Journal of Human Genetics. 101(2). 291–299. 32 indexed citations

15.

Vilboux, Thierry, Dan Doherty, Ian A. Glass, et al.. (2017). Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center. Genetics in Medicine. 19(8). 875–882. 88 indexed citations

16.

Chapman, Teresa, Francisco A. Perez, Gisele E. Ishak, & Dan Doherty. (2016). Prenatal diagnosis of Chudley–McCullough syndrome. American Journal of Medical Genetics Part A. 170(9). 2426–2430. 4 indexed citations

17.

Tully, Hannah M., Tara Wenger, Walter A. Kukull, Dan Doherty, & William B. Dobyns. (2016). Anatomical configurations associated with posthemorrhagic hydrocephalus among premature infants with intraventricular hemorrhage. Neurosurgical FOCUS. 41(5). E5–E5. 5 indexed citations

18.

Bachmann‐Gagescu, Ruxandra, Ian G. Phelps, Jennifer C. Dempsey, et al.. (2015). KIAA0586is Mutated in Joubert Syndrome. Human Mutation. 36(9). 831–835. 52 indexed citations

19.

Oegema, Renske, Thomas D. Cushion, Ian G. Phelps, et al.. (2015). Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes. Human Molecular Genetics. 24(18). 5313–5325. 61 indexed citations

20.

Ishak, Gisele E., Jennifer C. Dempsey, Dennis Shaw, et al.. (2012). Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity. Brain. 135(5). 1370–1386. 94 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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