Dan Doherty

9.7k citations

77 papers · 3.7k · 1 hit paper · h-index 32

Impact in

Genetics top 1%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
Pediatrics, Perinatology and Child Health top 0.5%
- Fetal and Pediatric Neurological Disorders

Papers in

Genetics 39
- Genetic and Kidney Cyst Diseases 30
- Genetics and Neurodevelopmental Disorders 7
- Genetic Syndromes and Imprinting 7
Molecular Biology 34
- Hedgehog Signaling Pathway Studies 15
- Congenital heart defects research 6

Co-authors: Ian A. Glass (16 shared papers)Melissa A. Parisi (10 shared papers)Kimberly A. Aldinger (6 shared papers)Gisele E. Ishak (15 shared papers)Ian G. Phelps (15 shared papers)Diana R. O’Day (7 shared papers)Jennifer C. Dempsey (18 shared papers)Jay Shendure (4 shared papers)
Journals: The American Journal of Human Genetics (10 papers)Journal of Medical Genetics (3 papers)Human Genetics and Genomics Advances (2 papers)Genetics in Medicine (2 papers)Neuropediatrics (2 papers)
Partner nations: United States United Kingdom Netherlands

In The Last Decade

Dan Doherty

75 papers receiving 3.6k citations

Dan Doherty's Hit Papers

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A human cell atlas of fetal gene expression 2020 · 410 citations

Peers

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-authors

The 25 scholars most cited alongside Dan Doherty, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Dan Doherty Line = papers co-authored together Dan Doherty links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 77 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A human cell atlas of fetal gene expression Science ·Junyue Cao, Diana R. O’Day, Hannah A. Pliner, Paul D. Kingsley, Mei Deng, Riza M. Daza, Michael Zager, Kimberly A. Aldinger, Ronnie Blecher‐Gonen, Fan Zhang, Malte Spielmann, James Palis, Dan Doherty, Frank J. Steemers, Ian A. Glass, Cole Trapnell, Jay Shendure Hit paper breakdown →	2020	410
2	Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome Nature Genetics ·Heleen H. Arts, Dan Doherty, Sylvia E. C. van Beersum, Melissa A. Parisi, Stef J.F. Letteboer, Nicholas T. Gorden, Theo Peters, Tina Märker, Krysta Voesenek, Aileen Kartono, Hamìt Özyürek, Federico M. Farin, Hester Y. Kroes, Uwe Wolfrum, Han G. Brunner, Frans P.M. Cremers, Ian A. Glass, Nine V.A.M. Knoers, Ronald Roepman	2007	247
3	A human cell atlas of fetal chromatin accessibility Science ·Silvia Domcke, Andrew J. Hill, Riza M. Daza, Junyue Cao, Diana R. O’Day, Hannah A. Pliner, Kimberly A. Aldinger, Dmitry Pokholok, Fan Zhang, Jennifer H. Milbank, Michael Zager, Ian A. Glass, Frank J. Steemers, Dan Doherty, Cole Trapnell, Darren A. Cusanovich, Jay Shendure	2020	245
4	Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability The American Journal of Human Genetics ·Muzammil Ahmad Khan, Muhammad Rafiq, Abdul Noor, Shobbir Hussain, Joana V. Flores, Verena Rupp, Akshita K. Vincent, Roland Malli, Ghazanfar Ali, Falak Sher Khan, Gisele E. Ishak, Dan Doherty, Rosanna Weksberg, Muhammad Ayub, Christian Windpassinger, Shahnaz Ibrahim, Michaela Frye, Muhammad Ansar, John B. Vincent	2012	193
5	Joubert syndrome (and related disorders) (OMIM 213300) European Journal of Human Genetics ·Melissa A. Parisi, Dan Doherty, Phillip F. Chance, Ian A. Glass	2007	163
6	OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin The American Journal of Human Genetics ·Karlien L. M. Coene, Ronald Roepman, Dan Doherty, Bushra Afroze, Hester Y. Kroes, Stef J.F. Letteboer, Lock Hock Ngu, Bartłomiej Budny, Erwin van Wijk, Nicholas T. Gorden, Malika Azhimi, Christel Thauvin‐Robinet, Joris A. Veltman, Mireille Boink, Tjitske Kleefstra, Frans P.M. Cremers, Hans van Bokhoven, Arjan P.M. de Brouwer	2009	145
7	Super-resolution microscopy reveals that disruption of ciliary transition-zone architecture causes Joubert syndrome Nature Cell Biology ·Xiaoyu Shi, Galo García, Julie C. Van De Weghe, Ryan McGorty, Gregory J. Pazour, Dan Doherty, Bo Huang, Jeremy F. Reiter	2017	137
8	Joubert Syndrome: Insights Into Brain Development, Cilium Biology, and Complex Disease Seminars in Pediatric Neurology ·Dan Doherty	2009	135
9	Hypomorphism for RPGRIP1L, a Ciliary Gene Vicinal to the FTO Locus, Causes Increased Adiposity in Mice Cell Metabolism ·George Stratigopoulos, Jayne F. Martin Carli, Diana R. O’Day, Liheng Wang, Charles A. LeDuc, Patricia Lanzano, Wendy K. Chung, Michael Rosenbaum, Dieter Egli, Dan Doherty, Rudolph L. Leibel	2014	131
10	Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity Brain ·Gisele E. Ishak, Jennifer C. Dempsey, Dennis Shaw, Hannah M. Tully, Margaret P Adam, Pedro A. Sanchez‐Lara, Ian A. Glass, Tessa Rue, Kathleen J. Millen, William B. Dobyns, Dan Doherty	2012	109
11	Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation The American Journal of Human Genetics ·Asif Mir, Liana Kaufman, Abdul Noor, M. Mahdi Motazacker, Talal Jamil, Matloob Azam, Kimia Kahrizi, Muhammad Rafiq, Rosanna Weksberg, Tanveer Nasr, Farooq Naeem, Andreas Tzschach, Andreas W. Kuß, Gisele E. Ishak, Dan Doherty, Hans‐Hilger Ropers, A. James Barkovich, Hossein Najmabadi, Muhammad Ayub, John B. Vincent	2009	101
12	The ciliopathy gene cc2d2a controls zebrafish photoreceptor outer segment development through a role in Rab8-dependent vesicle trafficking Human Molecular Genetics ·Ruxandra Bachmann‐Gagescu, Ian G. Phelps, George Stearns, Brian A. Link, Susan E. Brockerhoff, Cecilia B. Moens, Dan Doherty	2011	93
13	Midbrain and hindbrain malformations: advances in clinical diagnosis, imaging, and genetics The Lancet Neurology ·Dan Doherty, Kathleen J. Millen, A. James Barkovich	2013	92
14	Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center Genetics in Medicine ·Thierry Vilboux, Dan Doherty, Ian A. Glass, Melissa A. Parisi, Ian G. Phelps, Andrew R. Cullinane, Wadih M. Zein, Brian P. Brooks, Theo Heller, Ariane Soldatos, Neal L. Oden, Deniz Yildirimli, Meghana Vemulapalli, James C. Mullikin, May Christine V. Malicdan, William A. Gahl, Meral Gunay‐Aygun	2017	91
15	Disruption to control network function correlates with altered dynamic connectivity in the wider autism spectrum NeuroImage Clinical ·Nina de Lacy, Dan Doherty, Brian King, Srinivas Rachakonda, Vince D. Calhoun	2017	87
16	Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy The American Journal of Human Genetics ·Kimberly A. Aldinger, Stephen J. Mosca, Martine Tétreault, Jennifer C. Dempsey, Gisele E. Ishak, Taila Hartley, Ian G. Phelps, Ryan E. Lamont, Diana R. O’Day, Donald Basel, Karen W. Gripp, Laura Baker, Mark J. Stephan, François P. Bernier, Kym M. Boycott, Jacek Majewski, Jillian S. Parboosingh, A. Micheil Innes, Dan Doherty	2014	85
17	Joubert syndrome: brain and spinal cord malformations in genotyped cases and implications for neurodevelopmental functions of primary cilia Acta Neuropathologica ·Gordana Juric‐Sekhar, Jonathan Adkins, Dan Doherty, Robert F. Hevner	2012	72
18	Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes Human Molecular Genetics ·Renske Oegema, Thomas D. Cushion, Ian G. Phelps, Seo‐Kyung Chung, Jennifer C. Dempsey, Sarah Collins, Jonathan G.L. Mullins, Tracy Dudding, Harinder Gill, Andrew Green, William B. Dobyns, Gisele E. Ishak, Mark I. Rees, Dan Doherty	2015	64
19	Pontine Tegmental Cap Dysplasia: MR Imaging and Diffusion Tensor Imaging Features of Impaired Axonal Navigation American Journal of Neuroradiology ·Patrice Jissendi‐Tchofo, Dan Doherty, George McGillivray, Robert F. Hevner, Dennis Shaw, Gisele E. Ishak, Richard J. Leventer, A. James Barkovich	2008	63
20	The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking PLoS Genetics ·Ruxandra Bachmann‐Gagescu, Margo Dona, Lisette Hetterschijt, E.L.G.M. Tonnaer, Theo Peters, Erik de Vrieze, Dorus A. Mans, Sylvia E. C. van Beersum, Ian G. Phelps, Heleen H. Arts, Jan E.E. Keunen, Marius Ueffing, Ronald Roepman, Karsten Boldt, Dan Doherty, Cecilia B. Moens, Stephan C. F. Neuhauss, Hannie Kremer, Erwin van Wijk	2015	59

About Dan Doherty

Dan Doherty is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Cell Biology, having authored 77 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (30 papers), Fetal and Pediatric Neurological Disorders (25 papers), Hedgehog Signaling Pathway Studies (15 papers), Neonatal and fetal brain pathology (7 papers), Prenatal Screening and Diagnostics (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genetic Syndromes and Imprinting (7 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Genetics (1.7k citations), Pediatrics, Perinatology and Child Health (863 citations), Molecular Biology (2.1k citations), Cell Biology (422 citations) and Biophysics (110 citations). Dan Doherty has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent 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 Kathleen J. Millen. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics, Human Genetics and Genomics Advances, Genetics in Medicine and Neuropediatrics.

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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