Ian G. Phelps

3.6k total citations
18 papers, 742 citations indexed

About

Ian G. Phelps is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ian G. Phelps has authored 18 papers receiving a total of 742 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ian G. Phelps's work include Genetic and Kidney Cyst Diseases (11 papers), Fetal and Pediatric Neurological Disorders (8 papers) and Hedgehog Signaling Pathway Studies (5 papers). Ian G. Phelps is often cited by papers focused on Genetic and Kidney Cyst Diseases (11 papers), Fetal and Pediatric Neurological Disorders (8 papers) and Hedgehog Signaling Pathway Studies (5 papers). Ian G. Phelps collaborates with scholars based in United States, Switzerland and Canada. Ian G. Phelps's co-authors include Dan Doherty, Ruxandra Bachmann‐Gagescu, Jennifer C. Dempsey, Gisele E. Ishak, Cecilia B. Moens, Ian A. Glass, George Stearns, Brian A. Link, Susan E. Brockerhoff and A. Micheil Innes and has published in prestigious journals such as Journal of Biological Chemistry, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Ian G. Phelps

17 papers receiving 738 citations

Peers

Countries citing papers authored by Ian G. Phelps

Since Specialization

Citations

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

Fields of papers citing papers by Ian G. Phelps

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ian G. Phelps. 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 Ian G. Phelps. The network helps show where Ian G. Phelps may publish in the future.

Co-authorship network of co-authors of Ian G. Phelps

This figure shows the co-authorship network connecting the top 25 collaborators of Ian G. Phelps. A scholar is included among the top collaborators of Ian G. Phelps 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 Ian G. Phelps. Ian G. Phelps 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:

18 of 18 papers shown

#	Work	Indexed citations
1	Differentiation latency and dormancy signatures define fetal liver hematopoietic stem cells at single-cell resolution 2025 ·Cell Reports ·Takashi Ishida, (unknown), Adam Heck, Ian G. Phelps, Barbara Varnum‐Finney, (unknown), (unknown), (unknown), (unknown), (unknown), Dana L. Jackson, Colleen Delaney, Shahin Rafii, Irwin D. Bernstein, Kimberly A. Aldinger, Cole Trapnell, Hui Zhao, Brandon Hadland	0
2	Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center 2017 ·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, (unknown), Meghana Vemulapalli, James C. Mullikin, May Christine V. Malicdan, William A. Gahl, Meral Gunay‐Aygun	88
3	Interpreting the clinical significance of combined variants in multiple recessive disease genes: systematic investigation of Joubert syndrome yields little support for oligogenicity 2017 ·Genetics in Medicine ·Ian G. Phelps, Jennifer C. Dempsey, Megan E. Grout, Christine R. Isabella, Hannah M. Tully, Dan Doherty, Ruxandra Bachmann‐Gagescu	23
4	Abnormal glycosylation in Joubert syndrome type 10 2017 ·PubMed ·Megan Kane, Mariska Davids, Michelle Bond, David R. Adams, Megan E. Grout, Ian G. Phelps, Diana R. O’Day, Jennifer C. Dempsey, (unknown), Gretchen Golas, Gilbert Vézina, Meral Gunay‐Aygun, John A. Hanover, Dan Doherty, Miao He, May Christine V. Malicdan, William A. Gahl, Cornelius F. Boerkoel	11
5	Mortality in Joubert syndrome 2017 ·American Journal of Medical Genetics Part A ·Jennifer C. Dempsey, Ian G. Phelps, Ruxandra Bachmann‐Gagescu, Ian A. Glass, Hannah M. Tully, Dan Doherty	20
6	Recessive Inactivating Mutations in TBCK, Encoding a Rab GTPase-Activating Protein, Cause Severe Infantile Syndromic Encephalopathy 2016 ·The American Journal of Human Genetics ·Jessica X. Chong, Viviana Caputo, Ian G. Phelps, Lorenzo Stella, Lisa Worgan, Jennifer C. Dempsey, (unknown), Vincenzo Leuzzi, Richard Webster, Antonio Pizzuti, Colby T. Marvin, Gisele E. Ishak, Simone Ardern‐Holmes, (unknown), Michael J. Bamshad, Xilma R. Ortiz‐González, Marco Tartaglia, Maya Chopra, Dan Doherty	39
7	KIAA0586is Mutated in Joubert Syndrome 2015 ·Human Mutation ·Ruxandra Bachmann‐Gagescu, Ian G. Phelps, Jennifer C. Dempsey, (unknown), Gisele E. Ishak, Evan A. Boyle, Meredith Wilson, Charles Marques Lourenço, Mutluay Arslan, Jay Shendure, Dan Doherty	52
8	Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes 2015 ·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	61
9	Rapid identification and recovery of ENU-induced mutations with next-generation sequencing and Paired-End Low-Error analysis 2015 ·BMC Genomics ·Luyuan Pan, Arish N Shah, Ian G. Phelps, Dan Doherty, Eric A. Johnson, Cecilia B. Moens	28
10	The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking 2015 ·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	59
11	Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies 2015 ·Journal of Medical Genetics ·Markus Schueler, Jan Halbritter, Ian G. Phelps, Daniela A. Braun, Edgar A. Otto, Jonathan D. Porath, Heon Yung Gee, Jay Shendure, Brian J. O’Roak, Jennifer A. Lawson, Marwa M. Nabhan, Neveen A. Soliman, Dan Doherty, Friedhelm Hildebrandt	30
12	Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy 2014 ·The American Journal of Human Genetics ·Kimberly A. Aldinger, (unknown), 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	78
13	Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy 2014 ·The American Journal of Human Genetics ·Kimberly A. Aldinger, (unknown), 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	2
14	The Joubert Syndrome-associated Missense Mutation (V443D) in the Abelson-helper Integration Site 1 (AHI1) Protein Alters Its Localization and Protein-Protein Interactions 2013 ·Journal of Biological Chemistry ·Karina Tuz, (unknown), Oscar Juárez, (unknown), (unknown), Ian G. Phelps, Michelle R. Lennartz, Ian A. Glass, Dan Doherty, Russell J. Ferland	27
15	GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome 2012 ·The American Journal of Human Genetics ·Dan Doherty, Albert E. Chudley, Gail Coghlan, Gisele E. Ishak, A. Micheil Innes, Edmond G. Lemire, R. Curtis Rogers, Aizeddin A. Mhanni, Ian G. Phelps, Steven J.M. Jones, Shing H. Zhan, Anthony P. Fejes, Hashem Shahin, Moien Kanaan, Hatice Akay, Mustafa Tekin, Barbara L. Triggs‐Raine, Teresa Zelinski	2
16	GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome 2012 ·The American Journal of Human Genetics ·Dan Doherty, Albert E. Chudley, Gail Coghlan, Gisele E. Ishak, A. Micheil Innes, Edmond G. Lemire, R. Curtis Rogers, Aizeddin A. Mhanni, Ian G. Phelps, Steven J.M. Jones, Shing H. Zhan, Anthony P. Fejes, Hashem Shahin, Moien Kanaan, Hatice Akay, Mustafa Tekin, Barbara L. Triggs‐Raine, Teresa Zelinski	81
17	Genotype–phenotype correlation in CC2D2A-related Joubert syndrome reveals an association with ventriculomegaly and seizures 2012 ·Journal of Medical Genetics ·Ruxandra Bachmann‐Gagescu, Gisele E. Ishak, Jennifer C. Dempsey, Jonathan Adkins, Diana R. O’Day, Ian G. Phelps, Meral Gunay‐Aygun, Antonie D. Kline, Krzysztof Szczałuba, Loreto Martorell, Abdulrahman Alswaid, (unknown), Shashidhar Pai, Louise Izatt, Anne Ronan, Melissa A. Parisi, Heather C. Mefford, Ian A. Glass, Dan Doherty	50
18	The ciliopathy gene cc2d2a controls zebrafish photoreceptor outer segment development through a role in Rab8-dependent vesicle trafficking 2011 ·Human Molecular Genetics ·Ruxandra Bachmann‐Gagescu, Ian G. Phelps, George Stearns, Brian A. Link, Susan E. Brockerhoff, Cecilia B. Moens, Dan Doherty	91

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