Ryan E. Lamont

2.4k citations

35 papers · 850 indexed · h-index 16

Impact in

Cell Biology top 10%
- Zebrafish Biomedical Research Applications
Molecular Biology
- RNA modifications and cancer
- RNA Research and Splicing
- Angiogenesis and VEGF in Cancer
- RNA and protein synthesis mechanisms
- Mitochondrial Function and Pathology
- Peroxisome Proliferator-Activated Receptors

Papers in ⓘ

Clinical Biochemistry 6
- Metabolism and Genetic Disorders 6
Genetics 13
- Genomics and Rare Diseases 8

Co-authors: Sarah J. Childs (8 shared papers)Jillian S. Parboosingh (21 shared papers)A. Micheil Innes (19 shared papers)François P. Bernier (16 shared papers)Teresa Zelinski (3 shared papers)Lennart Lögdberg (1 shared paper)Marion E. Reid (1 shared paper)Christopher Smith (3 shared papers)
Journals: The American Journal of Human Genetics (5 papers)European Journal of Human Genetics (3 papers)Developmental Dynamics (2 papers)Developmental Biology (2 papers)Clinical Genetics (2 papers)
Partner nations: Canada United States Germany

In The Last Decade

Ryan E. Lamont

33 papers receiving 836 citations

Peers

Countries citing papers authored by Ryan E. Lamont

Since Specialization

Citations

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

Fields of papers citing papers by Ryan E. Lamont

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ryan E. Lamont. 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 Ryan E. Lamont. The network helps show where Ryan E. Lamont may publish in the future.

Co-authors

The 25 scholars most cited alongside Ryan E. Lamont, 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 Ryan E. Lamont Line = papers co-authored together Ryan E. Lamont 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 35 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome The American Journal of Human Genetics ·Joy Armistead, Sunita Khatkar, Britta Meyer, Brian L. Mark, Nehal Patel, Gail Coghlan, Ryan E. Lamont, Shuangbo Liu, Jill Wiechert, Peter A. Cattini, P. Koetter, Klaus Wrogemann, Cheryl R. Greenberg, Karl‐Dieter Entian, Teresa Zelinski, Barbara L. Triggs‐Raine	2009	98
2	A Peroxisomal Disorder of Severe Intellectual Disability, Epilepsy, and Cataracts Due to Fatty Acyl-CoA Reductase 1 Deficiency The American Journal of Human Genetics ·Rebecca Buchert, Hasan Tawamie, Christopher Smith, Steffen Uebe, A. Micheil Innes, Bassam Al Hallak, Arif B. Ekici, Heinrich Sticht, Bernd Schwarze, Ryan E. Lamont, Jillian S. Parboosingh, François P. Bernier, Rami Abou Jamra	2014	95
3	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	78
4	The most common mutation inFKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations Human Mutation ·Patrick Frosk, Cheryl R. Greenberg, Alysa A.P. Tennese, Ryan E. Lamont, Edward Nylen, Cheryl Hirst, Danielle Frappier, Nicole M. Roslin, M Zaik, Kate Bushby, Volker Straub, Mayana Zatz, Flavia Paula, Kenneth Morgan, Takuya Fujiwara, Klaus Wrogemann	2004	53
5	PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes Life Science Alliance ·Tian Zhao, Caitlin Goedhart, Pingdewinde N. Sam, Rasha Sabouny, Susanne Lingrell, Adam J. Cornish, Ryan E. Lamont, François P. Bernier, David S. Sinasac, Jillian S. Parboosingh, Jean E. Vance, Steven M. Claypool, A. Micheil Innes, Timothy E. Shutt	2019	45
6	MAPping Out Arteries and Veins Science s STKE ·Ryan E. Lamont, Sarah J. Childs	2006	43
7	Human Blood Group Genes 2004: Chromosomal Locations and Cloning Strategies Transfusion Medicine Reviews ·Lennart Lögdberg, Marion E. Reid, Ryan E. Lamont, Teresa Zelinski	2005	42
8	Expansion of phenotype and genotypic data in CRB2-related syndrome European Journal of Human Genetics ·Ryan E. Lamont, Wen‐Hann Tan, A. Micheil Innes, Jillian S. Parboosingh, Dina Schneidman‐Duhovny, Aleksandar Rajkovic, John Pappas, Pablo Altschwager, Stephanie J. DeWard, Anne B. Fulton, Kathryn J. Gray, Max Krall, Lakshmi Mehta, Lance H. Rodan, Devereux N. Saller, Deanna Steele, Deborah R. Stein, Svetlana A. Yatsenko, François P. Bernier, Anne Slavotinek	2016	36
9	Hedgehog signaling via angiopoietin1 is required for developmental vascular stability Mechanisms of Development ·Ryan E. Lamont, Wendy T. Vu, Alyson D. Carter, Fabrizio C. Serluca, Calum A. MacRae, Sarah J. Childs	2010	35
10	Antagonistic interactions among Plexins regulate the timing of intersegmental vessel formation Developmental Biology ·Ryan E. Lamont, Erica J Lamont, Sarah J. Childs	2009	32
11	Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis European Journal of Human Genetics ·Tessa van Dijk, Sacha Ferdinandusse, Jos P.N. Ruiter, Mariëlle Alders, Inge B. Mathijssen, Jillian S. Parboosingh, A. Micheil Innes, Hanne Meijers-Heijboer, Bwee Tien Poll‐The, François P. Bernier, Ronald J. A. Wanders, Ryan E. Lamont, Frank Baas	2018	31
12	RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans The American Journal of Human Genetics ·Hanan E. Shamseldin, Anas M. Alazami, Melanie Manning, Amal Hashem, Oana Caluseiu, Brahim Tabarki, Edward D. Esplin, Susan Schelley, A. Micheil Innes, Jillian S. Parboosingh, Ryan E. Lamont, Jacek Majewski, François P. Bernier, Fowzan S. Alkuraya	2015	31
13	An Algorithm Measuring Donor Cell-Free DNA in Plasma of Cellular and Solid Organ Transplant Recipients That Does Not Require Donor or Recipient Genotyping Frontiers in Cardiovascular Medicine ·Paul M. K. Gordon, Anzalee Khan, Umair Sajid, Nicholas Chang, Varun Suresh, Leo S. Dimnik, Ryan E. Lamont, Jillian S. Parboosingh, Steven R. Martin, Richard T. Pon, Jene Weatherhead, Shelly Wegener, Debra Isaac, Steven C. Greenway	2016	26
14	Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies European Journal of Human Genetics ·Max Krall, Stephanie Htun, Rhonda E. Schnur, Alice S. Brooks, Laura Baker, Alejandra de Alba Campomanes, Ryan E. Lamont, Karen W. Gripp, Dina Schneidman‐Duhovny, A. Micheil Innes, Grazia M.S. Mancini, Anne Slavotinek	2019	26
15	Expression of multiple class three semaphorins in the retina and along the path of zebrafish retinal axons Developmental Dynamics ·Davon C. Callander, Ryan E. Lamont, Sarah J. Childs, Sarah McFarlane	2007	20
16	Biallelic CACNA2D2 variants in epileptic encephalopathy and cerebellar atrophy Annals of Clinical and Translational Neurology ·Jaya Punetha, Ender Karaca, Alper Gezdirici, Ryan E. Lamont, Davut Pehli̇van, Dana Marafi, Juan Pablo Appendino, Jill V. Hunter, Zeynep Coban‐Akdemir, Jawid M. Fatih, Shalini N. Jhangiani, Richard A. Gibbs, A. Micheil Innes, Jennifer E. Posey, James R. Lupski	2019	20
17	The LIM-homeodomain transcription factor Islet2a promotes angioblast migration Developmental Biology ·Ryan E. Lamont, Chang.-Yi. Wu, Jae Ryeon Ryu, Wendy T. Vu, Paniz Davari, Ryan E. Sobering, Regan M. Kennedy, Nicole Munsie, Sarah J. Childs	2016	14
18	Expansion of the GLE1‐associated arthrogryposis multiplex congenita clinical spectrum Clinical Genetics ·Christopher Smith, Jillian S. Parboosingh, Kym M. Boycott, C. Bönnemann, Jean K. Mah, Ryan E. Lamont, A. Micheil Innes, François P. Bernier	2016	14
19	Is PNPT1‐related hearing loss ever non‐syndromic? Whole exome sequencing of adult siblings expands the natural history of PNPT1‐related disorders American Journal of Medical Genetics Part A ·Alison Eaton, François P. Bernier, Caitlin Goedhart, Oana Caluseriu, Ryan E. Lamont, Kym M. Boycott, Jillian S. Parboosingh, A. Micheil Innes	2018	13
20	A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite population American Journal of Medical Genetics Part A ·Ryan E. Lamont, Chandree L. Beaulieu, François P. Bernier, Rebecca Sparkes, A. Micheil Innes, Candice Jackel‐Cram, Carole Ober, Jillian S. Parboosingh, Edmond G. Lemire	2016	13

About Ryan E. Lamont

Ryan E. Lamont is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Genetics and Transplantation, having authored 35 papers that have together received 850 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Metabolism and Genetic Disorders (6 papers), RNA modifications and cancer (6 papers), Angiogenesis and VEGF in Cancer (5 papers), Renal and related cancers (4 papers), Zebrafish Biomedical Research Applications (4 papers), Congenital heart defects research (4 papers) and Axon Guidance and Neuronal Signaling (4 papers). The work is most often cited by research in Cell Biology (148 citations), Molecular Biology (611 citations), Clinical Biochemistry (52 citations), Cellular and Molecular Neuroscience (133 citations) and Transplantation (19 citations). Ryan E. Lamont has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Sarah J. Childs, Jillian S. Parboosingh, A. Micheil Innes, François P. Bernier, Teresa Zelinski, Lennart Lögdberg, Marion E. Reid, Christopher Smith, Klaus Wrogemann and Cheryl R. Greenberg. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Developmental Dynamics, Developmental Biology and Clinical Genetics.

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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