Sean Ennis

12.2k citations

61 papers · 2.5k indexed · 1 hit paper · h-index 27

Impact in

Neurology top 2%
- Amyotrophic Lateral Sclerosis Research
- Neurological diseases and metabolism
Genetics top 2%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases

Papers in

Genetics 27
- Genetics and Neurodevelopmental Disorders 9
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 6
- Genetic and phenotypic traits in livestock 4
Equine 1

Co-authors: T. F. Gallagher Andrew Green Orla Hardiman Sally Ann Lynch Judith Conroy Jochen H.M. Prehn Dairín Kieran Jillian P. Casey
Journals: European Journal of Human Genetics (5 papers)Scientific Reports (3 papers)Animal Genetics (3 papers)Neurology (2 papers)Epilepsia (2 papers)
Partner nations: Ireland United Kingdom United States

In The Last Decade

Sean Ennis

61 papers receiving 2.5k citations

Hit Papers

align trajectories log scale

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis 2006 · 518 citations

Peers

Countries citing papers authored by Sean Ennis

Since Specialization

Citations

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

Fields of papers citing papers by Sean Ennis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Sean Ennis, 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 Sean Ennis Line = papers co-authored together Sean Ennis links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Genetic Associations with Aging Muscle: A Systematic Review Cells ·Jedd Pratt, Colin Boreham, Sean Ennis, Anthony W. Ryan, Giuseppe De Vito	2019	56
2	A novel gain-of-function mutation in the ITPR1 suppressor domain causes spinocerebellar ataxia with altered Ca2+ signal patterns Journal of Neurology ·Jillian P. Casey, Wanda J. LaMar, Chihiro Hisatsune, Bryan Lynch, Raymond P. Murphy, Hazal IPEKCI, Akitoshi Miyamoto, Sean Ennis, Yoichi Paolo Shiga, C.O. Kim, Katsuhiko Mikoshiba, Sally Ann Lynch	2017	23
3	Novel European SLC1A4 variant: infantile spasms and population ancestry analysis Journal of Human Genetics ·Judith Conroy, Nicholas M. Allen, Kathleen M. Gorman, Balduzzi Alberto, Amre Shahwan, Bryan Lynch, Sally Ann Lynch, Sean Ennis, Mary D. King	2016	15
4	NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment Scientific Reports ·Jillian P. Casey, Svein I. Støve, Catherine McGorrian, Joseph Galvin, Kavita S. Hodgkins, Hazal IPEKCI, Sean Ennis, Francesca Brett, Mary D. King, Thomas Arnesen, Sally Ann Lynch	2015	56
5	A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder BMC Medical Genetics ·Jillian P. Casey, Patricia Goggin, Jennifer McDaid, Kinjal K Purohit, Sean Ennis, David R. Betts, Jane S. Lucas, B. Elnazir, Sally Ann Lynch	2015	10
6	Periventricular Calcification, Abnormal Pterins and Dry Thickened Skin: Expanding the Clinical Spectrum of RMND1? JIMD Reports ·Jillian P. Casey, Ellen Crushell, Kyle Thompson, Eilish Twomey, Langping He, Sean Ennis, Roy K. Philip, Robert W. Taylor, Mary D. King, Sally Ann Lynch	2015	5
7	Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci European Journal of Human Genetics ·Jia Shikong, Emma M. Quinn, Anthony W. Ryan, Judith Conroy, Valerie Trimble, Nasir Mahmud, Nicholas A. Kennedy, Aiden Corvin, Derek W. Morris, Gary Donohoe, Colm O’Morain, Padraic MacMathúna, Valerie Byrnes, Stavros Papaioannou, Gosia Trynka, Cisca Wijmenga, Dermot Kelleher, Sean Ennis, Richard Anney, Ross McManus	2015	27
8	TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural function Nature Genetics ·Fernando Gómez-Herreros, Janneke Schuurs-Hoeijmakers, Mark McCormack, Marie T. Greally, Stuart L. Rulten, Rocío Romero‐Granados, Timothy J. Counihan, Elijah Chaila, Judith Conroy, Sean Ennis, Norman Delanty, Felipe Cortés‐Ledesma, Arjan P.M. de Brouwer, Gianpiero L. Cavalleri, Sherif F. El‐Khamisy, Bert B.A. de Vries, Keith W. Caldecott	2014	115
9	Excellent outcome with de novo 15q13.3 microdeletion causing infantile spasms—A further patient American Journal of Medical Genetics Part A ·Nicholas M. Allen, Judith Conroy, Amre Shahwan, Sean Ennis, Bryan Lynch, Sally Ann Lynch, Mary D. King	2014	3
10	High-resolution Genome-wide Copy-number Analyses Identify Localized Copy-number Alterations in Ewing Sarcoma Diagnostic Molecular Pathology ·Miriam A. Lynn, Yuexiang Wang, Андрій Дєгтяр, Naisha Shah, Judith Conroy, Sean Ennis, T.J. Morris, David R. Betts, Jonathan A. Fletcher, Maureen J. O’Sullivan	2013	14
11	Recessive mutations in MCM4/PRKDC cause a novel syndrome involving a primary immunodeficiency and a disorder of DNA repair Journal of Medical Genetics ·Jillian P. Casey, Laila Azan, Paul McGettigan, Sally Ann Lynch, Sean Ennis	2012	38
12	First implication ofSTRA6mutations in isolated anophthalmia, microphthalmia, and coloboma: A new dimension to theSTRA6phenotype Human Mutation ·Jillian P. Casey, Riki Kawaguchi, M. A. Shampo, Hui Sun, Paul McGettigan, Jens Erik Nielsen, Judith Conroy, Regina Regan, Elaine Kenny, Paul Cormican, Derek W. Morris, Alex Priou, Muireann Ní Chróinín, Breandán N. Kennedy, Sally Ann Lynch, Andrew Green, Sean Ennis	2011	64
13	Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism Genes Brain & Behavior ·Catarina Correia, Ana Coutinho, Ana Filipa Sequeira, Inês Sousa, Emiro Rafael Buendía Dávila, J.-P. de Almeida, Cuaical Leiton, Blamires, Teresa S. Miguel, Jeffrey M. Conroy, Lynne Cochrane, Louise Gallagher, Michael Gill, Sean Ennis, Daniel McCollum, Astrid M. Vicente	2010	104
14	Agenesis of the corpus callosum with midline lipoma associated with an Xp22.31–Xp22.12 deletion Clinical Dysmorphology ·Lauren J. DePue, Judith Conroy, Veronica Donoghue, M. Mullarkey, Naisha Shah, Nuala Murphy, John Murphy, Sean Ennis, Sally Ann Lynch	2010	2
15	Late-onset central hypoventilation syndrome: a family genetic study European Respiratory Journal ·Liam Doherty, John Kiely, Paul Deegan, Marta Tesema Lalore, Tahsin Mehdi, Andrew Green, Sean Ennis, Walter T. McNicholas	2007	38
16	ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis Nature Genetics ·Matthew Greenway, Peter M. Andersen, Carsten Russ, Sean Ennis, Susan M. Cashman, Colette Donaghy, Victor Patterson, Robert Swingler, Dairín Kieran, Jochen H.M. Prehn, Karen Morrison, Andrew Green, K. Ravi Acharya, Robert H. Brown, Orla Hardiman Hit paper breakdown →	2006	518
17	Mutation analysis of the RET gene in total intestinal aganglionosis by wave DNA fragment analysis system Journal of Pediatric Surgery ·Valeria Solari, Sean Ennis, Akihiro Yoneda, Lai-Yee Wong, Antonio Messineo, M. Höllwarth, Andrew Green, Prem Puri	2003	14
18	Sry-negative XX sex reversal in a pony: a case report Theriogenology ·Laurence M. Vaughan, Choon Sheong Seow, Sean Ennis	2001	19
19	Cloning of the bovine activin receptor type II gene (ACVR2) and mapping to chromosome 2 (BTA2) Cytogenetic and Genome Research ·N. Flavin, Rémi Étienne, Luís V. Monteagudo, Sean Ennis, 岸上美智代, W. Barendse, María Victoria Arruga Laviña, Mark Rogers	1996	32
20	Fluorescent in situ localization of the bovine Activin receptor type IIA locus on Chromosome 2 (2q2.3-2.4) Mammalian Genome ·Luís V. Monteagudo, Rémi Étienne, N. Flavin, Mark Rogers, Sean Ennis, María Victoria Arruga Laviña	1996	1

About Sean Ennis

Sean Ennis is a scholar working on Genetics, Equine, Molecular Biology, Cell Biology and Transplantation, having authored 61 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (6 papers), Retinal Development and Disorders (5 papers), Congenital heart defects research (4 papers), Amyotrophic Lateral Sclerosis Research (4 papers), Cancer-related gene regulation (4 papers) and Genetic and phenotypic traits in livestock (4 papers). The work is most often cited by research in Neurology (591 citations), Genetics (394 citations), Genetics (782 citations), Neurology (204 citations) and Cellular and Molecular Neuroscience (331 citations). Sean Ennis has collaborated with scholars based in Ireland, United Kingdom and United States. Frequent co-authors include T. F. Gallagher, Andrew Green, Orla Hardiman, Sally Ann Lynch, Judith Conroy, Jochen H.M. Prehn, Dairín Kieran, Jillian P. Casey, Matthew Greenway and Robert H. Brown. Their work appears in journals such as European Journal of Human Genetics, Scientific Reports, Animal Genetics, Neurology and Epilepsia.

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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