Jennifer C. Schymick

9.3k citations

15 papers · 1.4k indexed · h-index 13

Co-authors: Bryan J. Traynor Kevin Talbot J. Raphael Gibbs Dena Hernández Sonja W. Scholz Andrew Singleton John Hardy Mar Matarín
Topics: Amyotrophic Lateral Sclerosis Research (12 papers)Neurogenetic and Muscular Disorders Research (10 papers)Neurological diseases and metabolism (6 papers)
Cited by: Neurology Genetics
Journals: Proceedings of the National Academy of Sciences PLoS ONE The Lancet Neurology
Partner nations: United States United Kingdom Italy

In The Last Decade

Jennifer C. Schymick

15 papers receiving 1.3k citations

Peers

Countries citing papers authored by Jennifer C. Schymick

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer C. Schymick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jennifer C. Schymick. 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 Jennifer C. Schymick. The network helps show where Jennifer C. Schymick may publish in the future.

Co-authorship network of co-authors of Jennifer C. Schymick

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Variable clinical severity in TANGO2 deficiency: Case series and literature review 2021 ·American Journal of Medical Genetics Part A ·Jennifer C. Schymick,(unknown),Tina M. Cowan,Maura Ruzhnikov,(unknown),Liliana Fernández,(unknown),(unknown),Vamsi V. Yarlagadda,Matthew T. Wheeler,Jonathan A. Bernstein,Gregory M. Enns,Chung Lee	17
2	Three Infants with Pathogenic Variants in the ABCA3 Gene: Presentation, Treatment, and Clinical Course 2020 ·The Journal of Pediatrics ·(unknown),L.C. Steffes,Jennifer C. Schymick,Florette K. Hazard,Michael C. Tracy,David N. Cornfield	4
3	Hypermethylation of the CpG Island Near the G4C2 Repeat in ALS with a C9orf72 Expansion 2013 ·The American Journal of Human Genetics ·Zhengrui Xi,Lorne Zinman,Danielle Moreno,Jennifer C. Schymick,Yan Liang,Christine Sato,Yonglan Zheng,Mahdi Ghani,Samar Dib,Julia Keith,Janice Robertson,Ekaterina Rogaeva	201
4	Expanding the genetics of amyotrophic lateral sclerosis and frontotemporal dementia 2012 ·Alzheimer s Research & Therapy ·Jennifer C. Schymick,Bryan Traynor	6
5	Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients 2010 ·Proceedings of the National Academy of Sciences ·Bryan J. Traynor,Michael A. Nalls,(unknown),J. Raphael Gibbs,Jennifer C. Schymick,Sampath Arepalli,Dena Hernandez,Marcel P. van der Brug,Janel O. Johnson,Allissa Dillman,Mark Cookson,Cristina Moglia,Andrea Calvo,Gabriella Restagno,Gabriele Mora,Adriano Chiò	22
6	Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study 2010 ·The Lancet Neurology ·Hannu Laaksovirta,Terhi Peuralinna,Jennifer C. Schymick,Sonja W. Scholz,(unknown),Liisa Myllykangas,Raimo Sulkava,Lilja Jansson,Dena Hernández,J. Raphael Gibbs,Michael A. Nalls,David Heckerman,Pentti J. Tienari,Bryan J. Traynor	164
7	Amyotrophic Lateral Sclerosis–Frontotemporal Lobar Dementia in 3 Families With p.Ala382Thr TARDBP Mutations 2010 ·Archives of Neurology ·Adriano Chiò,Andrea Calvo,Cristina Moglia,(unknown),(unknown),(unknown),Anna Montuschi,Angelina Cistaro,Anna Ticca,Bryan J. Traynor,Jennifer C. Schymick,Roberto Mutani,Maria Giovanna Marrosu,(unknown),Giuseppe Borghero	48
8	Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis 2009 ·BMC Medical Genetics ·Qiuying Sha,Zhaogong Zhang,Jennifer C. Schymick,Bryan J. Traynor,Shuanglin Zhang	17
9	No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort 2009 ·Neurobiology of Aging ·Roberto Del Bo,Stefania Corti,Domenico Santoro,(unknown),Chiara Fenoglio,Serena Ghezzi,Michela Ranieri,Daniela Galimberti,Michelangelo Mancuso,Gabriele Siciliano,Chiara Briani,Luigi Murri,Elio Scarpini,Jennifer C. Schymick,Bryan J. Traynor,Nereo Bresolin,Giacomo P. Comi	13
10	Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation 2009 ·Neurobiology of Aging ·Adriano Chiò,Gabriella Restagno,Maura Brunetti,Irene Ossola,Andrea Calvo,Gabriele Mora,Mario Sabatelli,Maria Rosaria Monsurrò,Stefania Battistini,Jessica Mandrioli,Fabrizio Salvi,Rossella Spataro,Jennifer C. Schymick,Bryan J. Traynor,Vincenzo La Bella	109
11	TDP-43 Is Not a Common Cause of Sporadic Amyotrophic Lateral Sclerosis 2008 ·PLoS ONE ·Rita Guerreiro,Jennifer C. Schymick,Cynthia Crews,Andrew Singleton,John Hardy,Bryan J. Traynor	60
12	Genetics of sporadic amyotrophic lateral sclerosis 2007 ·Human Molecular Genetics ·Jennifer C. Schymick,Kevin Talbot,Bryan J. Traynor	126
13	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data 2007 ·The Lancet Neurology ·Jennifer C. Schymick,Sonja W. Scholz,Hon‐Chung Fung,Angela Britton,Sampath Arepalli,J. Raphael Gibbs,Federica Lombardo,Mar Matarín,Dalia Kasperavičiūtė,Dena Hernández,Cynthia Crews,Lucie Bruijn,Jeffrey D. Rothstein,Gabriele Mora,Gabriella Restagno,Adriano Chiò,Andrew Singleton,John Hardy,Bryan J. Traynor	153
14	A genome-wide association study of sporadic ALS in a homogenous Irish population 2007 ·Human Molecular Genetics ·Simon Cronin,S Berger,Jinhui Ding,Jennifer C. Schymick,Nicole Washecka,D. G. Hernandez,M. J. Greenway,Daniel G. Bradley,Bryan J. Traynor,Orla Hardiman	143
15	Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data 2006 ·The Lancet Neurology ·Hon‐Chung Fung,Sonja W. Scholz,Mar Matarín,Javier Simón‐Sánchez,Dena Hernández,Angela Britton,J. Raphael Gibbs,Carl D. Langefeld,(unknown),Jennifer C. Schymick,Michael S. Okun,Ronald J. Mandel,Hubert H. Fernandez,Kelly D. Foote,Ramon L. Rodriguez,Elizabeth Peckham,Fabienne Wavrant De Vrieze,Katrina Gwinn,John Hardy,Andrew Singleton	284

About Jennifer C. Schymick

Jennifer C. Schymick is a scholar working on Genetics, Neurology and Neurology, having authored 15 papers that have together received 1.4k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Neurological diseases and metabolism (6 papers). The work is most often cited by research in Neurology (1000 citations), Genetics (581 citations) and Neurology (356 citations). Jennifer C. Schymick has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include Bryan J. Traynor, Kevin Talbot, J. Raphael Gibbs, Dena Hernández, Sonja W. Scholz, Andrew Singleton, John Hardy, Mar Matarín, Angela Britton and Hon‐Chung Fung. Their work appears in journals such as Proceedings of the National Academy of Sciences, PLoS ONE and The Lancet Neurology.

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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