Jennifer C. Schymick

9.3k total citations
15 papers, 1.4k citations indexed

About

Jennifer C. Schymick is a scholar working on Neurology, Genetics and Neurology. According to data from OpenAlex, Jennifer C. Schymick has authored 15 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Neurology, 10 papers in Genetics and 6 papers in Neurology. Recurrent topics in Jennifer C. Schymick's work include Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Neurological diseases and metabolism (6 papers). Jennifer C. Schymick is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (10 papers) and Neurological diseases and metabolism (6 papers). Jennifer C. Schymick collaborates with scholars based in United States, United Kingdom and Italy. Jennifer C. Schymick's co-authors include Bryan J. Traynor, Kevin Talbot, J. Raphael Gibbs, Dena Hernández, Sonja W. Scholz, Andrew Singleton, John Hardy, Mar Matarín, Hon‐Chung Fung and Angela Britton and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and The Lancet Neurology.

In The Last Decade

Jennifer C. Schymick

15 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Jennifer C. Schymick United States	13	1000	581	496	356	221	15	1.4k
Chiara F. Valori Germany	16	528 0.5×	566 1.0×	808 1.6×	284 0.8×	119 0.5×	21	1.4k
Kevin P. Kenna Ireland	15	1.3k 1.3×	700 1.2×	348 0.7×	368 1.0×	69 0.3×	21	1.5k
Serena Lattante Italy	23	1.2k 1.2×	764 1.3×	771 1.6×	422 1.2×	215 1.0×	54	1.8k
Lillian M. Daughrity United States	9	740 0.7×	432 0.7×	564 1.1×	129 0.4×	68 0.3×	12	1.1k
Paul W.J. van Vught Netherlands	14	732 0.7×	439 0.8×	395 0.8×	254 0.7×	40 0.2×	22	1.0k
Maria Mattheijssens Belgium	19	867 0.9×	230 0.4×	443 0.9×	521 1.5×	163 0.7×	27	1.5k
Charlotte Ridler United States	9	668 0.7×	424 0.7×	536 1.1×	112 0.3×	66 0.3×	68	1.1k
Nailah Siddique United States	14	525 0.5×	295 0.5×	383 0.8×	216 0.6×	45 0.2×	20	938
Barbara Castellotti Italy	25	670 0.7×	341 0.6×	987 2.0×	252 0.7×	305 1.4×	65	1.8k
Nicholas J. Maragakis United States	8	590 0.6×	434 0.7×	660 1.3×	90 0.3×	65 0.3×	11	1.1k

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

Schymick, Jennifer C., Tina M. Cowan, Maura Ruzhnikov, et al.. (2021). Variable clinical severity in TANGO2 deficiency: Case series and literature review. American Journal of Medical Genetics Part A. 188(2). 473–487. 17 indexed citations

Steffes, L.C., et al.. (2020). Three Infants with Pathogenic Variants in the ABCA3 Gene: Presentation, Treatment, and Clinical Course. The Journal of Pediatrics. 231. 278–283.e2. 4 indexed citations

Xi, Zhengrui, Lorne Zinman, Danielle Moreno, et al.. (2013). Hypermethylation of the CpG Island Near the G4C2 Repeat in ALS with a C9orf72 Expansion. The American Journal of Human Genetics. 92(6). 981–989. 201 indexed citations

Schymick, Jennifer C. & Bryan Traynor. (2012). Expanding the genetics of amyotrophic lateral sclerosis and frontotemporal dementia. Alzheimer s Research & Therapy. 4(4). 30–30. 6 indexed citations

Traynor, Bryan J., Michael A. Nalls, J. Raphael Gibbs, et al.. (2010). Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients. Proceedings of the National Academy of Sciences. 107(27). 12335–12338. 22 indexed citations

Laaksovirta, Hannu, Terhi Peuralinna, Jennifer C. Schymick, et al.. (2010). Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. The Lancet Neurology. 9(10). 978–985. 164 indexed citations

Chiò, Adriano, Andrea Calvo, Cristina Moglia, et al.. (2010). Amyotrophic Lateral Sclerosis–Frontotemporal Lobar Dementia in 3 Families With p.Ala382Thr TARDBP Mutations. Archives of Neurology. 67(8). 1002–9. 48 indexed citations

Sha, Qiuying, Zhaogong Zhang, Jennifer C. Schymick, Bryan J. Traynor, & Shuanglin Zhang. (2009). Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis. BMC Medical Genetics. 10(1). 86–86. 17 indexed citations

Bo, Roberto Del, Stefania Corti, Domenico Santoro, et al.. (2009). No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort. Neurobiology of Aging. 32(6). 1157–1158. 13 indexed citations

10.

Chiò, Adriano, Gabriella Restagno, Maura Brunetti, et al.. (2009). Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation. Neurobiology of Aging. 30(8). 1272–1275. 109 indexed citations

11.

Guerreiro, Rita, Jennifer C. Schymick, Cynthia Crews, et al.. (2008). TDP-43 Is Not a Common Cause of Sporadic Amyotrophic Lateral Sclerosis. PLoS ONE. 3(6). e2450–e2450. 60 indexed citations

12.

Schymick, Jennifer C., Kevin Talbot, & Bryan J. Traynor. (2007). Genetics of sporadic amyotrophic lateral sclerosis. Human Molecular Genetics. 16(R2). R233–R242. 126 indexed citations

13.

Schymick, Jennifer C., Sonja W. Scholz, Hon‐Chung Fung, et al.. (2007). Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. The Lancet Neurology. 6(4). 322–328. 153 indexed citations

14.

Cronin, Simon, S Berger, Jinhui Ding, et al.. (2007). A genome-wide association study of sporadic ALS in a homogenous Irish population. Human Molecular Genetics. 17(5). 768–774. 143 indexed citations

15.

Fung, Hon‐Chung, Sonja W. Scholz, Mar Matarín, et al.. (2006). Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. The Lancet Neurology. 5(11). 911–916. 284 indexed citations

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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