Peter C. Sapp

16.1k total citations · 1 hit paper
33 papers, 2.2k citations indexed

About

Peter C. Sapp is a scholar working on Neurology, Genetics and Neurology. According to data from OpenAlex, Peter C. Sapp has authored 33 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Neurology, 18 papers in Genetics and 13 papers in Neurology. Recurrent topics in Peter C. Sapp's work include Amyotrophic Lateral Sclerosis Research (29 papers), Neurogenetic and Muscular Disorders Research (18 papers) and Neurological diseases and metabolism (13 papers). Peter C. Sapp is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (29 papers), Neurogenetic and Muscular Disorders Research (18 papers) and Neurological diseases and metabolism (13 papers). Peter C. Sapp collaborates with scholars based in United States, United Kingdom and Italy. Peter C. Sapp's co-authors include Robert H. Brown, Diane McKenna‐Yasek, H. Robert Horvitz, D. McKenna‐Yasek, Daryl A. Bosco, Thomas J. Kwiatkowski, John E. Landers, Lawrence J. Hayward, D.R. Rosen and Christopher J. Burke and has published in prestigious journals such as New England Journal of Medicine, Neurology and Annals of Neurology.

In The Last Decade

Peter C. Sapp

33 papers receiving 2.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneity

1991 278 citations Teepu Siddique, Margaret A. Pericak‐Vance et al. New England Journal of Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Peter C. Sapp United States	23	1.7k	1.0k	949	520	260	33	2.2k
Hristelina Ilieva United States	14	1.3k 0.7×	731 0.7×	1.0k 1.1×	373 0.7×	326 1.3×	24	2.2k
Xun Hu China	12	1.7k 1.0×	986 1.0×	1.1k 1.1×	393 0.8×	359 1.4×	21	2.3k
Diane McKenna‐Yasek United States	25	1.9k 1.1×	1.2k 1.2×	1.5k 1.6×	531 1.0×	386 1.5×	35	3.0k
Mercedes Prudencio United States	25	1.3k 0.7×	610 0.6×	918 1.0×	269 0.5×	432 1.7×	47	1.9k
D. McKenna‐Yasek United States	15	1.1k 0.6×	656 0.6×	517 0.5×	354 0.7×	169 0.7×	19	1.4k
Leslie I. Grad Canada	19	908 0.5×	442 0.4×	1.2k 1.3×	301 0.6×	316 1.2×	20	1.9k
Stephanie May United Kingdom	11	1.4k 0.8×	789 0.8×	1.2k 1.3×	228 0.4×	414 1.6×	21	2.2k
Lindsey R. Fischer United States	7	1.1k 0.6×	694 0.7×	599 0.6×	228 0.4×	179 0.7×	9	1.6k
Monica Castanedes‐Casey United States	21	1.3k 0.7×	534 0.5×	924 1.0×	329 0.6×	626 2.4×	30	2.0k
Faisal Fecto United States	13	984 0.6×	532 0.5×	669 0.7×	314 0.6×	238 0.9×	19	1.6k

Countries citing papers authored by Peter C. Sapp

Since Specialization

Citations

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

Fields of papers citing papers by Peter C. Sapp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter C. Sapp

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

All Works

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20 of 20 papers shown

Czell, David, Peter C. Sapp, Christoph Neuwirth, et al.. (2017). Further analysis of KIFAP3 gene in ALS patients from Switzerland and Sweden. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 18(3-4). 302–304. 5 indexed citations

González-Pérez, Paloma, Ute Woehlbier, Ru-Ju Chian, et al.. (2015). Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients. Gene. 566(2). 158–165. 58 indexed citations

Smith, Bradley, Caroline Vance, Emma L. Scotter, et al.. (2014). Novel mutations support a role for Profilin 1 in the pathogenesis of ALS. Neurobiology of Aging. 36(3). 1602.e17–1602.e27. 81 indexed citations

Dominov, Janice A., Peter C. Sapp, Diane McKenna‐Yasek, et al.. (2014). A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides. Annals of Clinical and Translational Neurology. 1(9). 703–720. 21 indexed citations

Jones, Takako I., Chi Yan, Peter C. Sapp, et al.. (2014). Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing. Clinical Epigenetics. 6(1). 23–23. 54 indexed citations

González-Pérez, Paloma, Yubing Lu, Ru-Ju Chian, et al.. (2012). Association of UBQLN1 mutation with Brown–Vialetto–Van Laere syndrome but not typical ALS. Neurobiology of Disease. 48(3). 391–398. 17 indexed citations

Ticozzi, Nicola, Caroline Vance, Aurélie Leclerc, et al.. (2011). Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(3). 285–290. 136 indexed citations

Bosco, Daryl A., Hongru Zhou, Christopher J. Burke, et al.. (2010). Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules. Human Molecular Genetics. 19(21). 4160–4175. 412 indexed citations

Ticozzi, Nicola, Ashley LeClerc, Pamela Keagle, et al.. (2010). Paraoxonase gene mutations in amyotrophic lateral sclerosis. Annals of Neurology. 68(1). 102–107. 50 indexed citations

10.

Ticozzi, Nicola, Ashley LeClerc, Marka van Blitterswijk, et al.. (2009). Mutational analysis of TARDBP in neurodegenerative diseases. Neurobiology of Aging. 32(11). 2096–2099. 52 indexed citations

11.

Ahmad‐Annuar, Azlina, Kourosh R. Ahmadi, Carsten Russ, et al.. (2006). No association ofDYNC1H1with sporadic ALS in a case‐control study of a northern European derived population: A tagging SNP approach. Amyotrophic Lateral Sclerosis. 7(1). 46–56. 7 indexed citations

12.

Broom, Wendy, Carsten Russ, Peter C. Sapp, et al.. (2005). Variants in candidate ALS modifier genes linked to Cu/Zn superoxide dismutase do not explain divergent survival phenotypes. Neuroscience Letters. 392(1-2). 52–57. 16 indexed citations

13.

Li, Yi‐Ju, Margaret A. Pericak‐Vance, Jonathan L. Haines, et al.. (2004). Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis. Neurogenetics. 5(4). 209–213. 56 indexed citations

14.

Sapp, Peter C., Betsy A. Hosler, Diane McKenna‐Yasek, et al.. (2003). Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis. The American Journal of Human Genetics. 73(2). 397–403. 92 indexed citations

15.

Sapp, Peter C., D.R. Rosen, Betsy A. Hosler, et al.. (1995). Identification of three novel mutations in the gene for superoxide dismutase in patients with familial amyotrophic lateral sclerosis. Neuromuscular Disorders. 5(5). 353–357. 48 indexed citations

16.

Esteban‐Pérez, Jesús, D.R. Rosen, Allen C. Bowling, et al.. (1994). Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosis. Human Molecular Genetics. 3(6). 997–998. 65 indexed citations

17.

Robberecht, Wim, Peter C. Sapp, D.R. Rosen, et al.. (1994). Rapid Communication: Cu/Zn Superoxide Dismutase Activity in Familial and Sporadic Amyotrophic Lateral Sclerosis. Journal of Neurochemistry. 62(1). 384–387. 130 indexed citations

18.

Rosen, D.R., Allen C. Bowling, David Patterson, et al.. (1994). A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis. Human Molecular Genetics. 3(6). 981–987. 123 indexed citations

19.

Donaldson, Deirdre, D.R. Rosen, J. O'Regan, et al.. (1992). Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1). Human Molecular Genetics. 1(8). 651–651. 2 indexed citations

20.

Siddique, Teepu, Margaret A. Pericak‐Vance, Jonathan L. Haines, et al.. (1991). Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneity. New England Journal of Medicine. 324(20). 1381–1384. 278 indexed citations breakdown →

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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