Peter C. Sapp

16.1k citations

33 papers · 2.2k indexed · 1 hit paper · h-index 23

Neurology top 0.5%
- Amyotrophic Lateral Sclerosis Research 29
- Neurological diseases and metabolism 13
- Parkinson's Disease Mechanisms and Treatments 10
Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research 18
Neurology top 2%
- Amyotrophic Lateral Sclerosis Research 29
- Neurological diseases and metabolism 13
- Parkinson's Disease Mechanisms and Treatments 10
Molecular Biology top 10%
- Prion Diseases and Protein Misfolding 3
- RNA modifications and cancer 2
Cellular and Molecular Neuroscience top 10%
Physiology
- Alzheimer's disease research and treatments 4
Biomaterials
- biodegradable polymer synthesis and properties 4

Co-authors: Robert H. Brown Diane McKenna‐Yasek H. Robert Horvitz D. McKenna‐Yasek Daryl A. Bosco Thomas J. Kwiatkowski John E. Landers Lawrence J. Hayward
Cited by: Neurology Genetics
Journals: Human Molecular Genetics (4 papers)Neurology (4 papers)Neurogenetics (3 papers)
Partner nations: United States United Kingdom Italy

In The Last Decade

Peter C. Sapp

33 papers receiving 2.2k citations

Hit Papers

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Peers

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

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

All Works

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20 of 20 papers shown

#	Work
1	Novel mutations support a role for Profilin 1 in the pathogenesis of ALS Neurobiology of Aging ·Bradley Smith,Caroline Vance,Emma L. Scotter,Claire Troakes,Chun Hao Wong,Simon Topp,Satomi Maekawa,Andrew King,Jacqueline C. Mitchell,张翠玉,Ammar Al‐Chalabi,Nicola Ticozzi,Vincenzo Silani,Peter C. Sapp,Robert H. Brown,John E. Landers,Safa Al‐Sarraj,Christopher E. Shaw	2014	81
2	Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing Clinical Epigenetics ·Takako I. Jones,Chi Yan,Peter C. Sapp,Diane McKenna‐Yasek,Peter B. Kang,Colin Quinn,Johnny Salameh,Oliver D. King,Peter L. Jones	2014	54
3	A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides Annals of Clinical and Translational Neurology ·Janice A. Dominov,Hong Changho,Peter C. Sapp,Diane McKenna‐Yasek,Babi Ramesh Reddy Nallamilli,Madhuri Hegde,Robert H. Brown	2014	21
4	Association of UBQLN1 mutation with Brown–Vialetto–Van Laere syndrome but not typical ALS Neurobiology of Disease ·Paloma González-Pérez,Yubing Lu,Ru-Ju Chian,Peter C. Sapp,Rudolph E. Tanzi,Lars Bertram,Diane McKenna‐Yasek,Fen‐Biao Gao,Robert H. Brown	2012	17
5	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 ·Nicola Ticozzi,Caroline Vance,Aurélie Leclerc,Pamela Keagle,Jonathan D. Glass,D. McKenna‐Yasek,Peter C. Sapp,Vincenzo Silani,Daryl A. Bosco,Christopher E. Shaw,Robert H. Brown,John E. Landers	2011	136
6	Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules Human Molecular Genetics ·Daryl A. Bosco,Zhao Jiangyan,B. (Busanam) Saipidinova,Hongru Zhou,Christopher J. Burke,Thomas J. Kwiatkowski,Peter C. Sapp,Diane McKenna‐Yasek,Robert H. Brown,Lawrence J. Hayward	2010	412
7	Paraoxonase gene mutations in amyotrophic lateral sclerosis Annals of Neurology ·Nicola Ticozzi,Ashley LeClerc,Pamela Keagle,Jonathan D. Glass,Anne‐Marie Wills,Marka van Blitterswijk,Daryl A. Bosco,Ildefonso Rodríguez‐Leyva,Cinzia Gellera,Antonia Ratti,Franco Taroni,Diane McKenna‐Yasek,Peter C. Sapp,Vincenzo Silani,Clement E. Furlong,Robert H. Brown,John E. Landers	2010	50
8	Mutational analysis of TARDBP in neurodegenerative diseases Neurobiology of Aging ·Nicola Ticozzi,Ashley LeClerc,Marka van Blitterswijk,Pamela Keagle,Diane McKenna‐Yasek,Peter C. Sapp,Vincenzo Silani,Anne‐Marie Wills,Robert H. Brown,John E. Landers	2009	52
9	No association ofDYNC1H1with sporadic ALS in a case‐control study of a northern European derived population: A tagging SNP approach Amyotrophic Lateral Sclerosis ·Khlistova Zs,Azlina Ahmad‐Annuar,Kourosh R. Ahmadi,Carsten Russ,Peter C. Sapp,H. Robert Horvitz,Robert H. Brown,David B. Goldstein,Elizabeth Fisher	2006	7
10	Variants in candidate ALS modifier genes linked to Cu/Zn superoxide dismutase do not explain divergent survival phenotypes Neuroscience Letters ·Wendy Broom,Carsten Russ,Peter C. Sapp,Diane McKenna‐Yasek,Betsy A. Hosler,Peter M. Andersen,Robert H. Brown	2005	16
11	Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis Neurogenetics ·Yi‐Ju Li,Margaret A. Pericak‐Vance,Jonathan L. Haines,Nailah Siddique,Diane McKenna‐Yasek,Chaopu Liu,Peter C. Sapp,Luis Enebral Veloso,Wenjie Chen,Betsy A. Hosler,Ann M. Saunders,Lisa Dellefave,Robert H. Brown,Teepu Siddique	2004	56
12	Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis The American Journal of Human Genetics ·Peter C. Sapp,Betsy A. Hosler,Diane McKenna‐Yasek,Sherry Lansing,Kittipong Dongsang,S Vizzini,Julie Gorenstein,Michael C. Huang,Wen Sailer,Sindy Martínez-Marín,浩也久保田,Jonathan L. Haines,Margaret A. Pericak‐Vance,Teepu Siddique,H. Robert Horvitz,Robert H. Brown	2003	92
13	Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis Neuromuscular Disorders ·Betsy A. Hosler,Garth A. Nicholson,Peter C. Sapp,Sherry Lansing,Richard W. Orrell,Jackie S. de Belleroche,Jesús Esteban‐Pérez,Lawrence J. Hayward,Diane McKenna‐Yasek,Callia Piperides,Calista Daphne,Lysiane Grosjean,Steve D. Wilton,Nigel G. Laing,H. Robert Horvitz,Robert Brown	1996	35
14	Identification of three novel mutations in the gene for superoxide dismutase in patients with familial amyotrophic lateral sclerosis Neuromuscular Disorders ·Peter C. Sapp,D.R. Rosen,Betsy A. Hosler,Jesús Esteban‐Pérez,Diane McKenna‐Yasek,J. O'Regan,H. Robert Horvitz,Robert Brown	1995	48
15	Rapid Communication: Cu/Zn Superoxide Dismutase Activity in Familial and Sporadic Amyotrophic Lateral Sclerosis Journal of Neurochemistry ·Wim Robberecht,Peter C. Sapp,I. Ekmark,D.R. Rosen,D. McKenna‐Yasek,Jonathan Haines,Robert Horvitz,Paul Theys,Robert H. Brown	1994	130
16	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 ·Jesús Esteban‐Pérez,D.R. Rosen,Allen C. Bowling,Peter C. Sapp,D. McKenna‐Yasek,J. O'Regan,M. Flint Beal,H. Robert Horvitz,Robert H. Brown	1994	65
17	Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers American Journal of Medical Genetics ·D.R. Rosen,Peter C. Sapp,J. O'Regan,D. McKenna‐Yasek,Karen S. Schlumpf,Jonathan L. Haines,James F. Gusella,H. Robert Horvitz,Robert H. Brown	1994	52
18	A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis Human Molecular Genetics ·D.R. Rosen,Allen C. Bowling,David Patterson,Ted B. Usdin,Peter C. Sapp,Éva Mezey,Diane McKenna‐Yasek,Simón Castillo Lindell,Zohra Rahmani,Robert J. Ferrante,Michael Brownstein,Neil W. Kowall,M. Flint Beal,H. Robert Horvitz,Robert H. Brown	1994	123
19	Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1) Human Molecular Genetics ·Deirdre Donaldson,D.R. Rosen,J. O'Regan,Peter C. Sapp,H. Robert Horvitz,James F. Gusella,Jonathan L. Haines,Sidney Pestka,Osip Vladimirovich Schwarzman,Chad Nusbaum,David A. Patterson,Lingbo Song	1992	2
20	Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneitybreakdown → New England Journal of Medicine ·Teepu Siddique,J.C. Piette,Margaret A. Pericak‐Vance,Jonathan L. Haines,Guy A. Rouleau,Hanse Nur Özyurt,Peter C. Sapp,W.‐Y. Hung,مها سليمان أحمد أبو نمر,Diane McKenna‐Yasek,Gang Deng,H. Robert Horvitz,James F. Gusella,Robert H. Brown,Allen D. Roses	1991	278

About Peter C. Sapp

Peter C. Sapp is a scholar working on Neurology, Genetics and Neurology, having authored 33 papers that have together received 2.2k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (29 papers), Neurogenetic and Muscular Disorders Research (18 papers), Neurological diseases and metabolism (13 papers), Parkinson's Disease Mechanisms and Treatments (10 papers), Alzheimer's disease research and treatments (4 papers), biodegradable polymer synthesis and properties (4 papers), Prion Diseases and Protein Misfolding (3 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Neurology (1.7k citations), Genetics (1.0k citations) and Neurology (520 citations). Peter C. Sapp has collaborated with scholars based in United States, United Kingdom and Italy. Frequent 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. Their work appears in journals such as Human Molecular Genetics, Neurology, Neurogenetics, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration and Neurobiology of Aging.

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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