P. F. Chance

1.9k citations

28 papers · 1.1k indexed · h-index 21

Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders 14
- Genetic Neurodegenerative Diseases 6
Neurology top 5%
- Neurological diseases and metabolism 8
- Peripheral Neuropathies and Disorders 2
Neurology top 5%
- Neurological diseases and metabolism 8
- Peripheral Neuropathies and Disorders 2
Genetics top 10%
- Connective tissue disorders research 5
- Neurogenetic and Muscular Disorders Research 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
Cell Biology top 10%
Molecular Biology
- Ubiquitin and proteasome pathways 3

Co-authors: Thomas D. Bird M. William Lensch Craig L. Bennett Norisada Matsunami Hillary Lipe Bruce A. Rabin David R. Cornblath John W. Griffin
Cited by: Cellular and Molecular Neuroscience Neurology
Journals: Journal of Clinical Investigation (1 paper)Brain (1 paper)Neurology (11 papers)
Partner nations: United States United Kingdom France

In The Last Decade

P. F. Chance

28 papers receiving 1.1k citations

Peers

Countries citing papers authored by P. F. Chance

Since Specialization

Citations

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

Fields of papers citing papers by P. F. Chance

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P. F. Chance. 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 P. F. Chance. The network helps show where P. F. Chance may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy Journal of Medical Genetics ·Angela M. B. Collie,Megan Landsverk,Elizabeth K. Ruzzo,Heather C. Mefford,Karen Buysse,J. R. Adkins,Dana Knutzen,K. Barnett,Robert H. Brown,G. Parry,Sabrina W. Yum,David Simpson,Richard K. Olney,Patrick F. Chinnery,Evan E. Eichler,P. F. Chance,Mark Hannibal	2009	35
2	SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy Neurology ·Mark Hannibal,Elizabeth K. Ruzzo,Lauren Miller,Benjamin G Betz,Jillian G. Buchan,Dana Knutzen,K. Barnett,Megan Landsverk,Alexis Brice,Éric Leguern,H. Melanie Bedford,Bradford B. Worrall,S. Lovitt,Stanley H. Appel,E. Andermann,Thomas D. Bird,P. F. Chance	2009	40
3	Late-onset hereditary axonal neuropathies Neurology ·Craig L. Bennett,Victoria H. Lawson,Kiri L. Brickell,Kim L. Isaacs,William Seltzer,Hillary Lipe,Michael D. Weiss,G. T. Carter,Kevin M. Flanigan,P. F. Chance,Thomas D. Bird	2008	15
4	In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome Neurogenetics ·Alexander G. Bassuk,Y. Z. Chen,Sat Dev Batish,Narasimhan Nagan,Puneet Opal,P. F. Chance,Craig L. Bennett	2006	42
5	Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures Neurogenetics ·Craig L. Bennett,H. M. Huynh,P. F. Chance,Ian A. Glass,Sídney M. Gospe	2005	28
6	Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C Neurology ·V A Street,Craig L. Bennett,Jeff Goldy,Andrew J. Shirk,Kleopas A. Kleopa,B.L. Tempel,Hillary Lipe,S. S. Scherer,Thomas D. Bird,P. F. Chance	2003	136
7	A community survey establishing the prevalence rate of autistic disorder in adults with learning disability Psychiatric Bulletin ·C. Morgan,M. Roy,Acácia Maria Lourenço Francisco Nasr,P. F. Chance,M. Hand,T. J. J. Mlele,Ashok Roy	2002	41
8	A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4 ) localizes to a 500-kb interval on chromosome 9q34 Neurogenetics ·Ian P. Blair,Craig L. Bennett,Annette Abel,Bruce A. Rabin,John W. Griffin,Kenneth H. Fischbeck,David R. Cornblath,P. F. Chance	2000	29
9	Autosomal dominant juvenile amyotrophic lateral sclerosis Brain ·Bruce A. Rabin,John W. Griffin,Barbara J. Crain,Mena Scavina,P. F. Chance,David R. Cornblath	1999	79
10	Molecular evolution of the CMT1A-REP region: a human- and chimpanzee- specific repeat Molecular Biology and Evolution ·Marcel P. Keller,Beth Seifried,P. F. Chance	1999	20
11	Overview of Hereditary Neuropathy with Liability to Pressure Palsies Annals of the New York Academy of Sciences ·P. F. Chance	1999	40
12	Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25 Human Genetics ·Joan E. Pellegrino,Roberta Ann V. George,Jacquelyn Biegel,Martin R. Farlow,Kathy Gardner,Judy Caress,Mark J. Brown,Timothy R. Rebbeck,Thomas D. Bird,P. F. Chance	1997	38
13	Autosomal dominant transmission of Dejerine-Sottas disease (HMSN III) Neurology ·David R. Lynch,Hiroyuki Hara,Sabrina W. Yum,P. F. Chance,Steven S. Scherer,Sally J. Bird,K. H. Fischbeck	1997	2
14	Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17q Neurology ·Joan E. Pellegrino,Timothy R. Rebbeck,Mark J. Brown,Thomas D. Bird,P. F. Chance	1996	58
15	New connexin32 mutations associated with X-linked Charcot-Marie-Tooth disease Neurology ·L.J. Bone,Niklas Dahl,M. William Lensch,P. F. Chance,Thaddeus E. Kelly,E. Le Guern,S. Magi,Gordon Parry,Howard K. Shapiro,S. Wang,Kenneth H. Fischbeck	1995	61
16	Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies Neurology ·P. F. Chance,M. William Lensch,Hillary Lipe,R. H. Brown,Thomas D. Bird	1994	36
17	Charcot-Marie-Tooth Syndrome Archives of Neurology ·P. F. Chance,David Pleasure	1993	32
18	Analysis of the DNA duplication 17p11.2 in Charcot‐Marie‐Tooth neuropathy type 1 pedigrees Neurology ·P. F. Chance,Norisada Matsunami,M. William Lensch,Blumberg Bs,Thomas D. Bird	1992	54
19	Trisomy 17p associated with Charcot‐Marie‐Tooth neuropathy type 1A phenotype Neurology ·P. F. Chance,Thomas D. Bird,Norisada Matsunami,M. William Lensch,Arthur R. Brothman,Gerald M. Feldman	1992	74
20	Evidence for a dosage effect at the X-linked steroid sulfatase locus in human tissues. PubMed ·P. F. Chance,Stanley M. Gartler	1983	20

About P. F. Chance

P. F. Chance is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology, having authored 28 papers that have together received 1.1k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (14 papers), Neurological diseases and metabolism (8 papers), Genetic Neurodegenerative Diseases (6 papers), Connective tissue disorders research (5 papers), Neurogenetic and Muscular Disorders Research (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Ubiquitin and proteasome pathways (3 papers) and Peripheral Neuropathies and Disorders (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (608 citations), Neurology (258 citations) and Neurology (315 citations). P. F. Chance has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Thomas D. Bird, M. William Lensch, Craig L. Bennett, Norisada Matsunami, Hillary Lipe, Bruce A. Rabin, David R. Cornblath, John W. Griffin, David Pleasure and Joan E. Pellegrino. Their work appears in journals such as Journal of Clinical Investigation, Brain and 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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