Jeffrey M. Stajich

4.1k citations

41 papers · 1.7k indexed · h-index 20

Cellular and Molecular Neuroscience top 2%
Neurology top 2%
Molecular Biology
Neurology top 5%
Genetics top 10%

Co-authors: Jeffery M. Vance B.L. Scott William K. Scott Eden R. Martin Mark Stacy Margaret A. Pericak‐Vance Dana B. Hancock Larry H. Yamaoka
Topics: Muscle Physiology and Disorders (10 papers)Genetic Neurodegenerative Diseases (10 papers)Parkinson's Disease Mechanisms and Treatments (8 papers)
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: Nucleic Acids Research PLoS ONE Neurology
Partner nations: United States Netherlands Australia

In The Last Decade

Jeffrey M. Stajich

41 papers receiving 1.6k citations

Peers

Countries citing papers authored by Jeffrey M. Stajich

Since Specialization

Citations

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

Fields of papers citing papers by Jeffrey M. Stajich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeffrey M. Stajich. 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 Jeffrey M. Stajich. The network helps show where Jeffrey M. Stajich may publish in the future.

Co-authorship network of co-authors of Jeffrey M. Stajich

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffrey M. Stajich. A scholar is included among the top collaborators of Jeffrey M. Stajich 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 Jeffrey M. Stajich. Jeffrey M. Stajich 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

#	Work	Indexed citations
1	Stratified Whole Genome Linkage Analysis of Chiari Type I Malformation Implicates Known Klippel-Feil Syndrome Genes as Putative Disease Candidates 2013 ·PLoS ONE ·Christina A. Markunas,Karen Soldano,Kaitlyn Dunlap,Heidi Cope,(unknown),Jeffrey M. Stajich,David S. Enterline,Gerald A. Grant,Herbert E. Fuchs,Simon G. Gregory,Allison E. Ashley‐Koch	37
2	Exome Analysis of Two Limb-Girdle Muscular Dystrophy Families: Mutations Identified and Challenges Encountered 2012 ·PLoS ONE ·Kristin McDonald Gibson,Jeffrey M. Stajich,Colette Blach,Allison E. Ashley‐Koch,Michael A. Hauser	13
3	Genome‐Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease 2010 ·Annals of Human Genetics ·Todd L. Edwards,William K. Scott,(unknown),Amber Burt,Eric Powell,Gary W. Beecham,Liyong Wang,Stephan Züchner,Ioanna Konidari,Gaofeng Wang,Carlos Singer,Fatta B. Nahab,B.L. Scott,Jeffrey M. Stajich,Margaret A. Pericak‐Vance,Jonathan L. Haines,Jeffery M. Vance,Eden R. Martin	370
4	Native American myopathy: Congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia 2008 ·American Journal of Medical Genetics Part A ·Demetra S. Stamm,Arthur S. Aylsworth,Jeffrey M. Stajich,Stephen G. Kahler,Leigh B. Thorne,Marcy C. Speer,Cynthia M. Powell	50
5	Pesticide exposure and risk of Parkinson's disease: A family-based case-control study 2008 ·BMC Neurology ·Dana B. Hancock,Eden R. Martin,Gregory M. Mayhew,Jeffrey M. Stajich,(unknown),Mark Stacy,B.L. Scott,Jeffery M. Vance,William K. Scott	215
6	Smoking, Caffeine, and Nonsteroidal Anti-inflammatory Drugs in Families With Parkinson Disease 2007 ·Archives of Neurology ·Dana B. Hancock,Eden R. Martin,Jeffrey M. Stajich,(unknown),Mark Stacy,B.L. Scott,Jeffery M. Vance,William K. Scott	85
7	The genes encoding for D4Z4 binding proteins HMGB2, YY1, NCL, and MYOD1 are excluded as candidate genes for FSHD1B 2005 ·Neuromuscular Disorders ·(unknown),Jeffrey M. Stajich,Marcy C. Speer,John R. Gilbert	5
8	Fibroblast Growth Factor 20 Polymorphisms and Haplotypes Strongly Influence Risk of Parkinson Disease 2004 ·The American Journal of Human Genetics ·Joelle M. van der Walt,Maher Noureddine,Raja Kittappa,Michael A. Hauser,William K. Scott,Ron McKay,Fengyu Zhang,Jeffrey M. Stajich,Kenichiro Fujiwara,B.L. Scott,Margaret A. Pericak‐Vance,Jeffery M. Vance,Eden R. Martin	106
9	Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432 2002 ·Neurogenetics ·Marcy C. Speer,Felicia L. Graham,(unknown),(unknown),Jeffrey M. Stajich,P. C. Gaskell,Margaret A Pericak‐Vance,Jeffery M. Vance	7
10	Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy 2001 ·Journal of Clinical Neuromuscular Disease ·Richard W. Tim,John R. Gilbert,Jeffrey M. Stajich,(unknown),Kristi D. Viles,Rabi Tawil,George W. Padberg,Rune R. Frants,(unknown),Edward H. Bossen,Allan H. Friedman,Margaret A. Pericak‐Vance,Marcy C. Speer	7
11	Coexistence of macular corneal dystrophy types I and II in a single sibship 1998 ·British Journal of Ophthalmology ·Ningpu Liu,Jennifer Baldwin,Felicia Lennon,Jeffrey M. Stajich,Eugene J-M.A. Thonar,M. A. Pericak‐Vance,Gordon K. Klintworth,Jeffery M. Vance	14
12	Further exclusion of FSHD1B from the telomeric region of 10q 1997 ·Neurogenetics ·(unknown),M. A. Pericak‐Vance,Jeffrey M. Stajich,(unknown),Mark C. Jordan,Allen D. Roses,Jeffery M. Vance,(unknown)	2
13	Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation 1997 ·Neuromuscular Disorders ·Jeffrey M. Stajich,James M. Gilchrist,Felicia Lennon,Arnold Lee,Larry H. Yamaoka,B.L. Rosi,P. C. Gaskell,(unknown),(unknown),Allen D. Roses,Jeffery M. Vance,Margaret A. Pericak-Vance	6
14	Periodic Vestibulocerebellar Ataxia, an Autosomal Dominant Ataxia With Defective Smooth Pursuit, Is Genetically Distinct From Other Autosomal Dominant Ataxias 1996 ·Archives of Neurology ·K. F. Damji,R. Rand Allingham,Stephen C. Pollock,(unknown),(unknown),Jeffrey M. Stajich,Larry H. Yamaoka,Jeffery M. Vance,Margaret A Pericak‐Vance	58
15	Confirmation of linkage of oculopharyngel muscular dystrophy to chromosome 14q 11.2‐q13 1996 ·Annals of Neurology ·Jeffrey M. Stajich,Felicia Lennon,Arnold Lee,Larry H. Yamaoka,(unknown),P. C. Gaskell,Allen D. Roses,Jeffery M. Vance,Margaret A. Pericak‐Vance,James M. Gilchrist,(unknown)	9
16	Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B 1995 ·Journal of Medical Genetics ·John R. Gilbert,Marcy C. Speer,Jeffrey M. Stajich,Robert M. Clancy,(unknown),Hongyu Qiu,Larry H. Yamaoka,Arun Kumar,Jeffery M. Vance,Cameron Stewart,Marvin P. Rozear,Allen D. Roses	5
17	A Pvull polymorphism detected by pEW404 (D17S64) on chromosome 17 1991 ·Nucleic Acids Research ·(unknown),Jeffery M. Vance,Jeffrey M. Stajich,Allen D. Roses	1
18	Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2 1991 ·Genomics ·Jeffery M. Vance,David Barker,Larry H. Yamaoka,Jeffrey M. Stajich,(unknown),Wu-Yen Hung,Kenneth H. Fischbeck,Allen D. Roses,Margaret A. Pericak‐Vance	57
19	Confirmation of linkage in von Hippel-Lindau disease 1990 ·Genomics ·Jeffery M. Vance,(unknown),(unknown),Jeffrey M. Stajich,Larry H. Yamaoka,Allen D. Roses,Wu-Yen Hung,Margaret A. Pericak‐Vance	24
20	Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17 1989 ·Experimental Neurology ·Jeffery M. Vance,Geoffrey C. Nicholson,(unknown),Jeffrey M. Stajich,Celia Stewart,Mei Y. Speer,W.‐Y. Hung,(unknown),David Barker,Margaret A. Pericak‐Vance	156

About Jeffrey M. Stajich

Jeffrey M. Stajich is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 41 papers that have together received 1.7k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (10 papers), Genetic Neurodegenerative Diseases (10 papers) and Parkinson's Disease Mechanisms and Treatments (8 papers). The work is most often cited by research in Neurology (687 citations), Cellular and Molecular Neuroscience (712 citations) and Neurology (295 citations). Jeffrey M. Stajich has collaborated with scholars based in United States, Netherlands and Australia. Frequent co-authors include Jeffery M. Vance, B.L. Scott, William K. Scott, Eden R. Martin, Mark Stacy, Margaret A. Pericak‐Vance, Dana B. Hancock, Larry H. Yamaoka, Margaret A. Pericak‐Vance and Marcy C. Speer. Their work appears in journals such as Nucleic Acids Research, PLoS ONE 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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