Gerald F. Cox

11.2k citations

102 papers · 6.7k indexed · 3 hit papers · h-index 42

Cardiology and Cardiovascular Medicine top 0.5%
- Cardiomyopathy and Myosin Studies 15
Physiology top 1%
- Lysosomal Storage Disorders Research 42
Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders 9
Rheumatology top 1%
- Glycogen Storage Diseases and Myoclonus 11
Epidemiology top 2%
- Trypanosoma species research and implications 10
Organic Chemistry
- Carbohydrate Chemistry and Synthesis 14
Molecular Biology
- Mitochondrial Function and Pathology 8
Pathology and Forensic Medicine
- Biomedical Research and Pathophysiology 7

Co-authors: Steven E. Lipshultz Jeffrey A. Towbin Lynn A. Sleeper Steven D. Colan April M. Lowe E. John Orav Jane Messere Paul R. Lurie
Cited by: Cardiology and Cardiovascular Medicine Physiology Clinical Biochemistry
Journals: New England Journal of Medicine (1 paper)Proceedings of the National Academy of Sciences (2 papers)The Lancet (1 paper)
Partner nations: United States United Kingdom France

In The Last Decade

Gerald F. Cox

100 papers receiving 6.5k citations

Hit Papers

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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.

2006 JAMA
2003 New England Journal of Medicine
2002 The American Journal of Human Genetics

Peers

Countries citing papers authored by Gerald F. Cox

Since Specialization

Citations

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

Fields of papers citing papers by Gerald F. Cox

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Inter-rater reliability of video clips to assess for obstructive sleep apnea in children Sleep Medicine ·Sherri L. Katz,Henrietta Blinder,Naomi Dussah,Vid Bijelić,Nick Barrowman,Gerald F. Cox,A. Leitman,Refika Ersu	2025	1
2	Plasma glucosylsphingosine correlations with baseline disease burden and response to eliglustat in two clinical trials of previously untreated adults with Gaucher disease type 1 Molecular Genetics and Metabolism ·Michel Peterschmitt,Meredith C. Foster,Allena Ji,Marianne B. Zajdel,Gerald F. Cox	2023	4
3	Patient and caregiver perspectives on burden of disease manifestations in late-onset Tay-Sachs and Sandhoff diseases Orphanet Journal of Rare Diseases ·Nicole Lyn,Ruth Pulikottil-Jacob,Camille Rochmann,Robert Krupnick,Chad Gwaltney,N. Thomas Stephens,Julie Kissell,Gerald F. Cox,Tanya Fischer,Alaa Hamed	2020	6
4	The art and science of choosing efficacy endpoints for rare disease clinical trials American Journal of Medical Genetics Part A ·Gerald F. Cox	2018	22
5	Long-term hematological, visceral, and growth outcomes in children with Gaucher disease type 3 treated with imiglucerase in the International Collaborative Gaucher Group Gaucher Registry Molecular Genetics and Metabolism ·Amal El‐Beshlawy,Anna Tylki‐Szymańska,Ashok Vellodi,Nadia Belmatoug,Gregory A. Grabowski,Edwin H. Kolodny,Julie L. Batista,Gerald F. Cox,Pramod K. Mistry	2016	41
6	Successful within-patient dose escalation of olipudase alfa in acid sphingomyelinase deficiency Molecular Genetics and Metabolism ·Melissa Wasserstein,Simon Jones,Handrean Soran,George A. Díaz,Natalie Lippa,Beth L. Thurberg,Kerry Culm-Merdek,Elias Shamiyeh,Haig Inguilizian,Gerald F. Cox,Ana Cristina Puga	2015	70
7	Novel first-dose adverse drug reactions during a phase I trial of olipudase alfa (recombinant human acid sphingomyelinase) in adults with Niemann–Pick disease type B (acid sphingomyelinase deficiency) Genetics in Medicine ·Margaret M. McGovern,Melissa Wasserstein,Brian Kirmse,W. Lane Duvall,Thomas D. Schiano,Beth L. Thurberg,Susan Richards,Gerald F. Cox	2015	46
8	Recommendations for the development of rare disease drugs using the accelerated approval pathway and for qualifying biomarkers as primary endpoints Orphanet Journal of Rare Diseases ·Emil Kakkis,Mary O’Donovan,Gerald F. Cox,Mark P. Hayes,Federico Goodsaid,P.K. Tandon,Pat Furlong,Susan Boynton,Mladen Bozic,M Orfali,Mark Thornton	2015	36
9	Monoallelic expression of the human FOXP2 speech gene Proceedings of the National Academy of Sciences ·Abidemi Adegbola,Gerald F. Cox,Elizabeth M. Bradshaw,David A. Hafler,Alexander A. Gimelbrant,Andrew Chess	2014	30
10	Characteristics and outcomes of cardiomyopathy in children with Duchenne or Becker muscular dystrophy: A comparative study from the Pediatric Cardiomyopathy Registry American Heart Journal ·David Connuck,Lynn A. Sleeper,Steven D. Colan,Gerald F. Cox,Jeffrey A. Towbin,April M. Lowe,James D. Wilkinson,E. John Orav,Leigha Cuniberti,Bonnie Anne Salbert,Steven E. Lipshultz	2008	163
11	Abstract 2343: Outcomes in Children with Noonan Syndrome and Cardiomyopathy Circulation ·James D. Wilkinson,April M. Lowe,Bonnie Anne Salbert,Lynn A. Sleeper,Jeffrey A. Towbin,Steven D. Colan,Gerald F. Cox,David Connuck,Elizabeth Cadregari,Sarah K. Clunie,Jane Messere,Steven E. Lipshultz	2007	1
12	Encephalocraniocutaneous lipomatosis accompanied by the formation of bone cysts: Harboring clues to pathogenesis? American Journal of Medical Genetics Part A ·Ute Moog,Filip Roelens,Geert Mortier,H. J. Sijstermans,Mary Kelly,Gerald F. Cox,Caroline D. Robson,Virginia Kimonis	2007	32
13	A follow-up study of MPS I patients treated with laronidase enzyme replacement therapy for 6 years Molecular Genetics and Metabolism ·Monica Sifuentes,Robin Winkler Doroshow,Richard H. Hoft,Greg Mason,Irwin Walot,Michael J. Diament,Susan Okazaki,Kenneth R. Huff,Gerald F. Cox,Stuart J. Swiedler,Emil Kakkis	2006	183
14	Incidence, Causes, and Outcomes of Dilated Cardiomyopathy in Childrenbreakdown → JAMA ·Jeffrey A. Towbin,April M. Lowe,Steven D. Colan,Lynn A. Sleeper,E. John Orav,Sarah K. Clunie,Jane Messere,Gerald F. Cox,Paul R. Lurie,Daphne T. Hsu,Charles E. Canter,James D. Wilkinson,Steven E. Lipshultz	2006	647
15	Retinal Function in Carriers of Bardet-Biedl Syndrome Archives of Ophthalmology ·Gerald F. Cox	2003	17
16	Cardiac phenotypes in chromosome 4q− syndrome with and without a deletion of the dHAND gene Genetics in Medicine ·Taosheng Huang,Angela E. Lin,Gerald F. Cox,Wendy L. Golden,Gerald L. Feldman,Ute Moog,Connie Schrander‐Stumpel,Mitsuhiro Kamisago,Stefan Vermeulen	2002	29
17	Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defectsbreakdown → The American Journal of Human Genetics ·Gerald F. Cox,Joachim Bürger,Va Lip,Ulrike Mau,Karl Sperling,Bai‐Lin Wu,Bernhard Horsthemke	2002	519
18	Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome Nature Genetics ·Kirk Mykytyn,Darryl Nishimura,Charles Searby,Mythreyi Shastri,Hsan-Jan Yen,John S. Beck,Terry A. Braun,Luan M. Streb,Alberto S. Cornier,Gerald F. Cox,Anne B. Fulton,Rivka Carmi,Güven Lüleci,Settara C. Chandrasekharappa,Francis S. Collins,Samuel G. Jacobson,John R. Heckenlively,Richard G. Weleber,Edwin M. Stone,Val C. Sheffield	2002	258
19	Contiguous Deletion of the X-Linked Adrenoleukodystrophy Gene (ABCD1) and DXS1357E: A Novel Neonatal Phenotype Similar to Peroxisomal Biogenesis Disorders The American Journal of Human Genetics ·Deyanira Corzo,William T. Gibson,Kisha Johnson,Grant A. Mitchell,Guy LePage,Gerald F. Cox,Robin Casey,Carolyn Zeiss,Heidi Tyson,Garry R. Cutting,Gerald V. Raymond,Kirby D. Smith,Paul A. Watkins,Ann B. Moser,Hugo W. Moser,Steven J. Steinberg	2002	50
20	Etiology and family history of pediatric cardiomyopathy: the early pediatric cardiomyopathy registry (PCMR) experience Journal of the American College of Cardiology ·S.E. Lipshultz,Jeffrey A. Towbin,Michelle A. Grenier,Voula Osganian,S D Colan,Lynn A. Sleeper,Robert E. Shaddy,Gerald F. Cox,Paul R. Lurie	1998	1

About Gerald F. Cox

Gerald F. Cox is a scholar working on Physiology, Clinical Biochemistry and Rheumatology, having authored 102 papers that have together received 6.7k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (42 papers), Cardiomyopathy and Myosin Studies (15 papers), Carbohydrate Chemistry and Synthesis (14 papers), Glycogen Storage Diseases and Myoclonus (11 papers), Trypanosoma species research and implications (10 papers), Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (8 papers) and Biomedical Research and Pathophysiology (7 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (2.2k citations), Physiology (2.0k citations) and Clinical Biochemistry (338 citations). Gerald F. Cox has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Steven E. Lipshultz, Jeffrey A. Towbin, Lynn A. Sleeper, Steven D. Colan, April M. Lowe, E. John Orav, Jane Messere, Paul R. Lurie, James D. Wilkinson and Louis M. Kunkel. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

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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