Felicia Lennon

1.5k citations

21 papers · 991 indexed · h-index 15

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

Co-authors: Jeffery M. Vance Margaret A. Pericak‐Vance Allen D. Roses Kamel Ben Othmane Margaret A Pericak‐Vance E.A. Helmbold Marcy C. Speer Monica A. De La Paz
Topics: Hereditary Neurological Disorders (8 papers)Neurological diseases and metabolism (5 papers)Retinal Diseases and Treatments (4 papers)
Cited by: Neurology Ophthalmology Cellular and Molecular Neuroscience
Journals: Journal of Clinical Investigation Neurology Annals of Neurology
Partner nations: United States Cyprus United Kingdom

In The Last Decade

Felicia Lennon

21 papers receiving 964 citations

Peers

Countries citing papers authored by Felicia Lennon

Since Specialization

Citations

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

Fields of papers citing papers by Felicia Lennon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Felicia Lennon. 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 Felicia Lennon. The network helps show where Felicia Lennon may publish in the future.

Co-authorship network of co-authors of Felicia Lennon

This figure shows the co-authorship network connecting the top 25 collaborators of Felicia Lennon. A scholar is included among the top collaborators of Felicia Lennon 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 Felicia Lennon. Felicia Lennon 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	North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysis. 1999 ·PubMed ·Kent W. Small,Nitin Udar,(unknown),Robert R. Klein,Charles García,Guillermo Gallardo Madueño,Bernard Puech,Virginie Puech,David A. Saperstein,Jennifer I. Lim,József Haller,Christina J. Flaxel,Rosemary E. Kelsell,David M. Hunt,Kevin Gregory-Evans,Felicia Lennon,M. A. Pericak‐Vance	36
2	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
3	Evidence for Genetic Heterogeneity Supports Clinical Differences in Congenital Myasthenic Syndromes 1998 ·Human Heredity ·Marisa M. Menold,Menachem Sadeh,Felicia Lennon,Ilan Blatt,Yochanan Goldhammer,Larry H. Yamaoka,Jeffery M. Vance,Margaret A. Pericak‐Vance	2
4	Exclusion of TIMP3 as a Candidate Locus in Age-related Macular Degeneration 1998 ·Retina ·Monica A. De La Paz,Margaret A. Pericak‐Vance,Felicia Lennon,J. L. Haines,J.M. Seddon	13
5	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
6	Familial spastic paraparesis: Evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2 1997 ·American Journal of Medical Genetics ·Wendy H. Raskind,Margaret A. Pericak‐Vance,Felicia Lennon,John Wolff,Hillary Lipe,Thomas D. Bird	21
7	Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13. 1997 ·Journal of Clinical Investigation ·Michael J. Econs,Paul T. McEnery,Felicia Lennon,Marcy C. Speer	69
8	Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity 1997 ·Neurogenetics ·Jeffery M. Vance,Marcy C. Speer,Felicia Lennon,Sandra G. West,Marisa M. Menold,Jeffrey M. Stajich,Chantelle M. Wolpert,Brandon D. Slotterbeck,Mikito Saito,Richard W. Tim,Marvin P. Rozear,Lefkos Middleton,Shoji Tsuji	18
9	Exclusion of TIMP3 as a candidate locus in age-related macular degeneration. 1997 ·PubMed ·Monica A. De La Paz,Margaret A. Pericak‐Vance,Felicia Lennon,J. L. Haines,Johanna M. Seddon	77
10	Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia 1997 ·Neurogenetics ·William K. Scott,P. C. Gaskell,Felicia Lennon,Chantelle M. Wolpert,Marisa M. Menold,Arthur S. Aylsworth,Carolyn L. Warner,Carolyn Farrell,(unknown),Susan G. Albright,(unknown),Helen Kingston,W. J. K. Cumming,Jeffery M. Vance	17
11	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
12	Linkage of a gene for macular corneal dystrophy to chromosome 16. 1996 ·PubMed ·Jeffery M. Vance,Friðbert Jónasson,Felicia Lennon,(unknown),Karim F. Damji,Jennifer E. Stauffer,Margaret A Pericak‐Vance,(unknown)	69
13	A gene for familial venous malformations maps to chromosome 9p in a second large kindred. 1995 ·Journal of Medical Genetics ·Carol J. Gallione,Krystyna A. Pasyk,Laurence M. Boon,Felicia Lennon,David W. Johnson,E.A. Helmbold,Dorene S. Markel,Miikka Vikkula,John B. Mulliken,Matthew L. Warman	105
14	Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype. 1994 ·Journal of Medical Genetics ·Kimberly A. McAllister,Felicia Lennon,(unknown),Wendy McKinnon,E.A. Helmbold,Dorene S. Markel,Charles E. Jackson,Alan E. Guttmacher,M. A. Pericak‐Vance,Douglas A. Marchuk	79
15	Genetic heterogeneity in hereditary hemorrhagic telangiectasia: Possible correlation with clinical phenotype 1994 ·The American Journal of Human Genetics ·(unknown),Felicia Lennon,E.A. Helmbold	9
16	Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers 1994 ·Human Molecular Genetics ·Afif Hentati,Margaret A. Pericak‐Vance,Felicia Lennon,(unknown),Fayçal Hentati,T.R. Juneja,Misha Angrist,W.‐Y. Hung,Rose-Mary Boustany,Saeed Bohlega,Zafar Iqbal,(unknown),Mongi Ben Hamida,Teepu Siddique	71
17	Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity 1993 ·Genomics ·Kamel Ben Othmane,Lefkos Middleton,(unknown),(unknown),Felicia Lennon,Marvin P. Rozear,(unknown),P. C. Gaskell,Allen D. Roses,Margaret A. Pericak‐Vance,Jeffery M. Vance	120
18	Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q 1993 ·Human Molecular Genetics ·Kamel Ben Othmane,(unknown),Felicia Lennon,Christiane Ben Hamida,(unknown),A.D. Roses,Margaret A Pericak‐Vance,M. Ben Hamida,Jeffery M. Vance	136
19	North Carolina macular dystrophy is assigned to chromosome 6 1992 ·Genomics ·(unknown),James L. Weber,Allen D. Roses,Felicia Lennon,Jeffery M. Vance,Margaret A. Pericak‐Vance	100
20	Linkage studies in Charcot‐Marie‐Tooth disease type 2 1992 ·Neurology ·(unknown),M. A. Pericak‐Vance,Jeffrey M. Stajich,P. C. Gaskell,(unknown),Felicia Lennon,Larry H. Yamaoka,Allen D. Roses,Jeffery M. Vance	18

About Felicia Lennon

Felicia Lennon is a scholar working on Neurology, Genetics and Ophthalmology, having authored 21 papers that have together received 991 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (8 papers), Neurological diseases and metabolism (5 papers) and Retinal Diseases and Treatments (4 papers). The work is most often cited by research in Neurology (210 citations), Ophthalmology (209 citations) and Cellular and Molecular Neuroscience (386 citations). Felicia Lennon has collaborated with scholars based in United States, Cyprus and United Kingdom. Frequent co-authors include Jeffery M. Vance, Margaret A. Pericak‐Vance, Allen D. Roses, Kamel Ben Othmane, Margaret A Pericak‐Vance, Margaret A. Pericak‐Vance, E.A. Helmbold, Marcy C. Speer, Monica A. De La Paz and Dorene S. Markel. Their work appears in journals such as Journal of Clinical Investigation, Neurology and Annals of 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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