Jane S. Green

4.3k total citations
31 papers, 1.8k citations indexed

About

Jane S. Green is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Jane S. Green has authored 31 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 15 papers in Molecular Biology and 10 papers in Pathology and Forensic Medicine. Recurrent topics in Jane S. Green's work include Genetic Syndromes and Imprinting (12 papers), Genetic and Kidney Cyst Diseases (12 papers) and Genetic factors in colorectal cancer (8 papers). Jane S. Green is often cited by papers focused on Genetic Syndromes and Imprinting (12 papers), Genetic and Kidney Cyst Diseases (12 papers) and Genetic factors in colorectal cancer (8 papers). Jane S. Green collaborates with scholars based in Canada, United States and United Kingdom. Jane S. Green's co-authors include Patrick S. Parfrey, William S. Davidson, Michael O. Woods, Nicholas Katsanis, Philip L. Beales, Stephen J. Ansley, Terry‐Lynn Young, Susan Moore, Yanli Fan and Donna Hefferton and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and Scientific Reports.

In The Last Decade

Jane S. Green

31 papers receiving 1.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jane S. Green Canada 19 1.2k 1.1k 256 176 147 31 1.8k
Julie Désir Belgium 19 529 0.4× 676 0.6× 73 0.3× 268 1.5× 85 0.6× 46 1.4k
Steffen Uebe Germany 22 507 0.4× 819 0.7× 98 0.4× 134 0.8× 99 0.7× 58 1.3k
Marie McDonald United States 19 1.1k 0.9× 749 0.7× 121 0.5× 239 1.4× 50 0.3× 45 1.7k
Gayle B. Collin United States 25 1.5k 1.2× 1.1k 1.0× 74 0.3× 144 0.8× 30 0.2× 47 2.1k
Sibel Kantarci United States 15 1.0k 0.8× 821 0.8× 126 0.5× 62 0.4× 32 0.2× 23 1.8k
Hester Y. Kroes Netherlands 19 1.0k 0.8× 973 0.9× 76 0.3× 121 0.7× 45 0.3× 38 1.5k
Süleyman Gülsüner United States 21 736 0.6× 795 0.7× 186 0.7× 92 0.5× 296 2.0× 43 1.7k
Mirella Bruttini Italy 22 777 0.6× 1.0k 0.9× 39 0.2× 234 1.3× 109 0.7× 40 1.6k
A Seller United Kingdom 15 797 0.7× 940 0.9× 37 0.1× 147 0.8× 58 0.4× 24 1.7k
Kay Huebner United States 11 599 0.5× 1.1k 1.0× 149 0.6× 97 0.6× 213 1.4× 14 1.6k

Countries citing papers authored by Jane S. Green

Since Specialization
Citations

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

Fields of papers citing papers by Jane S. Green

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jane S. Green. 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 Jane S. Green. The network helps show where Jane S. Green may publish in the future.

Co-authorship network of co-authors of Jane S. Green

This figure shows the co-authorship network connecting the top 25 collaborators of Jane S. Green. A scholar is included among the top collaborators of Jane S. Green 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 Jane S. Green. Jane S. Green is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Burstedt, Marie, Jane S. Green, Karen Holopigian, et al.. (2023). Retinal Dystrophy Associated With RLBP1 Retinitis Pigmentosa: A Five-Year Prospective Natural History Study. Investigative Ophthalmology & Visual Science. 64(13). 42–42. 4 indexed citations
2.
Green, Jane S., Somayyeh Fahiminiya, Jacek Majewski, et al.. (2020). A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features. Scientific Reports. 10(1). 10827–10827. 14 indexed citations
3.
Green, Jane S., et al.. (2018). Impact of colonoscopic screening in Familial Colorectal Cancer Type X. Molecular Genetics & Genomic Medicine. 6(6). 1021–1030. 7 indexed citations
4.
Green, Jane S., et al.. (2017). Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland. Familial Cancer. 17(2). 205–208. 2 indexed citations
5.
Green, Jane S., Jeremy Schwartzentruber, Jacek Majewski, et al.. (2017). Novel 25 kb Deletion of MERTK Causes Retinitis Pigmentosa With Severe Progression. Investigative Ophthalmology & Visual Science. 58(3). 1736–1736. 13 indexed citations
6.
Zhai, Guangju, Jiayi Zhou, Michael O. Woods, et al.. (2015). Genetic structure of the Newfoundland and Labrador population: founder effects modulate variability. European Journal of Human Genetics. 24(7). 1063–1070. 19 indexed citations
7.
Green, Roger C., et al.. (2012). Inherited deleterious variants inGALNT12are associated with CRC susceptibility. Human Mutation. 33(7). 1056–1058. 40 indexed citations
8.
Fernandez, Bridget A., Jane S. Green, Ford Bursey, et al.. (2012). Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype. BMC Medical Genetics. 13(1). 111–111. 13 indexed citations
9.
Watkins, Katherine E., Christine Way, Robert J. Meadus, et al.. (2011). Lynch syndrome: barriers to and facilitators of screening and disease management. Hereditary Cancer in Clinical Practice. 9(1). 8–8. 30 indexed citations
10.
Doucette, Lance P., Nancy D. Merner, Elizabeth Ives, et al.. (2008). Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15. European Journal of Human Genetics. 17(5). 554–564. 30 indexed citations
11.
Stuckless, Susan, et al.. (2006). The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome. Familial Cancer. 6(1). 1–12. 21 indexed citations
12.
Woods, Michael O., Susan Stuckless, Jane S. Green, et al.. (2005). High Frequency of Hereditary Colorectal Cancer in Newfoundland Likely Involves Novel Susceptibility Genes. Clinical Cancer Research. 11(19). 6853–6861. 45 indexed citations
13.
Fan, Yanli, Jane S. Green, Alison Ross, et al.. (2004). Linkage disequilibrium mapping in the Newfoundland population: a re-evaluation of the refinement of the Bardet?Biedl syndrome 1 critical interval. Human Genetics. 116(1-2). 62–71. 3 indexed citations
14.
Eichers, Erica R., Jane S. Green, David W. Stockton, et al.. (2002). Newfoundland Rod-Cone Dystrophy, an Early-Onset Retinal Dystrophy, Is Caused by Splice-Junction Mutations in RLBP1. The American Journal of Human Genetics. 70(4). 955–964. 70 indexed citations
15.
Beales, Philip L., Nicholas Katsanis, Richard A. Lewis, et al.. (2001). Genetic and Mutational Analyses of a Large Multiethnic Bardet-Biedl Cohort Reveal a Minor Involvement of BBS6 and Delineate the Critical Intervals of Other Loci. The American Journal of Human Genetics. 68(3). 606–616. 57 indexed citations
16.
Katsanis, Nicholas, Philip L. Beales, Michael O. Woods, et al.. (2000). Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome. Nature Genetics. 26(1). 67–70. 224 indexed citations
17.
Slavotinek, Anne, Edwin M. Stone, Kirk Mykytyn, et al.. (2000). Mutations in MKKS cause Bardet-Biedl syndrome. Nature Genetics. 26(1). 15–16. 195 indexed citations
18.
Young, Terry‐Lynn, Lynette S. Penney, Michael O. Woods, et al.. (1999). A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31. The American Journal of Human Genetics. 64(3). 900–904. 90 indexed citations
19.
Olufemi, Shodimu-Emmanuel, Jane S. Green, Pachiappan Manickam, et al.. (1998). Common ancestral mutations in theMEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland. Human Mutation. 11(4). 264–269. 83 indexed citations
20.
Harnett, John D., Jane S. Green, B. Cramer, et al.. (1988). The Spectrum of Renal Disease in Laurence–Moon–Biedl Syndrome. New England Journal of Medicine. 319(10). 615–618. 117 indexed citations

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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