Jane S. Green

4.3k citations

31 papers · 1.8k indexed · h-index 19

Co-authors: Patrick S. Parfrey William S. Davidson Michael O. Woods Nicholas Katsanis Philip L. Beales Stephen J. Ansley Terry‐Lynn Young Susan Moore
Topics: Genetic Syndromes and Imprinting (12 papers)Genetic and Kidney Cyst Diseases (12 papers)Genetic factors in colorectal cancer (8 papers)
Cited by: Genetics Molecular Biology Pathology and Forensic Medicine
Journals: New England Journal of Medicine Nature Genetics Scientific Reports
Partner nations: Canada United States United Kingdom

In The Last Decade

Jane S. Green

31 papers receiving 1.7k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Retinal Dystrophy Associated With RLBP1 Retinitis Pigmentosa: A Five-Year Prospective Natural History Study 2023 ·Investigative Ophthalmology & Visual Science ·Marie Burstedt,(unknown),Jane S. Green,Karen Holopigian,(unknown),Erin Greco,(unknown),Michael Wald,Cynthia L. Grosskreutz,Xiao Ni,Guillaume Normand,(unknown),(unknown),Michael Rosol,Yunsheng He,(unknown)	4
2	A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features 2020 ·Scientific Reports ·(unknown),Jane S. Green,Somayyeh Fahiminiya,Jacek Majewski,Bridget A. Fernandez,Matthew A. Deardorff,(unknown),(unknown),Dirk Hubmacher,Suneel Apte,Kym M. Boycott,Dennis E. Bulman,David A. Dyment,(unknown),Michael Brudno,Michael O. Woods	14
3	Impact of colonoscopic screening in Familial Colorectal Cancer Type X 2018 ·Molecular Genetics & Genomic Medicine ·(unknown),Jane S. Green,Michael O. Woods,(unknown),Patrick S. Parfrey	7
4	Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland 2017 ·Familial Cancer ·(unknown),Jane S. Green,Michael O. Woods	2
5	Novel 25 kb Deletion of MERTK Causes Retinitis Pigmentosa With Severe Progression 2017 ·Investigative Ophthalmology & Visual Science ·(unknown),Jane S. Green,(unknown),Jeremy Schwartzentruber,Jacek Majewski,Chandree L. Beaulieu,Wen Qin,Christian R. Marshall,Tara Paton,Nicole M. Roslin,Andrew D. Paterson,Somayyeh Fahiminiya,(unknown),Kym M. Boycott,Michael O. Woods	13
6	Genetic structure of the Newfoundland and Labrador population: founder effects modulate variability 2015 ·European Journal of Human Genetics ·Guangju Zhai,Jiayi Zhou,Michael O. Woods,Jane S. Green,Patrick S. Parfrey,Proton Rahman,Roger C. Green	19
7	Inherited deleterious variants inGALNT12are associated with CRC susceptibility 2012 ·Human Mutation ·(unknown),Roger C. Green,Jane S. Green,(unknown),Patrick S. Parfrey,H. Banfield Younghusband,Michael O. Woods	40
8	Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype 2012 ·BMC Medical Genetics ·Bridget A. Fernandez,Jane S. Green,Ford Bursey,Brendan J. Barrett,Andrée MacMillan,(unknown),(unknown),Proton Rahman,(unknown),Sérgio L. Pereira,Stephen W. Scherer,Kym M. Boycott,Michael O. Woods	13
9	Lynch syndrome: barriers to and facilitators of screening and disease management 2011 ·Hereditary Cancer in Clinical Practice ·Katherine E. Watkins,Christine Way,(unknown),Robert J. Meadus,Mary Jane Esplen,Jane S. Green,(unknown),Holly Etchegary,Patrick S. Parfrey	30
10	Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 2008 ·European Journal of Human Genetics ·Lance P. Doucette,Nancy D. Merner,(unknown),Elizabeth Ives,(unknown),(unknown),Tom Walsh,(unknown),(unknown),Bridget A. Fernandez,Jane S. Green,Edward R. Wilcox,(unknown),(unknown),Ming Lee,Mary‐Claire King,Terry‐Lynn Young	30
11	The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome 2006 ·Familial Cancer ·Susan Stuckless,Patrick S. Parfrey,Michael O. Woods,(unknown),(unknown),Jane S. Green,Roger C. Green	21
12	High Frequency of Hereditary Colorectal Cancer in Newfoundland Likely Involves Novel Susceptibility Genes 2005 ·Clinical Cancer Research ·Michael O. Woods,(unknown),(unknown),Susan Stuckless,Jane S. Green,Aaron Pollett,J. Desmond Robb,Roger C. Green,Marina E. Croitoru,(unknown),(unknown),(unknown),Esther M. John,Steven Gallinger,H. Banfield Younghusband,Bharati Bapat,Patrick S. Parfrey	45
13	Linkage disequilibrium mapping in the Newfoundland population: a re-evaluation of the refinement of the Bardet?Biedl syndrome 1 critical interval 2004 ·Human Genetics ·Yanli Fan,Jane S. Green,Alison Ross,Philip L. Beales,Patrick S. Parfrey,William S. Davidson	3
14	Newfoundland Rod-Cone Dystrophy, an Early-Onset Retinal Dystrophy, Is Caused by Splice-Junction Mutations in RLBP1 2002 ·The American Journal of Human Genetics ·Erica R. Eichers,Jane S. Green,David W. Stockton,(unknown),(unknown),J. Arch McNamara,(unknown),James R. Lupski,Nicholas Katsanis	70
15	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 2001 ·The American Journal of Human Genetics ·Philip L. Beales,Nicholas Katsanis,Richard A. Lewis,Stephen J. Ansley,Nursel Elçioğlu,Jamal Raza,Michael O. Woods,Jane S. Green,Patrick S. Parfrey,William S. Davidson,James R. Lupski	57
16	Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome 2000 ·Nature Genetics ·Nicholas Katsanis,Philip L. Beales,Michael O. Woods,Richard A. Lewis,Jane S. Green,Patrick S. Parfrey,Stephen J. Ansley,William S. Davidson,James R. Lupski	224
17	Mutations in MKKS cause Bardet-Biedl syndrome 2000 ·Nature Genetics ·Anne Slavotinek,Edwin M. Stone,Kirk Mykytyn,John R. Heckenlively,Jane S. Green,Elise Héon,Maria A. Musarella,Patrick S. Parfrey,Val C. Sheffield,Leslie G. Biesecker	195
18	A Fifth Locus for Bardet-Biedl Syndrome Maps to Chromosome 2q31 1999 ·The American Journal of Human Genetics ·Terry‐Lynn Young,Lynette S. Penney,Michael O. Woods,Patrick S. Parfrey,Jane S. Green,Donna Hefferton,William S. Davidson	90
19	Common ancestral mutations in theMEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland 1998 ·Human Mutation ·Shodimu-Emmanuel Olufemi,Jane S. Green,Pachiappan Manickam,Siradanahalli C. Guru,Sunita Agarwal,Mary Beth Kester,Qihan Dong,A. Lee Burns,Allen M. Spiegel,Stephen J. Marx,Francis S. Collins,Settara C. Chandrasekharappa	83
20	The Spectrum of Renal Disease in Laurence–Moon–Biedl Syndrome 1988 ·New England Journal of Medicine ·John D. Harnett,Jane S. Green,B. Cramer,(unknown),L. Chafe,P J McManamon,Nadir R. Farid,William Pryse‐Phillips,Patrick S. Parfrey	117

About Jane S. Green

Jane S. Green is a scholar working on Genetics, Pathology and Forensic Medicine and Ophthalmology, having authored 31 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (12 papers), Genetic and Kidney Cyst Diseases (12 papers) and Genetic factors in colorectal cancer (8 papers). The work is most often cited by research in Genetics (1.2k citations), Molecular Biology (1.1k citations) and Pathology and Forensic Medicine (256 citations). Jane S. Green has collaborated with scholars based in Canada, United States and United Kingdom. Frequent 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. Their work appears in journals such as New England Journal of Medicine, Nature Genetics and Scientific Reports.

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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