Sherryl A. Taylor

1.2k citations

35 papers · 768 indexed · h-index 16

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

Co-authors: David Lillicrap Marcy E. MacDonald Richard H. Myers Jayalakshmi Srinidhi James F. Gusella Carol Sze Ki Lin Glenn Barnes Mabel P. Duyao
Topics: Hemophilia Treatment and Research (9 papers)Cancer-related gene regulation (9 papers)Blood Coagulation and Thrombosis Mechanisms (8 papers)
Cited by: Cellular and Molecular Neuroscience Neurology Hematology
Journals: Nucleic Acids Research Nature Genetics Neurology
Partner nations: Canada United States United Kingdom

In The Last Decade

Sherryl A. Taylor

34 papers receiving 731 citations

Peers

Replace John Wolff with:

John Wolff United States

Timothy W. Vogel United States

Laurence E. Walsh United States

Dong-Hui Chen United States

Thalia Antoniadi Greece

Friedmar R. Kreuz Germany

Cecily E. Hamill United States

Christel Thauvin‐Robinet France

V. Volpini Spain

M Schmidt United States

Sherryl A. Taylor relative to John Wolff United States John Wolff's profile →

Citations per field

00.5×1.5×

John Wolff · 1×

×0.9 455/481

MB

×0.8 318/411

CMN

×1.2 181/154

NEURO

×1.0 137/137

GENET

×1.3 131/101

HEMAT

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Countries citing papers authored by Sherryl A. Taylor

Since Specialization

Citations

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

Fields of papers citing papers by Sherryl A. Taylor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sherryl A. Taylor. 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 Sherryl A. Taylor. The network helps show where Sherryl A. Taylor may publish in the future.

Co-authorship network of co-authors of Sherryl A. Taylor

This figure shows the co-authorship network connecting the top 25 collaborators of Sherryl A. Taylor. A scholar is included among the top collaborators of Sherryl A. Taylor 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 Sherryl A. Taylor. Sherryl A. Taylor 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	The Influence of Smoking and Occupational Risk Factors on DNA Methylation in the AHRR and F2RL3 Genes 2023 ·Cancer Epidemiology Biomarkers & Prevention ·(unknown),(unknown),(unknown),(unknown),Sherryl A. Taylor,(unknown),Anita Koushik,Vikki Ho	1
2	Gene-specific DNA methylation of DNMT3B and MTHFR and colorectal adenoma risk 2015 ·Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Vikki Ho,(unknown),Sherryl A. Taylor,Stephen Vanner,Will D. King	8
3	A cross-sectional study of global DNA methylation and risk of colorectal adenoma 2014 ·BMC Cancer ·Will D. King,(unknown),Sherryl A. Taylor,M. Yat Tse,Stephen C. Pang,(unknown),Stephen Vanner	25
4	Biomarkers measured in buccal and blood leukocyte DNA as proxies for colon tissue global methylation. 2014 ·PubMed ·(unknown),Sherryl A. Taylor,(unknown),Stephen C. Pang,(unknown),(unknown),(unknown)	6
5	Noninvasive investigation of asymmetrically conjoined tripus twins with features of rachipagus, parapagus dicephalus, and cephalopagus 2011 ·Clinical Anatomy ·(unknown),(unknown),Omar Islam,Jennifer MacKenzie,Sherryl A. Taylor,Stephen C. Pang,C. W. Reifel	1
6	The aero2 ( aeromaculata2) mutation in pea increases leaf flecking and complexity but, unlike aero1, does not promote flowering 2004 ·eCite Digital Repository (University of Tasmania) ·(unknown),Sherryl A. Taylor	0
7	A model for GFRα4 function and a potential modifying role in multiple endocrine neoplasia 2 2004 ·Oncogene ·(unknown),Scott D. Andrew,Karen J. Harrison,Sherryl A. Taylor,Bradley Thomas,Thomas J. McDonald,Peter Ainsworth,Lois M. Mulligan	9
8	Paternal transmission of fragile X syndrome 2004 ·American Journal of Medical Genetics Part A ·Susan Zeesman,Lonnie Zwaigenbaum,Donald T. Whelan,Randi J. Hagerman,Flora Tassone,Sherryl A. Taylor	35
9	Genetic Basis of Familial Meniere's Disease 2002 ·The Journal of Otolaryngology ·Kevin Fung,Ying Xie,Stephen F. Hall,David Lillicrap,Sherryl A. Taylor	26
10	PREVALENCE OF FACTOR V LEIDEN AND ACTIVATED PROTEIN C RESISTANCE IN CENTRAL RETINAL VEIN OCCLUSION 2001 ·Retina ·(unknown),Sherif El-Defrawy,William Hodge,Brian C. Leonard,Peter J. Kertes,Sherryl A. Taylor,David Lillicrap	21
11	Mutation of RET codon 768 is associated with the FMTC phenotype 1997 ·Clinical Genetics ·(unknown),Jane S. Green,Carol Joyce,Charis Eng,Sherryl A. Taylor,(unknown)	31
12	Adult-onset neurodegenerative disorder due to proteolipid protein gene mutation in the mother of a man with Pelizaeus-Merzbacher disease 1996 ·Neurology ·Martha Nance,(unknown),Victoria M. Pratt,Sherryl A. Taylor,M. E. Hodes,S. R. Dlouhy	27
13	De novo expansion of a (CAG)n repeat in sporadic Huntington's disease 1993 ·Nature Genetics ·Richard H. Myers,Marcy E. MacDonald,Walter J. Koroshetz,Mabel P. Duyao,C M Ambrose,Sherryl A. Taylor,Glenn Barnes,Jayalakshmi Srinidhi,Carol Sze Ki Lin,William L. Whaley,Alice Lazzarini,Michael Schwarz,G. Wolff,E. D. Bird,J.-P. G. Vonsattel,James F. Gusella	184
14	A gene from chromosome 4p 16.3 with similarity to a superfamily of transporter proteins 1993 ·Human Molecular Genetics ·Mabel P. Duyao,Sherryl A. Taylor,Alan Buckler,Christine Ambrose,Carol Sze Ki Lin,(unknown),Deanna M. Church,Glenn Barnes,John J. Wasmuth,David E. Housman,Marcy E. MacDonald,James F. Gusella	18
15	Differential termination of primer extension: a novel, quantifiable method for detection of point mutations 1992 ·Human Genetics ·David J. Picketts,Charles J. Cameron,Sherryl A. Taylor,(unknown),(unknown)	12
16	A mutation adjacent to the beta cleavage site of factor IX (valine 182 to leucine) results in mild haemophilia B_m 1990 ·British Journal of Haematology ·Sherryl A. Taylor,(unknown),I. R. Peake,A L Bloom,D Lillicrap	17
17	A past mutation at Isoleucine³⁹⁷ is now a common cause of moderate/mild haemophilia B 1990 ·British Journal of Haematology ·C. D. K. Bottema,(unknown),Rhett P. Ketterling,E. J. Walter Bowie,Sherryl A. Taylor,David Lillicrap,Amy Shapiro,Gerald Gilchrist,(unknown)	31
18	Factor IX Cardiff: a variant factor IX protein that shows abnormal activation is caused by an arginine to cysteine substitution at position 145 1989 ·British Journal of Haematology ·(unknown),I R Peake,Sherryl A. Taylor,David Lillicrap,J. C. Giddings,A L Bloom	13
19	A BstXI polymorphism detected by the factor VIII genomic probe p.482.6 (F8C) 1989 ·Nucleic Acids Research ·Sherryl A. Taylor,Peter J. Bridge,D Lillicrap	2
20	A complete deletion of the factor IX gene and new TaqI variant in a hemophilia B kindred 1988 ·Human Genetics ·Sherryl A. Taylor,David Lillicrap,V. Blanchette,Alan R. Giles,Jeanette J. A. Holden,Bradley N. White	5

About Sherryl A. Taylor

Sherryl A. Taylor is a scholar working on Hematology, Genetics and Molecular Biology, having authored 35 papers that have together received 768 indexed citations. Recurring topics across this work include Hemophilia Treatment and Research (9 papers), Cancer-related gene regulation (9 papers) and Blood Coagulation and Thrombosis Mechanisms (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (318 citations), Neurology (181 citations) and Hematology (131 citations). Sherryl A. Taylor has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include David Lillicrap, Marcy E. MacDonald, Richard H. Myers, Jayalakshmi Srinidhi, James F. Gusella, Carol Sze Ki Lin, Glenn Barnes, Mabel P. Duyao, Alice Lazzarini and Michael Schwarz. Their work appears in journals such as Nucleic Acids Research, Nature Genetics 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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