Annette K. Taylor

7.0k citations

77 papers · 5.5k indexed · 1 hit paper · h-index 40

Genetics top 0.2%
Cognitive Neuroscience top 0.5%
Molecular Biology top 2%
Clinical Psychology top 5%
Cellular and Molecular Neuroscience top 5%

Co-authors: Randi J. Hagerman Flora Tassone Paul J. Hagerman Louise W. Gane Danuta Z. Loesch Tony E. Godfrey Richard Huggins Minh Bui
Topics: Genetics and Neurodevelopmental Disorders (54 papers)Autism Spectrum Disorder Research (38 papers)Genomic variations and chromosomal abnormalities (17 papers)
Cited by: Cognitive Neuroscience Genetics Molecular Biology
Journals: Science Proceedings of the National Academy of Sciences JAMA
Partner nations: United States Australia Sweden

In The Last Decade

Annette K. Taylor

76 papers receiving 5.3k citations

Hit Papers

align trajectories

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.

Elevated Levels of FMR1 mRNA in Carrier Males: A New Mechanism of Involvement in the Fragile-X Syndrome

2000 655 citations Flora Tassone, Randi J. Hagerman et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by Annette K. Taylor

Since Specialization

Citations

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

Fields of papers citing papers by Annette K. Taylor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annette K. Taylor

This figure shows the co-authorship network connecting the top 25 collaborators of Annette K. Taylor. A scholar is included among the top collaborators of Annette K. 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 Annette K. Taylor. Annette K. 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	Accuracy and reproducibility of latent print decisions on comparisons from searches of an automated fingerprint identification system 2025 ·Forensic Science International ·R. Austin Hicklin,(unknown),Annette K. Taylor,JoAnn Buscaglia	1
2	Moving Pharmacogenetics Into Practice: It’s All About the Evidence! 2021 ·Clinical Pharmacology & Therapeutics ·Jasmine A. Luzum,Natasha Petry,Annette K. Taylor,Sara L. Van Driest,Henry M. Dunnenberger,Larisa H. Cavallari	40
3	Common-variant associations with fragile X syndrome 2018 ·Molecular Psychiatry ·James J. Crowley,Jin Szatkiewicz,Anna K. Kähler,Paola Giusti‐Rodríguez,(unknown),Jessica K. Booker,(unknown),(unknown),Molly Losh,Craig A. Stockmeier,Annette K. Taylor,Joseph Piven,Patrick F. Sullivan	6
4	Lack of Serologic Evidence to Link IgA Nephropathy with Celiac Disease or Immune Reactivity to Gluten 2014 ·PLoS ONE ·(unknown),Pietro A. Canetta,Annette K. Taylor,Carolina Argüelles-Grande,Holly J. Snyder,Peter H. Green,Krzysztof Kiryluk,Armin Alaedini	25
5	Fragile X‐associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene 2011 ·Clinical Genetics ·Danuta Z. Loesch,(unknown),Glynda Kinsella,F. Tassone,Annette K. Taylor,David J. Amor,(unknown),Andrew Evans	56
6	Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: A new perspective 2002 ·American Journal of Medical Genetics Part A ·Danuta Z. Loesch,Richard Huggins,Minh Bui,Annette K. Taylor,Randi J. Hagerman	36
7	Functional Neuroanatomy of Visuospatial Working Memory in Fragile X Syndrome: Relation to Behavioral and Molecular Measures 2001 ·American Journal of Psychiatry ·Hower Kwon,Vinod Menon,Stéphan Eliez,Ilana S. Warsofsky,Christopher D. White,Jennifer Dyer-Friedman,Annette K. Taylor,Gary H. Glover,Allan L. Reiss	97
8	Discourse Processing in Women with Fragile X Syndrome: Evidence for a Deficit Establishing Coherence 2001 ·Cognitive Neuropsychology ·(unknown),Janice M. Keenan,Bruce F. Pennington,Annette K. Taylor,Randi J. Hagerman	32
9	Neurobehavioral phenotype in carriers of the fragile X premutation 2001 ·American Journal of Medical Genetics ·Cindy Johnston,Stéphan Eliez,Jennifer Dyer-Friedman,David Hessl,Bronwyn Glaser,Christine Blasey,Annette K. Taylor,Allan L. Reiss	96
10	A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1messenger RNA 2001 ·Journal of Medical Genetics ·Flora Tassone,Randi J. Hagerman,Annette K. Taylor,Paul J. Hagerman	60
11	Clinical involvement and protein expression in individuals with theFMR1 premutation 2000 ·American Journal of Medical Genetics ·Flora Tassone,Randi J. Hagerman,Annette K. Taylor,Janine B. Mills,Susan Harris,Louise W. Gane,Paul J. Hagerman	186
12	Functional brain activation during cognition is related to FMR1 gene expression 2000 ·Brain Research ·Vinod Menon,Hower Kwon,Stéphan Eliez,Annette K. Taylor,Allan L. Reiss	33
13	Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels ofFMR1 messenger RNA 2000 ·American Journal of Medical Genetics ·Flora Tassone,Randi J. Hagerman,Danuta Z. Loesch,Ave M. Lachiewicz,Annette K. Taylor,Paul J. Hagerman	120
14	Elevated Levels of FMR1 mRNA in Carrier Males: A New Mechanism of Involvement in the Fragile-X Syndromebreakdown → 2000 ·The American Journal of Human Genetics ·Flora Tassone,Randi J. Hagerman,Annette K. Taylor,Louise W. Gane,Tony E. Godfrey,Paul J. Hagerman	655
15	FMRP expression as a potential prognostic indicator in fragile X syndrome 1999 ·American Journal of Medical Genetics ·Flora Tassone,Randi J. Hagerman,(unknown),Pamela N. Dyer,(unknown),(unknown),Ben A. Oostra,Annette K. Taylor	259
16	Tissue‐specific methylation differences in a fragile X premutation carrier 1999 ·Clinical Genetics ·Flora Tassone,John Longshore,Janice Zunich,Peter Steinbach,(unknown),Annette K. Taylor	16
17	A controlled study of longitudinal IQ changes in females and males with fragile X syndrome 1996 ·American Journal of Medical Genetics ·(unknown),(unknown),Jeannette E. Riddle,Dennis W. Luckey,Annette K. Taylor,Randi J. Hagerman	47
18	Molecular/clinical correlations in females with fragile X 1996 ·American Journal of Medical Genetics ·William E. Sobesky,Annette K. Taylor,Bruce F. Pennington,Loisa Bennetto,(unknown),Jeannette E. Riddle,Randi J. Hagerman	71
19	High functioning fragile X males: Demonstration of an unmethylated fully expanded FMR‐1 mutation associated with protein expression 1994 ·American Journal of Medical Genetics ·Randi J. Hagerman,Claire Hull,(unknown),(unknown),Louise W. Staley,(unknown),(unknown),Michèle M. M. Mazzocco,Karen Snow,Stephen N. Thibodeau,(unknown),David L. Nelson,C. Thomas Caskey,Annette K. Taylor	176
20	Assignment of the human gene for CREB1 to chromosome 2q32.3–q34 1990 ·Genomics ·Annette K. Taylor,Ivana Klisak,T. Mohandas,Robert S. Sparkes,Ching Li,Richard B. Gaynor,Aldons J. Lusis	28

About Annette K. Taylor

Annette K. Taylor is a scholar working on Cognitive Neuroscience, Genetics and Gastroenterology, having authored 77 papers that have together received 5.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (54 papers), Autism Spectrum Disorder Research (38 papers) and Genomic variations and chromosomal abnormalities (17 papers). The work is most often cited by research in Cognitive Neuroscience (3.2k citations), Genetics (4.1k citations) and Molecular Biology (2.6k citations). Annette K. Taylor has collaborated with scholars based in United States, Australia and Sweden. Frequent co-authors include Randi J. Hagerman, Flora Tassone, Paul J. Hagerman, Louise W. Gane, Danuta Z. Loesch, Tony E. Godfrey, Richard Huggins, Minh Bui, Allan L. Reiss and Joseph B. Hellige. Their work appears in journals such as Science, Proceedings of the National Academy of Sciences and JAMA.

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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