Annette K. Taylor

7.0k total citations · 1 hit paper
77 papers, 5.5k citations indexed

About

Annette K. Taylor is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Annette K. Taylor has authored 77 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Genetics, 41 papers in Cognitive Neuroscience and 27 papers in Molecular Biology. Recurrent topics in Annette K. Taylor's work include Genetics and Neurodevelopmental Disorders (54 papers), Autism Spectrum Disorder Research (38 papers) and Genomic variations and chromosomal abnormalities (17 papers). Annette K. Taylor is often cited by papers focused on Genetics and Neurodevelopmental Disorders (54 papers), Autism Spectrum Disorder Research (38 papers) and Genomic variations and chromosomal abnormalities (17 papers). Annette K. Taylor collaborates with scholars based in United States, Australia and Sweden. Annette K. Taylor's 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 and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and JAMA.

In The Last Decade

Annette K. Taylor

76 papers receiving 5.3k citations

Hit Papers

1 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. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Annette K. Taylor United States	40	4.1k	3.2k	2.6k	340	311	77	5.5k
Danuta Z. Loesch Australia	40	4.1k 1.0×	2.3k 0.7×	2.2k 0.9×	219 0.6×	379 1.2×	164	5.4k
Jeanette J. A. Holden Canada	37	3.2k 0.8×	2.0k 0.6×	2.7k 1.0×	520 1.5×	724 2.3×	109	5.6k
Andrea Schneider United States	30	2.4k 0.6×	1.9k 0.6×	1.4k 0.5×	252 0.7×	339 1.1×	110	3.2k
Lauren A. Weiss United States	34	2.8k 0.7×	1.8k 0.6×	2.1k 0.8×	160 0.5×	365 1.2×	69	5.2k
Linda M. Brzustowicz United States	36	1.8k 0.4×	894 0.3×	2.3k 0.9×	432 1.3×	508 1.6×	91	4.5k
W. Ted Brown United States	31	2.5k 0.6×	1.6k 0.5×	1.5k 0.6×	130 0.4×	262 0.8×	97	3.4k
Jonathan Sebat United States	32	4.7k 1.1×	1.4k 0.4×	4.3k 1.7×	136 0.4×	570 1.8×	62	7.7k
Jonathan L. Haines United States	35	1.7k 0.4×	1.1k 0.3×	1.6k 0.6×	148 0.4×	469 1.5×	66	4.2k
Janine M. LaSalle United States	54	4.3k 1.0×	2.1k 0.7×	4.5k 1.7×	177 0.5×	348 1.1×	142	7.5k
Santhosh Girirajan United States	34	3.4k 0.8×	1.0k 0.3×	2.5k 1.0×	134 0.4×	399 1.3×	82	5.0k

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

Hicklin, R. Austin, et al.. (2025). Accuracy and reproducibility of latent print decisions on comparisons from searches of an automated fingerprint identification system. Forensic Science International. 370. 112457–112457. 1 indexed citations

Luzum, Jasmine A., Natasha Petry, Annette K. Taylor, et al.. (2021). Moving Pharmacogenetics Into Practice: It’s All About the Evidence!. Clinical Pharmacology & Therapeutics. 110(3). 649–661. 40 indexed citations

Crowley, James J., Jin Szatkiewicz, Anna K. Kähler, et al.. (2018). Common-variant associations with fragile X syndrome. Molecular Psychiatry. 24(3). 338–344. 6 indexed citations

Canetta, Pietro A., Annette K. Taylor, Carolina Argüelles-Grande, et al.. (2014). Lack of Serologic Evidence to Link IgA Nephropathy with Celiac Disease or Immune Reactivity to Gluten. PLoS ONE. 9(4). e94677–e94677. 25 indexed citations

Loesch, Danuta Z., Glynda Kinsella, F. Tassone, et al.. (2011). Fragile X‐associated tremor/ataxia phenotype in a male carrier of unmethylated full mutation in the FMR1 gene. Clinical Genetics. 82(1). 88–92. 56 indexed citations

Loesch, Danuta Z., Minh Bui, Cheryl Dissanayake, et al.. (2006). Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X. Neuroscience & Biobehavioral Reviews. 31(3). 315–326. 110 indexed citations

Loesch, Danuta Z., Richard Huggins, Minh Bui, et al.. (2003). Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis. American Journal of Medical Genetics Part A. 122A(1). 13–23. 48 indexed citations

Loesch, Danuta Z., Richard Huggins, Minh Bui, Annette K. Taylor, & Randi J. Hagerman. (2002). Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: A new perspective. American Journal of Medical Genetics Part A. 118A(2). 127–134. 36 indexed citations

Johnston, Cindy, Stéphan Eliez, Jennifer Dyer-Friedman, et al.. (2001). Neurobehavioral phenotype in carriers of the fragile X premutation. American Journal of Medical Genetics. 103(4). 314–319. 96 indexed citations

10.

Tassone, Flora, Randi J. Hagerman, Annette K. Taylor, & Paul J. Hagerman. (2001). A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1messenger RNA. Journal of Medical Genetics. 38(7). 453–456. 60 indexed citations

11.

Keenan, Janice M., et al.. (2001). Discourse Processing in Women with Fragile X Syndrome: Evidence for a Deficit Establishing Coherence. Cognitive Neuropsychology. 18(1). 1–18. 32 indexed citations

12.

Tassone, Flora, Randi J. Hagerman, Annette K. Taylor, et al.. (2000). Clinical involvement and protein expression in individuals with theFMR1 premutation. American Journal of Medical Genetics. 91(2). 144–152. 186 indexed citations

13.

Miller, Lucy, Daniel N. McIntosh, Annette K. Taylor, et al.. (1999). Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report. American Journal of Medical Genetics. 83(4). 268–279. 317 indexed citations

14.

Tassone, Flora, et al.. (1999). FMRP expression as a potential prognostic indicator in fragile X syndrome. American Journal of Medical Genetics. 84(3). 250–261. 259 indexed citations

15.

Tassone, Flora, et al.. (1999). Tissue‐specific methylation differences in a fragile X premutation carrier. Clinical Genetics. 55(5). 346–352. 16 indexed citations

16.

Riddle, Jeannette E., Amrita K. Cheema, William E. Sobesky, et al.. (1997). Phenotypic Involvement in Females With the FMR1 Gene Mutation. American Journal on Mental Retardation. 102(6). 590–590. 97 indexed citations

17.

Sobesky, William E., Annette K. Taylor, Bruce F. Pennington, et al.. (1996). Molecular/clinical correlations in females with fragile X. American Journal of Medical Genetics. 64(2). 340–345. 71 indexed citations

18.

Sobesky, William E., et al.. (1996). Molecular-clinical correlations in males with an expanded FMR1 mutation. American Journal of Medical Genetics. 64(2). 388–394. 163 indexed citations

19.

Hagerman, Randi J., Claire Hull, Louise W. Staley, et al.. (1994). High functioning fragile X males: Demonstration of an unmethylated fully expanded FMR‐1 mutation associated with protein expression. American Journal of Medical Genetics. 51(4). 298–308. 176 indexed citations

20.

Taylor, Annette K., Ivana Klisak, T. Mohandas, et al.. (1990). Assignment of the human gene for CREB1 to chromosome 2q32.3–q34. Genomics. 7(3). 416–421. 28 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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