Lisa F. Taft

2.3k total citations
13 papers, 1.6k citations indexed

About

Lisa F. Taft is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience. According to data from OpenAlex, Lisa F. Taft has authored 13 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 4 papers in Cognitive Neuroscience. Recurrent topics in Lisa F. Taft's work include Prenatal Screening and Diagnostics (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Lisa F. Taft is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Lisa F. Taft collaborates with scholars based in United States, Denmark and Greece. Lisa F. Taft's co-authors include Stephanie L. Sherman, Terry Hassold, Sallie B. Freeman, Muin J. Khoury, Dorothy Pettay, Michael B. Petersen, Margareta Mikkelsen, Kenneth J. Dooley, Quanhe Yang and James L. Newman and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Lisa F. Taft

12 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lisa F. Taft United States	12	689	580	553	418	305	13	1.6k
Décio Brunoni Brazil	23	555 0.8×	413 0.7×	482 0.9×	298 0.7×	68 0.2×	98	1.8k
Leslie A. O’Leary United States	17	401 0.6×	416 0.7×	580 1.0×	183 0.4×	375 1.2×	25	1.5k
Juan Clinton Llerena Brazil	23	601 0.9×	346 0.6×	400 0.7×	237 0.6×	143 0.5×	112	1.6k
Elizabeth McPherson United States	25	748 1.1×	495 0.9×	565 1.0×	128 0.3×	94 0.3×	85	1.5k
Arabella Smith Australia	22	1.2k 1.7×	591 1.0×	605 1.1×	132 0.3×	46 0.2×	119	1.8k
Margaret P Adam United States	26	694 1.0×	1.6k 2.8×	644 1.2×	376 0.9×	141 0.5×	82	2.8k
Cheryl Shuman Canada	28	1.6k 2.3×	1.1k 1.9×	1.2k 2.2×	213 0.5×	63 0.2×	70	2.4k
Stuart W. Tinker United States	15	298 0.4×	302 0.5×	283 0.5×	209 0.5×	190 0.6×	15	776
E.J.T. Winsor Canada	20	450 0.7×	596 1.0×	283 0.5×	107 0.3×	129 0.4×	46	1.2k
Kristin M. May United States	13	461 0.7×	359 0.6×	674 1.2×	38 0.1×	315 1.0×	18	1.2k

Countries citing papers authored by Lisa F. Taft

Since Specialization

Citations

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

Fields of papers citing papers by Lisa F. Taft

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lisa F. Taft. 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 Lisa F. Taft. The network helps show where Lisa F. Taft may publish in the future.

Co-authorship network of co-authors of Lisa F. Taft

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

All Works

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13 of 13 papers shown

Anido, Aimee, Lisa M. Carlson, Lisa F. Taft, & Stephanie L. Sherman. (2005). Women’s Attitudes Toward Testing for Fragile X Carrier Status: A Qualitative Analysis. Journal of Genetic Counseling. 14(4). 295–306.

Anido, Aimee, Lisa M. Carlson, Lisa F. Taft, & Stephanie L. Sherman. (2005). Women's Attitudes Toward Testing for Fragile X Carrier Status: A Qualitative Analysis. Journal of Genetic Counseling. 14(4). 295–306. 33 indexed citations

Crawford, Dana C., Kellen L. Meadows, James L. Newman, et al.. (2002). Prevalence of the fragile X syndrome in African‐Americans. American Journal of Medical Genetics. 110(3). 226–233. 113 indexed citations

Crawford, Dana C., Charles E. Schwartz, Kellen L. Meadows, et al.. (2000). Survey of the Fragile X Syndrome CGG Repeat and the Short-Tandem-Repeat and Single-Nucleotide-Polymorphism Haplotypes in an African American Population. The American Journal of Human Genetics. 66(2). 480–493. 44 indexed citations

Freeman, Sallie B., et al.. (2000). Women with a Reduced Ovarian Complement May Have an Increased Risk for a Child with Down Syndrome. The American Journal of Human Genetics. 66(5). 1680–1683. 92 indexed citations

Crawford, Dana C., Kellen L. Meadows, James L. Newman, et al.. (1999). Prevalence and Phenotype Consequence of FRAXA and FRAXE Alleles in a Large, Ethnically Diverse, Special Education–Needs Population. The American Journal of Human Genetics. 64(2). 495–507. 99 indexed citations

Yang, Quanhe, Stephanie L. Sherman, Terry Hassold, et al.. (1999). Risk factors for trisomy 21: Maternal cigarette smoking and oral contraceptive use in a spopulation-based case-control study. Genetics in Medicine. 1(3). 80–88. 71 indexed citations

Hixon, Mary L., et al.. (1998). FISH studies of the sperm of fathers of paternally derived cases of trisomy 21: no evidence for an increase in aneuploidy. Human Genetics. 103(6). 654–657. 28 indexed citations

Freeman, Sallie B., Lisa F. Taft, Kenneth J. Dooley, et al.. (1998). Population‐based study of congenital heart defects in Down syndrome. American Journal of Medical Genetics. 80(3). 213–217. 237 indexed citations

10.

Taft, Lisa F., et al.. (1998). Population-based study of congenital heart defects in Down syndrome. American Journal of Medical Genetics. 80(3). 213–217. 279 indexed citations

11.

Yoon, Paula W., Sallie B. Freeman, S. L. Sherman, et al.. (1996). Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.. PubMed. 58(3). 628–33. 145 indexed citations

12.

Lamb, Neil E., Sallie B. Freeman, Dorothy Pettay, et al.. (1996). Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II. Nature Genetics. 14(4). 400–405. 290 indexed citations

13.

Sherman, Stephanie L., Michael B. Petersen, Sallie B. Freeman, et al.. (1994). Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination. Human Molecular Genetics. 3(9). 1529–1535. 141 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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