Wendy L. Flejter

1.4k total citations
32 papers, 1.0k citations indexed

About

Wendy L. Flejter is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Wendy L. Flejter has authored 32 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 18 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Wendy L. Flejter's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Wendy L. Flejter is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Wendy L. Flejter collaborates with scholars based in United States, Lebanon and Germany. Wendy L. Flejter's co-authors include Jerome L. Gorski, Roger A. Schultz, Latisha McDaniel, E C Friedberg, Daniel L. Van Dyke, Stuart Schwartz, Joseph R. Testa, Marie McDonald, Susan Sheldon and Karen H. Antman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Cancer and The American Journal of Human Genetics.

In The Last Decade

Wendy L. Flejter

32 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wendy L. Flejter United States 15 547 542 157 132 125 32 1.0k
Heinz‐Ulrich G. Weier United States 17 712 1.3× 507 0.9× 174 1.1× 173 1.3× 153 1.2× 47 1.3k
Sandra Ruf Germany 14 1.1k 2.1× 397 0.7× 201 1.3× 113 0.9× 44 0.4× 20 1.8k
Karl Hackmann Germany 19 739 1.4× 614 1.1× 66 0.4× 110 0.8× 65 0.5× 54 1.3k
Udo Trautmann Germany 23 930 1.7× 1.1k 1.9× 331 2.1× 52 0.4× 328 2.6× 65 1.7k
Ayala Aviram‐Goldring Israel 17 411 0.8× 429 0.8× 73 0.5× 46 0.3× 244 2.0× 31 872
Beatrice Bodega Italy 17 1.6k 3.0× 351 0.6× 128 0.8× 165 1.3× 59 0.5× 32 2.3k
Jan Murken Germany 17 535 1.0× 633 1.2× 261 1.7× 62 0.5× 265 2.1× 51 1.1k
Ho-Lim Fung United States 11 1.4k 2.6× 262 0.5× 46 0.3× 93 0.7× 70 0.6× 11 1.6k
Tamar Golan‐Lev Israel 16 1.0k 1.9× 263 0.5× 57 0.4× 91 0.7× 76 0.6× 26 1.2k
Koichiro Nishino Japan 19 1.7k 3.1× 475 0.9× 48 0.3× 74 0.6× 117 0.9× 38 1.9k

Countries citing papers authored by Wendy L. Flejter

Since Specialization
Citations

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

Fields of papers citing papers by Wendy L. Flejter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wendy L. Flejter. 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 Wendy L. Flejter. The network helps show where Wendy L. Flejter may publish in the future.

Co-authorship network of co-authors of Wendy L. Flejter

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

All Works

20 of 20 papers shown
1.
2.
Flejter, Wendy L., et al.. (2017). Atypical ALK‐positive Spitz tumors with 9p21 homozygous deletion: Report of two cases and review of the literature. Journal of Cutaneous Pathology. 45(2). 136–140. 11 indexed citations
3.
Mirza, Fadi, Harshwardhan M. Thaker, Wendy L. Flejter, & Mary E. D’Alton. (2015). Fetomaternal Hemorrhage following Placement of an Intrauterine Pressure Catheter: Report of a New Association. Case Reports in Obstetrics and Gynecology. 2015. 1–3. 5 indexed citations
4.
Barber, Thomas A., Martin A. Schmidt, Ronald G. Tompkins, et al.. (2008). A microfluidics approach for the isolation of nucleated red blood cells (NRBCs) from the peripheral blood of pregnant women. Prenatal Diagnosis. 28(10). 892–899. 115 indexed citations
5.
Rao, P. Nagesh, et al.. (1999). Identification of the inverted chromosome 16 using chromosome painting. British Journal of Haematology. 104(3). 618–620. 3 indexed citations
6.
Rao, P. Nagesh, et al.. (1999). Identification of the inverted chromosome 16 using chromosome painting. British Journal of Haematology. 104(2). 201–201. 2 indexed citations
7.
Flejter, Wendy L., et al.. (1998). A Gene Involved in XY Sex Reversal Is Located on Chromosome 9, Distal to Marker D9S1779. The American Journal of Human Genetics. 63(3). 794–802. 75 indexed citations
8.
Flejter, Wendy L., et al.. (1998). Variegated aneuploidy in two siblings: Phenotype, genotype, CENP-E analysis, and literature review. American Journal of Medical Genetics. 75(1). 45–51. 12 indexed citations
9.
Flejter, Wendy L., Pamela E. Bennett‐Baker, Mohammad Ghaziuddin, et al.. (1996). Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation. American Journal of Medical Genetics. 61(2). 182–187. 67 indexed citations
10.
Flejter, Wendy L., Pamela E. Bennett‐Baker, Mohammad Ghaziuddin, et al.. (1996). Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation. American Journal of Medical Genetics. 61(2). 182–187. 5 indexed citations
11.
Flejter, Wendy L., et al.. (1996). Familial ring (19) chromosome mosaicism: Case report and review. American Journal of Medical Genetics. 66(3). 276–280. 10 indexed citations
12.
Zhang, Yifan, Wendy L. Flejter, M. Rivière, et al.. (1995). Localization of the human HTF4 transcription factors 4 gene (TCF12) to chromosome 15q21. Cytogenetic and Genome Research. 68(3-4). 235–238. 10 indexed citations
13.
Flejter, Wendy L., et al.. (1995). Region-specific cosmids and STRPs identified by chromosome microdissection and fish. Genomics. 25(2). 413–420. 4 indexed citations
14.
Abel, Kenneth J., Michael Boehnke, Peggy P. Ho, et al.. (1993). A Radiation Hybrid Map of the BRCA1 Region of Chromosome 17q12-q21. Genomics. 17(3). 632–641. 34 indexed citations
15.
Flejter, Wendy L., et al.. (1993). Tetranucleotide repeat polymorphism at D17S846 maps within 40 kb of GAS at 17q12–q22. Human Molecular Genetics. 2(7). 1080–1080. 10 indexed citations
16.
Flejter, Wendy L., Eric D. Lynch, Michael Boehnke, et al.. (1993). Multicolor FISH Mapping with Alu-PCR-Amplified YAC Clone DNA Determines the Order of Markers in the BRCA1 Region on Chromosome 17q12-q21. Genomics. 17(3). 624–631. 18 indexed citations
17.
Graziano, Stephen L., Andrea M. A. Pfeifer, Joseph R. Testa, et al.. (1991). Involvement of the RAFI locus, at band 3p25, in the 3p deletion of small‐cell lung cancer. Genes Chromosomes and Cancer. 3(4). 283–293. 29 indexed citations
18.
Flejter, Wendy L., Jacqueline Astemborski, Thomas Hassel, & Maimon M. Cohen. (1989). Cytogenetic Effects of Phenytoin and/or Carbamazepine on Human Peripheral Leukocytes. Epilepsia. 30(3). 374–379. 9 indexed citations
19.
Flejter, Wendy L., Frederick P. Li, Karen H. Antman, & Joseph R. Testa. (1989). Recurring loss involving chromosomes 1, 3, and 22 in malignant mesothelioma: Possible sites of tumor suppressor genes. Genes Chromosomes and Cancer. 1(2). 148–154. 78 indexed citations
20.
Flejter, Wendy L., Daniel L. Van Dyke, & Lester Weiss. (1986). Location of the X inactivation center in primates and other mammals. Human Genetics. 74(1). 63–66. 4 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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