Anne E. Wiktor

2.2k total citations
55 papers, 1.5k citations indexed

About

Anne E. Wiktor is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Anne E. Wiktor has authored 55 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 16 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Anne E. Wiktor's work include Genomic variations and chromosomal abnormalities (17 papers), Acute Myeloid Leukemia Research (10 papers) and Prenatal Screening and Diagnostics (10 papers). Anne E. Wiktor is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Acute Myeloid Leukemia Research (10 papers) and Prenatal Screening and Diagnostics (10 papers). Anne E. Wiktor collaborates with scholars based in United States, Belgium and Poland. Anne E. Wiktor's co-authors include Daniel L. Van Dyke, William R. Sukov, Robert B. Jenkins, Rhett P. Ketterling, Koichi Maeda, Benjamin A. Rybicki, Lester Weiss, Kathryn E. Pearce, Jennelle C. Hodge and Christopher A. Sattler and has published in prestigious journals such as Journal of Clinical Oncology, Blood and Cancer.

In The Last Decade

Anne E. Wiktor

54 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne E. Wiktor United States 22 547 415 410 401 263 55 1.5k
Julian D. Down United States 23 532 1.0× 295 0.7× 164 0.4× 471 1.2× 569 2.2× 50 2.0k
Rosalyn Slater Netherlands 28 1.4k 2.6× 478 1.2× 493 1.2× 207 0.5× 436 1.7× 69 2.4k
C.A. Griffin United States 21 795 1.5× 419 1.0× 267 0.7× 390 1.0× 619 2.4× 41 2.1k
António E. Pinto Portugal 24 707 1.3× 742 1.8× 399 1.0× 149 0.4× 660 2.5× 74 2.4k
Sabine Strehl Austria 31 1.1k 2.1× 437 1.1× 263 0.6× 788 2.0× 825 3.1× 72 2.9k
W. F. Benedict United States 9 998 1.8× 828 2.0× 416 1.0× 186 0.5× 155 0.6× 11 1.9k
W. Grote Germany 23 440 0.8× 529 1.3× 251 0.6× 141 0.4× 196 0.7× 98 1.8k
Nancy R. Schneider United States 21 581 1.1× 364 0.9× 267 0.7× 233 0.6× 236 0.9× 49 1.4k
Carol Berger United States 22 831 1.5× 296 0.7× 530 1.3× 308 0.8× 99 0.4× 43 1.6k
Olivier Caron France 23 1.0k 1.9× 842 2.0× 721 1.8× 268 0.7× 68 0.3× 72 2.4k

Countries citing papers authored by Anne E. Wiktor

Since Specialization
Citations

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

Fields of papers citing papers by Anne E. Wiktor

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anne E. Wiktor. 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 Anne E. Wiktor. The network helps show where Anne E. Wiktor may publish in the future.

Co-authorship network of co-authors of Anne E. Wiktor

This figure shows the co-authorship network connecting the top 25 collaborators of Anne E. Wiktor. A scholar is included among the top collaborators of Anne E. Wiktor 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 Anne E. Wiktor. Anne E. Wiktor 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.
Yoon, Harry H., Mark A. Lewis, Nathan R. Foster, et al.. (2016). Central nervous system relapse in patients with untreated HER2‐positive esophageal or gastroesophageal junction adenocarcinoma. International Journal of Cancer. 139(7). 1626–1631. 10 indexed citations
3.
4.
Aypar, Umut, Ryan A. Knudson, Kathryn E. Pearce, Anne E. Wiktor, & Rhett P. Ketterling. (2014). Development of an NPM1/MLF1 D-FISH Probe Set for the Detection of t(3;5)(q25;q35) Identified in Patients with Acute Myeloid Leukemia. Journal of Molecular Diagnostics. 16(5). 527–532. 7 indexed citations
5.
Yoon, Harry H., Qian Shi, William R. Sukov, et al.. (2012). Association of HER2/ErbB2 Expression and Gene Amplification with Pathologic Features and Prognosis in Esophageal Adenocarcinomas. Clinical Cancer Research. 18(2). 546–554. 116 indexed citations
6.
Sukov, William R., Jennelle C. Hodge, Christine M. Lohse, et al.. (2012). TFE3 Rearrangements in Adult Renal Cell Carcinoma. The American Journal of Surgical Pathology. 36(5). 663–670. 118 indexed citations
7.
Wiktor, Anne E., Daniel L. Van Dyke, Janice M. Hodnefield, Jeanette E. Eckel‐Passow, & Curtis A. Hanson. (2011). The significance of isolated Y chromosome loss in bone marrow metaphase cells from males over age 50 years. Leukemia Research. 35(10). 1297–1300. 19 indexed citations
8.
Wiktor, Anne E., et al.. (2009). Identification of sex chromosome mosaicism: Is analysis of 20 metaphase cells sufficient?. American Journal of Medical Genetics Part A. 149A(2). 257–259. 4 indexed citations
9.
Dewald, Gordon W., Thomas C. Smyrk, Erik C. Thorland, et al.. (2009). Fluorescence In Situ Hybridization to Visualize Genetic Abnormalities in Interphase Cells of Acinar Cell Carcinoma, Ductal Adenocarcinoma, and Islet Cell Carcinoma of the Pancreas. Mayo Clinic Proceedings. 84(9). 801–810. 23 indexed citations
10.
Thorland, Erik C., Patrick R. Gonzales, Troy J. Gliem, Anne E. Wiktor, & Rhett P. Ketterling. (2007). Comprehensive validation of array comparative genomic hybridization platforms: how much is enough?. Genetics in Medicine. 9(9). 632–641. 8 indexed citations
11.
Welch, Robert, et al.. (2006). Operator experience and sample quality in genetic amniocentesis. American Journal of Obstetrics and Gynecology. 194(1). 189–191. 22 indexed citations
12.
Wiktor, Anne E. & Daniel L. Van Dyke. (2004). FISH analysis helps identify low-level mosaicism in Ullrich-Turner syndrome patients. Genetics in Medicine. 6(3). 132–135. 19 indexed citations
13.
Zhang, Yanming, Jianjun Chen, Muhammad Shurafa, et al.. (2004). PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22). Genes Chromosomes and Cancer. 40(4). 365–370. 31 indexed citations
14.
Asamoah, Alexander, et al.. (2003). Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay. American Journal of Medical Genetics Part A. 118A(1). 82–85. 4 indexed citations
15.
Monaghan, Kristin G., Anne E. Wiktor, & Daniel L. Van Dyke. (2002). Diagnostic testing for Prader-Willi syndrome and Angelman syndrome: A cost comparison. Genetics in Medicine. 4(6). 448–450. 9 indexed citations
16.
Roberson, Jacquelyn, et al.. (2001). Prenatal diagnosis of 22q11.2 deletion when ultrasound examination reveals a heart defect. Genetics in Medicine. 3(1). 65–66. 17 indexed citations
17.
Wiktor, Anne E., et al.. (2001). Deletion of 2q37 and duplication of 10q24: Two cases in the same family and review of the literature. Annales de Génétique. 44(3). 129–134. 3 indexed citations
18.
Wiktor, Anne E., et al.. (1994). 10p Duplication characterized by fluorescence in situ hybridization. American Journal of Medical Genetics. 52(3). 315–318. 8 indexed citations
19.
Wiktor, Anne E., et al.. (1993). X‐inactivation pattern in an Ullrich–Turner syndrome patient with a small ring X and normal intelligence. American Journal of Medical Genetics. 47(4). 490–493. 9 indexed citations
20.
Dyke, Daniel L. Van, Anne E. Wiktor, Dorothy A. Miller, et al.. (1992). Ullrich‐Turner syndrome with a small ring X chromosome and presence of mental retardation. American Journal of Medical Genetics. 43(6). 996–1005. 72 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Julian D. Down Breakdown of academic impact, for papers by Rosalyn Slater Breakdown of academic impact, for papers by C.A. Griffin Breakdown of academic impact, for papers by António E. Pinto Breakdown of academic impact, for papers by Sabine Strehl Breakdown of academic impact, for papers by W. F. Benedict Breakdown of academic impact, for papers by W. Grote Breakdown of academic impact, for papers by Nancy R. Schneider Breakdown of academic impact, for papers by Carol Berger Breakdown of academic impact, for papers by Olivier Caron
Rankless by CCL
2026