Herman E. Wyandt

782 total citations
40 papers, 517 citations indexed

About

Herman E. Wyandt is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, Herman E. Wyandt has authored 40 papers receiving a total of 517 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 17 papers in Pediatrics, Perinatology and Child Health and 15 papers in Plant Science. Recurrent topics in Herman E. Wyandt's work include Genomic variations and chromosomal abnormalities (26 papers), Prenatal Screening and Diagnostics (16 papers) and Chromosomal and Genetic Variations (15 papers). Herman E. Wyandt is often cited by papers focused on Genomic variations and chromosomal abnormalities (26 papers), Prenatal Screening and Diagnostics (16 papers) and Chromosomal and Genetic Variations (15 papers). Herman E. Wyandt collaborates with scholars based in United States, France and Canada. Herman E. Wyandt's co-authors include Aubrey Milunsky, Vijay S. Tonk, Jeff M. Milunsky, Aubrey Milunsky, James Skare, Thaddeus E. Kelly, J. Andrew Carlson, James F. Reynolds, Xinli Huang and Helen L. Grierson and has published in prestigious journals such as Nature, New England Journal of Medicine and Genomics.

In The Last Decade

Herman E. Wyandt

40 papers receiving 500 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Herman E. Wyandt United States 15 359 205 169 108 50 40 517
E. Orye Belgium 14 311 0.9× 233 1.1× 137 0.8× 122 1.1× 65 1.3× 35 590
Judith Dagan Israel 12 223 0.6× 231 1.1× 96 0.6× 88 0.8× 39 0.8× 27 457
Philippe Coullin France 15 208 0.6× 268 1.3× 189 1.1× 76 0.7× 23 0.5× 28 526
Chansonette Harvard Canada 17 417 1.2× 294 1.4× 185 1.1× 85 0.8× 53 1.1× 19 681
Michael J. Macera United States 13 193 0.5× 165 0.8× 76 0.4× 130 1.2× 31 0.6× 43 400
M.M. Aronson United States 13 213 0.6× 264 1.3× 90 0.5× 83 0.8× 45 0.9× 48 498
Stephen Laderman United States 4 541 1.5× 436 2.1× 126 0.7× 211 2.0× 31 0.6× 4 783
Ernest Lieber United States 10 312 0.9× 230 1.1× 178 1.1× 79 0.7× 45 0.9× 24 581
Atsuko Fujimoto United States 19 489 1.4× 310 1.5× 267 1.6× 153 1.4× 42 0.8× 45 868
Fiorella Shabtai Israel 17 314 0.9× 229 1.1× 63 0.4× 109 1.0× 63 1.3× 47 601

Countries citing papers authored by Herman E. Wyandt

Since Specialization
Citations

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

Fields of papers citing papers by Herman E. Wyandt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Herman E. Wyandt

This figure shows the co-authorship network connecting the top 25 collaborators of Herman E. Wyandt. A scholar is included among the top collaborators of Herman E. Wyandt 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 Herman E. Wyandt. Herman E. Wyandt 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.
Wyandt, Herman E., et al.. (2006). Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH. Experimental and Molecular Pathology. 80(3). 262–266. 6 indexed citations
2.
Mark, Hon Fong L., et al.. (2005). Constitutional partial 1q trisomy mosaicism and Wilms tumor. Cancer Genetics and Cytogenetics. 162(2). 166–171. 7 indexed citations
3.
Tonk, Vijay S., Golder N. Wilson, Robert C. Schutt, et al.. (2005). Costovertebral dysplasia in a patient with partial trisomy 22. Experimental and Molecular Pathology. 80(2). 197–200. 1 indexed citations
4.
Wyandt, Herman E. & Vijay S. Tonk. (2004). Atlas of Human Chromosome Heteromorphisms. 35 indexed citations
5.
Prabhakara, Karthik S., et al.. (2004). Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18. Annales de Génétique. 47(3). 297–303. 6 indexed citations
6.
Wyandt, Herman E.. (2001). In Memoriam: Dr. Ram Verma, Cytogeneticist, Passes Away. Annales de Génétique. 44(2). 111–111. 1 indexed citations
7.
Chinnappan, Dharmaraj, et al.. (2001). Acquired Robertsonian translocations in two leukemia patients. Cancer Genetics and Cytogenetics. 131(2). 104–108. 3 indexed citations
8.
Wyandt, Herman E., et al.. (2000). Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy. American Journal of Medical Genetics. 93(4). 305–312. 1 indexed citations
9.
Milunsky, Jeff M., et al.. (1999). Schizophrenia susceptibility gene locus at Xp22.3. Clinical Genetics. 55(6). 455–460. 42 indexed citations
10.
Chinnappan, Dharmaraj, Janet M. Cowan, Archana Rastogi, et al.. (1998). Discrepant Cytogenetic and Fluorescence In Situ Hybridization Results in a 26-Year-Old Male with Early T-Cell Acute Lymphocytic Leukemia. Cancer Genetics and Cytogenetics. 106(2). 116–121. 2 indexed citations
11.
Wyandt, Herman E., et al.. (1998). Fluorescence In Situ Hybridization to Assess Aneuploidy for Chromosomes 7 and 8 in Hematologic Disorders. Cancer Genetics and Cytogenetics. 102(2). 114–124. 20 indexed citations
12.
Wyandt, Herman E., et al.. (1996). Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant. American Journal of Medical Genetics. 61(3). 269–273. 4 indexed citations
13.
Wyandt, Herman E., et al.. (1996). Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant. American Journal of Medical Genetics. 61(3). 269–273. 25 indexed citations
14.
Estabrooks, Laurel L., W. Roy Breg, Michael R. Hayden, et al.. (1995). Summary of the 1993 ASHG ancillary meeting “recent research on chromosome 4p syndromes and genes”. American Journal of Medical Genetics. 55(4). 453–458. 21 indexed citations
15.
Carlson, J. Andrew, et al.. (1992). Cytogenetic studies of eight squamous cell carcinomas of the head and neck. Cancer Genetics and Cytogenetics. 59(1). 73–78. 30 indexed citations
16.
Wyandt, Herman E., et al.. (1991). Report of a variant t(1;15;17)(p36;q22;q21.1) in a patient with acute promyelocytic leukemia. Cancer Genetics and Cytogenetics. 57(2). 201–207. 20 indexed citations
17.
Sanger, Warren G., Helen L. Grierson, James Skare, et al.. (1990). Partial Xq25 deletion in a family with the X-linked lymphoproliferative disease (XLP). Cancer Genetics and Cytogenetics. 47(2). 163–169. 29 indexed citations
18.
Wyandt, Herman E., et al.. (1989). Emerging phenotype of duplication (7p): A report of three cases and review of the literature. American Journal of Medical Genetics. 33(3). 364–368. 26 indexed citations
19.
Reynolds, James F., et al.. (1985). De novo 21q interstitial deletion in a retarded boy with ulno‐fibular dysostosis. American Journal of Medical Genetics. 20(1). 173–180. 23 indexed citations
20.
Wyandt, Herman E., et al.. (1973). Quinacrine studies of sex chromatin and nucleoli in human Brain. PubMed. 20(4). 329–333. 3 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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