H.E. Wyandt

512 total citations
25 papers, 405 citations indexed

About

H.E. Wyandt is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, H.E. Wyandt has authored 25 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in H.E. Wyandt's work include Genomic variations and chromosomal abnormalities (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). H.E. Wyandt is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). H.E. Wyandt collaborates with scholars based in United States. H.E. Wyandt's co-authors include Aubrey Milunsky, Frederick Hecht, James Skare, Thaddeus E. Kelly, Angela E. Lin, Bassem R. Haddad, Robert F. Troxler, Ruth Anderson, FG Oppenheim and Vanessa M. Barnabei and has published in prestigious journals such as Science, New England Journal of Medicine and The American Journal of Human Genetics.

In The Last Decade

H.E. Wyandt

24 papers receiving 382 citations

Peers

H.E. Wyandt

GENET

PPCH

ONCOL

E.M. Dauber Austria

Nadja Kokalj-Vokač Slovenia

A. Caine United Kingdom

Sugandhi A. Tharapel United States

J. W. Siebers Germany

Jody L. Lerner United States

Lynne S. Rosenblum‐Vos United States

Barbara Ruben Migeon United States

Shannon E. Duke United States

Zhanhe Wu Australia

E.M. Dauber Austria

H.E. Wyandt

211 ×0.8

GENET

150 ×0.7

16 ×0.2

63 ×0.7

PPCH

10 ×0.2

ONCOL

Citations per year, relative to H.E. Wyandt H.E. Wyandt (= 1×) peers E.M. Dauber

Countries citing papers authored by H.E. Wyandt

Since Specialization

Citations

This map shows the geographic impact of H.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 H.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 H.E. Wyandt more than expected).

Fields of papers citing papers by H.E. Wyandt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Pan, An, et al.. (2003). FISH Variants with D15Z1.. PubMed. 29(4). 146–151. 5 indexed citations

Haddad, Bassem R., Angela E. Lin, H.E. Wyandt, & Aubrey Milunsky. (1996). Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).. Journal of Medical Genetics. 33(12). 1045–1047. 45 indexed citations

Wyandt, H.E., et al.. (1994). Interstitial telomeric sequences in human chromosomes cluster with common fragile sites, mutagen sensitive sites, viral integration sites, cancer breakpoints, proto-oncogenes and breakpoints involved in primate evolution. The American Journal of Human Genetics. 55. 1 indexed citations

Mark, Hon Fong L., et al.. (1993). A study of homologous chromosomes using a morphometric approach. Genome. 36(5). 1003–1006. 3 indexed citations

Milunsky, Aubrey, et al.. (1993). 46,XY/47,XYY male with the fragile X syndrome: Cytogenetic and molecular studies. American Journal of Medical Genetics. 45(5). 589–593. 5 indexed citations

Troxler, Robert F., Gwynneth D. Offner, Bai‐Lin Wu, et al.. (1993). Localization of the gene for human heart fatty acid binding protein to chromosome 1p32-1p33. Human Genetics. 92(6). 563–566. 14 indexed citations

Tonk, Vijay S., et al.. (1992). Abnormalities of chromosome 22 in meningiomas and confirmation of the origin of a dicentric 22 by in situ hybridization. Cancer Genetics and Cytogenetics. 64(1). 65–68. 11 indexed citations

Wyandt, H.E., et al.. (1992). Cytogenetic studies of an adrenal cortical carcinoma. Cancer Genetics and Cytogenetics. 61(1). 96–98. 5 indexed citations

Wyandt, H.E., H L Grierson, Warren G. Sanger, et al.. (1989). Chromosome deletion of Xq25 in an individual with X‐linked lymphoproliferative disease. American Journal of Medical Genetics. 33(3). 426–430. 30 indexed citations

10.

vanderSpek, Johanna C., H.E. Wyandt, James Skare, et al.. (1989). Localization of the genes for histatins to human chromosome 4q13 and tissue distribution of the mRNAs.. PubMed. 45(3). 381–7. 48 indexed citations

11.

Kelly, Thaddeus E., et al.. (1986). Secondary amenorrhoea and 47,XX,i(Xq) karyotype.. Journal of Medical Genetics. 23(4). 371.3–372. 3 indexed citations

12.

Barnabei, Vanessa M., et al.. (1983). Isodicentric X Chromosome in a Girl With Gonadal Dysgenesis. Southern Medical Journal. 76(2). 249–250. 6 indexed citations

13.

Wyandt, H.E., et al.. (1982). Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchange. Cytogenetic and Genome Research. 33(3). 222–231. 19 indexed citations

14.

Wyandt, H.E., et al.. (1980). Interstitial 3p deletion in a child due to paternal paracentric inserted inversion.. PubMed. 32(5). 731–5. 40 indexed citations

15.

Wyandt, H.E., et al.. (1980). Mechanisms of Giemsa banding. Human Genetics. 53(2). 1 indexed citations

16.

Wyandt, H.E., et al.. (1978). Giemsa-11 Staining of Chromosome 1: A Newly Described Heteromorphism. Science. 202(4363). 64–65. 23 indexed citations

17.

Wyandt, H.E., et al.. (1976). Mechanisms of Giemsa banding of chromosomes. Experimental Cell Research. 102(1). 85–94. 43 indexed citations

18.

Prescott, Gerald H., et al.. (1973). Restrictive Consent and Amniocentesis. New England Journal of Medicine. 288(19). 1028–1028.

19.

Wyandt, H.E., et al.. (1973). Human Y-chromatin. Experimental Cell Research. 81(2). 468–473. 20 indexed citations

20.

Wyandt, H.E. & Frederick Hecht. (1973). Human Y-chromatin. Experimental Cell Research. 81(2). 453–461. 8 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