Hope H. Punnett

3.1k total citations
66 papers, 2.2k citations indexed

About

Hope H. Punnett is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hope H. Punnett has authored 66 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 27 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hope H. Punnett's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). Hope H. Punnett is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). Hope H. Punnett collaborates with scholars based in United States, United Kingdom and Canada. Hope H. Punnett's co-authors include Mildred L. Kistenmacher, Judy Fletcher, Veronica van Heyningen, Rebecca Adams, Isabel M. Hanson, Alison Brown, Tim Jordan, David Taylor, Harold W. Lischner and Elaine H. Zackai and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

Hope H. Punnett

63 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hope H. Punnett United States 25 1.2k 967 326 262 205 66 2.2k
Umadevi Tantravahi United States 29 1.4k 1.1× 946 1.0× 416 1.3× 237 0.9× 281 1.4× 67 2.7k
Tatsuro Ikeuchi Japan 28 1.4k 1.1× 869 0.9× 271 0.8× 340 1.3× 370 1.8× 106 2.6k
Loris McGavran United States 24 1.2k 0.9× 670 0.7× 165 0.5× 427 1.6× 185 0.9× 61 2.7k
Jay W. Ellison United States 23 1.2k 1.0× 1.2k 1.3× 438 1.3× 249 1.0× 210 1.0× 52 2.6k
Syed M. Jalal United States 28 1.3k 1.1× 1.0k 1.0× 314 1.0× 253 1.0× 348 1.7× 71 2.6k
Janet M. Cowan United States 25 1.1k 0.9× 553 0.6× 452 1.4× 233 0.9× 134 0.7× 56 2.0k
Susan Pfeifer‐Ohlsson Sweden 16 1.1k 0.9× 519 0.5× 287 0.9× 94 0.4× 94 0.5× 23 1.6k
Shirley Soukup United States 23 774 0.6× 556 0.6× 304 0.9× 366 1.4× 197 1.0× 66 1.7k
Samia A. Temtamy Egypt 29 1.4k 1.1× 1.6k 1.7× 288 0.9× 168 0.6× 82 0.4× 127 2.9k
Lester Weiss United States 29 918 0.7× 1.4k 1.4× 448 1.4× 102 0.4× 416 2.0× 82 2.3k

Countries citing papers authored by Hope H. Punnett

Since Specialization
Citations

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

Fields of papers citing papers by Hope H. Punnett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hope H. Punnett

This figure shows the co-authorship network connecting the top 25 collaborators of Hope H. Punnett. A scholar is included among the top collaborators of Hope H. Punnett 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 Hope H. Punnett. Hope H. Punnett 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.
Anderson, Carol E., et al.. (2014). Co‐occurrence of non‐mosaic trisomy 22 and inherited balanced t(4;6)(q33;q23.3) in a liveborn female: Case report and review of the literature. American Journal of Medical Genetics Part A. 164(12). 3187–3193. 7 indexed citations
2.
Morrissette, Jennifer J.D., et al.. (2006). Down syndrome with low hypodiploidy in precursor B-cell acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 169(1). 58–61. 2 indexed citations
3.
Cushman, Lisa J., Wilfredo Torres‐Martinez, Athena M. Cherry, et al.. (2005). A report of three patients with an interstitial deletion of chromosome 15q24. American Journal of Medical Genetics Part A. 137A(1). 65–71. 27 indexed citations
4.
Punnett, Hope H., et al.. (2004). Translocation (16;18)(p13;q21.3) in follicular lymphoma. Cancer Genetics and Cytogenetics. 154(2). 160–162. 2 indexed citations
5.
Han, Xiang Y., Daniel Conway, Bruce Pawel, et al.. (2000). Truncus arteriosus and other lethal internal anomalies in Goltz syndrome. American Journal of Medical Genetics. 90(1). 45–45. 1 indexed citations
6.
Davidson, Alexander, Meena Khandelwal, & Hope H. Punnett. (1997). PRENATAL DIAGNOSIS OF THE 22q11 DELETION SYNDROME. Prenatal Diagnosis. 17(4). 380–383. 15 indexed citations
7.
Hughes-Benzie, R, Giuseppe Pilia, Alasdair G. W. Hunter, et al.. (1996). Simpson-Golabi-Behmel syndrome: Genotype/phenotype analysis of 18 affected males from 7 unrelated families. American Journal of Medical Genetics. 66(2). 227–234. 109 indexed citations
8.
Chadarévian, Jean‐Pierre de, et al.. (1996). Hyperdiploidy and trisomy 12 in the cystic partially differentiated nephroblastoma. Human Pathology. 27(9). 980–981. 9 indexed citations
9.
Shkolny, Dana L., Terry R. Brown, Hope H. Punnett, et al.. (1995). Characterization of alternative amino acid substitutions at arginine 830 of the androgen receptor that cause complete androgen insensitivity in three families. Human Molecular Genetics. 4(4). 515–521. 9 indexed citations
10.
Hanson, Isabel M., Judy Fletcher, Tim Jordan, et al.. (1994). Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly. Nature Genetics. 6(2). 168–173. 381 indexed citations
11.
Punnett, Hope H., et al.. (1994). Cytogenetic analysis of a choroid plexus papilloma. Genes Chromosomes and Cancer. 10(4). 282–285. 14 indexed citations
12.
Bergoffen, JoAnn, et al.. (1993). Diaphragmatic hernia in tetrasomy 12p mosaicism. The Journal of Pediatrics. 122(4). 603–606. 35 indexed citations
13.
Punnett, Hope H., et al.. (1989). Translocation 10;17 in clear cell sarcoma of the kidney. Cancer Genetics and Cytogenetics. 41(1). 123–128. 48 indexed citations
14.
Gorski, Jerome L., Mildred L. Kistenmacher, Hope H. Punnett, et al.. (1988). Reproductive risks for carriers of complex chromosome rearrangements: Analysis of 25 families. American Journal of Medical Genetics. 29(2). 247–261. 83 indexed citations
15.
Punnett, Hope H., et al.. (1985). Carrier detection in cystic fibrosis. The Journal of Pediatrics. 106(6). 913–917. 2 indexed citations
16.
Kelley, Richard I., Elaine H. Zackai, Beverly S. Emanuel, et al.. (1982). The association of the DiGeorge anomalad with partial monosomy of chromosome 22. The Journal of Pediatrics. 101(2). 197–200. 145 indexed citations
17.
Blattner, William A., et al.. (1980). Clinical manifestations of familial 13;18 translocation.. Journal of Medical Genetics. 17(5). 373–379. 12 indexed citations
18.
León, Guillermo A. de, et al.. (1977). Globoid cells, glial nodules, and peculiar fibrillary changes in the cerebro‐hepato‐renal syndrome of zellweger. Annals of Neurology. 2(6). 473–484. 35 indexed citations
19.
Punnett, Hope H. & John A. Kirkpatrick. (1968). A syndrome of ocular abnormalities, calcification of cartilage, and failure to thrive. The Journal of Pediatrics. 73(4). 602–606. 23 indexed citations
20.
Punnett, Hope H., et al.. (1964). Serial cytogenetic and hematologic studies on amongol with trisomy-21 and acute congenital leukemia. The Journal of Pediatrics. 65(6). 880–887. 57 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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