Heidi Whitby

827 total citations
7 papers, 180 citations indexed

About

Heidi Whitby is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Heidi Whitby has authored 7 papers receiving a total of 180 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Plant Science and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Heidi Whitby's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Rare Diseases (3 papers). Heidi Whitby is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Rare Diseases (3 papers). Heidi Whitby collaborates with scholars based in United States, United Kingdom and Italy. Heidi Whitby's co-authors include Sarah T. South, Arthur R. Brothman, John C. Carey, Teresa M. Maxwell, Agatino Battaglia, Emily Aston, Xue‐Xue Zhu, Alan F. Rope, Allen N. Lamb and Cynthia J. Curry and has published in prestigious journals such as Journal of Medical Genetics, European Journal of Human Genetics and Cytogenetic and Genome Research.

In The Last Decade

Heidi Whitby

7 papers receiving 151 citations

Peers

Countries citing papers authored by Heidi Whitby

Since Specialization

Citations

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

Fields of papers citing papers by Heidi Whitby

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Heidi Whitby. 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 Heidi Whitby. The network helps show where Heidi Whitby may publish in the future.

Co-authorship network of co-authors of Heidi Whitby

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Homozygous deletions of a copy number change detected by array CGH: A new cause for mental retardation? 2008 ·American Journal of Medical Genetics Part A ·Cynthia J. Curry, Rong Mao, Emily Aston, (unknown), (unknown), Melinda Procter, (unknown), Heidi Whitby, Sarah T. South, Arthur R. Brothman	10
2	Benign copy number changes in clinical cytogenetic diagnostics by array CGH 2008 ·Cytogenetic and Genome Research ·Heidi Whitby, Anya Tsalenko, (unknown), Peter Tsang, Steven Mitchell, Pınar Bayrak‐Toydemir, Corey R. Hopkins, Greg B. Peters, Dione K. Bailey, Laurakay Bruhn, Arthur R. Brothman	8
3	Co‐occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf–Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith–Wiedemann or Russell–Silver phenotype 2008 ·American Journal of Medical Genetics Part A ·Sarah T. South, Heidi Whitby, Teresa M. Maxwell, Emily Aston, Arthur R. Brothman, John C. Carey	40
4	Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platform 2008 ·Journal of Medical Genetics ·(unknown), Heidi Whitby, Teresa M. Maxwell, (unknown), (unknown), (unknown), Xue‐Xue Zhu, (unknown), Sarah T. South, Arthur R. Brothman	21
5	Expansion in size of a terminal deletion: a paradigm shift for parental follow-up studies 2008 ·Journal of Medical Genetics ·Sarah T. South, Alan F. Rope, Allen N. Lamb, (unknown), (unknown), Heidi Whitby, Teresa M. Maxwell, Xue‐Xue Zhu, Arthur R. Brothman	29
6	Comprehensive analysis of Wolf–Hirschhorn syndrome using array CGH indicates a high prevalence of translocations 2007 ·European Journal of Human Genetics ·Sarah T. South, Heidi Whitby, Agatino Battaglia, John C. Carey, Arthur R. Brothman	57
7	Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation 2007 ·American Journal of Medical Genetics Part A ·Annika Svensson, Cynthia J. Curry, Sarah T. South, Heidi Whitby, Teresa M. Maxwell, Emily Aston, (unknown), Condie E. Carmack, (unknown), (unknown), Arthur R. Brothman	15

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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