Heather Williams

527 total citations
7 papers, 125 citations indexed

About

Heather Williams is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Heather Williams has authored 7 papers receiving a total of 125 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Heather Williams's work include Genomics and Rare Diseases (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Heather Williams is often cited by papers focused on Genomics and Rare Diseases (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Heather Williams collaborates with scholars based in United States, Germany and United Kingdom. Heather Williams's co-authors include Ilana Blum, Thomas Liehr, Anja Weise, Hans Scheffer, Kenji Fujiyoshi, Thuy L. Phung, Irmgard Verdorfer, Federico A. Monzon, Shuji Ogino and Ahmed Al‐Rikabi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, European Journal of Human Genetics and Frontiers in Genetics.

In The Last Decade

Heather Williams

7 papers receiving 112 citations

Peers

Heather Williams
Linda E. Green United States
Paola Masuzzo Belgium
Phil Gray United Kingdom
William William Indonesia
Hussein Mohsen United States
Franziska Boehm Luxembourg
Yuening Zhang China
Panagiotis Papachristou Sweden
S. Jones United States
Faisal M. Fadlelmola Sudan
Linda E. Green United States
Heather Williams
Citations per year, relative to Heather Williams Heather Williams (= 1×) peers Linda E. Green

Countries citing papers authored by Heather Williams

Since Specialization
Citations

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

Fields of papers citing papers by Heather Williams

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heather Williams

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

All Works

7 of 7 papers shown
1.
Liehr, Thomas, Monika Ziegler, Anja Weise, et al.. (2023). Small supernumerary marker chromosomes derived from human chromosome 11. Frontiers in Genetics. 14. 1293652–1293652. 1 indexed citations
2.
Liehr, Thomas, et al.. (2022). Non-Invasive Prenatal Testing in Germany. Diagnostics. 12(11). 2816–2816. 11 indexed citations
3.
Liehr, Thomas, et al.. (2021). Small supernumerary marker chromosomes derived from chromosome 14 and/or 22. Molecular Cytogenetics. 14(1). 13–13. 3 indexed citations
4.
Fujiyoshi, Kenji, Elspeth A. Bruford, Paweł Mróz, et al.. (2021). Standardizing gene product nomenclature—a call to action. Proceedings of the National Academy of Sciences. 118(3). 19 indexed citations
5.
Liehr, Thomas, Isabel M. Carreira, Zsófia Balogh, et al.. (2019). Regarding the rights and duties of Clinical Laboratory Geneticists in genetic healthcare systems; results of a survey in over 50 countries. European Journal of Human Genetics. 27(8). 1168–1174. 9 indexed citations
6.
Williams, Heather & Ilana Blum. (2018). Defining Second Generation Open Source Intelligence (OSINT) for the Defense Enterprise. RAND Corporation eBooks. 52 indexed citations
7.
Williams, Heather, et al.. (2013). Mathematical modeling of regulatory T cell effects on renal cell carcinoma treatment. Discrete and Continuous Dynamical Systems - B. 18(4). 915–943. 30 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 Linda E. Green Breakdown of academic impact, for papers by Paola Masuzzo Breakdown of academic impact, for papers by Phil Gray Breakdown of academic impact, for papers by William William Breakdown of academic impact, for papers by Hussein Mohsen Breakdown of academic impact, for papers by Franziska Boehm Breakdown of academic impact, for papers by Yuening Zhang Breakdown of academic impact, for papers by Panagiotis Papachristou Breakdown of academic impact, for papers by S. Jones Breakdown of academic impact, for papers by Faisal M. Fadlelmola
Rankless by CCL
2026