Heather Rocha

488 total citations
7 papers, 166 citations indexed

About

Heather Rocha is a scholar working on Pathology and Forensic Medicine, Genetics and Cancer Research. According to data from OpenAlex, Heather Rocha has authored 7 papers receiving a total of 166 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Pathology and Forensic Medicine, 4 papers in Genetics and 2 papers in Cancer Research. Recurrent topics in Heather Rocha's work include Genetic factors in colorectal cancer (4 papers), BRCA gene mutations in cancer (3 papers) and Genomics and Rare Diseases (2 papers). Heather Rocha is often cited by papers focused on Genetic factors in colorectal cancer (4 papers), BRCA gene mutations in cancer (3 papers) and Genomics and Rare Diseases (2 papers). Heather Rocha collaborates with scholars based in United States. Heather Rocha's co-authors include Christa Lese Martin, Alanna Kulchak Rahm, Miranda L. G. Hallquist, Adam H. Buchanan, Amy C. Sturm, Marc S. Williams, Juliann M. Savatt, H. Lester Kirchner, M. Schwartz and Tara Schmidlen and has published in prestigious journals such as Patient Education and Counseling, Genetics in Medicine and Frontiers in Genetics.

In The Last Decade

Heather Rocha

7 papers receiving 161 citations

Peers

Countries citing papers authored by Heather Rocha

Since Specialization

Citations

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

Fields of papers citing papers by Heather Rocha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heather Rocha

This figure shows the co-authorship network connecting the top 25 collaborators of Heather Rocha. A scholar is included among the top collaborators of Heather Rocha 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 Rocha. Heather Rocha 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	Low adenoma burden in unselected patients with a pathogenic APC variant 2023 ·Genetics in Medicine ·(unknown), Heather Rocha, (unknown), Juliann M. Savatt, David L. Diehl, Melissa Kelly, Marc S. Williams, Adam H. Buchanan	1
2	A RE-AIM Framework Analysis of DNA-Based Population Screening: Using Implementation Science to Translate Research Into Practice in a Healthcare System 2022 ·Frontiers in Genetics ·Laney K. Jones, Natasha T. Strande, (unknown), (unknown), (unknown), Cara Z. McCormick, Miranda L. G. Hallquist, Juliann M. Savatt, Heather Rocha, Marc S. Williams, Amy C. Sturm, Adam H. Buchanan, Russell E. Glasgow, Christa Lese Martin, Alanna Kulchak Rahm	13
3	Clinical Outcomes of a Genomic Screening Program for Actionable Genetic Conditions 2021 ·Obstetrical & Gynecological Survey ·Adam H. Buchanan, H. Lester Kirchner, M. Schwartz, Melissa Kelly, Tara Schmidlen, Laney K. Jones, Miranda L. G. Hallquist, Heather Rocha, (unknown), (unknown), (unknown), Amanda L. Lazzeri, (unknown), Alanna Kulchak Rahm, Jing Hao, Huntington F. Willard, Christa Lese Martin, David H. Ledbetter, Marc S. Williams, Amy C. Sturm	3
4	Positive impact of genetic counseling assistants on genetic counseling efficiency, patient volume, and cost in a cancer genetics clinic 2020 ·Genetics in Medicine ·Miranda L. G. Hallquist, (unknown), Michael N. Hallquist, Juliann M. Savatt, Heather Rocha, (unknown), (unknown), Yirui Hu, H. Lester Kirchner, (unknown), Alanna Kulchak Rahm, (unknown), Tara Schmidlen, M. Schwartz, Janet L. Williams, Marc S. Williams, Adam H. Buchanan	28
5	Uncertainty management for individuals with Lynch Syndrome: Identifying and responding to healthcare barriers 2020 ·Patient Education and Counseling ·Gemme Campbell‐Salome, Adam H. Buchanan, Miranda L. G. Hallquist, Alanna Kulchak Rahm, Heather Rocha, Amy C. Sturm	17
6	Clinical outcomes of a genomic screening program for actionable genetic conditions 2020 ·Genetics in Medicine ·Adam H. Buchanan, H. Lester Kirchner, M. Schwartz, Melissa Kelly, Tara Schmidlen, Laney K. Jones, Miranda L. G. Hallquist, Heather Rocha, (unknown), (unknown), (unknown), Amanda L. Lazzeri, (unknown), Alanna Kulchak Rahm, Jing Hao, Huntington F. Willard, Christa Lese Martin, David H. Ledbetter, Marc S. Williams, Amy C. Sturm	76
7	Incorporating Social Media into your Support Tool Box: Points to Consider from Genetics‐Based Communities 2017 ·Journal of Genetic Counseling ·Heather Rocha, Juliann M. Savatt, Erin Rooney Riggs, Jennifer K. Wagner, W. Andrew Faucett, Christa Lese Martin	28

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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