Georgia L. Wiesner

13.1k citations

76 papers · 3.0k indexed · 1 hit paper · h-index 28

Genetics top 1%
- BRCA gene mutations in cancer 31
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 7
Pathology and Forensic Medicine top 2%
- Genetic factors in colorectal cancer 19
Cancer Research top 5%
- Cancer Genomics and Diagnostics 11
Oncology top 5%
- Colorectal Cancer Screening and Detection 7
Molecular Biology top 10%
Public Health, Environmental and Occupational Health
- Ethics in Clinical Research 12
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 5

Co-authors: Heather Hampel Robin L. Bennett Adam H. Buchanan Rachel Pearlman Louise S. Acheson Thomas A. Sellers Joseph Willis Sanford D. Markowitz
Cited by: Genetics Pathology and Forensic Medicine Cancer Research
Journals: New England Journal of Medicine (1 paper)Proceedings of the National Academy of Sciences (1 paper)JAMA (1 paper)
Partner nations: United States New Zealand France

In The Last Decade

Georgia L. Wiesner

74 papers receiving 2.9k citations

Hit Papers

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Peers

Countries citing papers authored by Georgia L. Wiesner

Since Specialization

Citations

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

Fields of papers citing papers by Georgia L. Wiesner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Georgia L. Wiesner. 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 Georgia L. Wiesner. The network helps show where Georgia L. Wiesner may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Georgia L. Wiesner, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Georgia L. Wiesner Line = papers co-authored together Georgia L. Wiesner links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Oopherectomy in a Child to Reduce Cancer Risk: Oncogenetic, Ethical, and Legal Considerations PEDIATRICS ·Jennifer Brewer,Georgia L. Wiesner,Ellen Wright Clayton,Daniel J. Benedetti	2025	1
2	Conducting inclusive research in genetics for transgender, gender‐diverse, and sex‐diverse individuals: Case analyses and recommendations from a clinical genomics study Journal of Genetic Counseling ·Harris T. Bland,Marian J. Gilmore,Justin Andujar,Makenna A. Martin,Natasha Celaya‐Cobbs,Clasherrol Edwards,Meredith Gerhart,Gillian W. Hooker,Stephanie A. Kraft,Dana Marshall,Lori A. Orlando,Natalie Paul,Siddharth Pratap,S. Trent Rosenbloom,Georgia L. Wiesner,Kathleen F. Mittendorf	2023	5
3	Impact of returning unsolicited genomic results to nongenetic health care providers in the eMERGE III Network Genetics in Medicine ·Jill A. Madden,Kyle K. Brothers,Janet L. Williams,Melanie F. Myers,Kathleen A. Leppig,Ellen Wright Clayton,Georgia L. Wiesner,Ingrid A. Holm	2022	3
4	Increased ease of access to genetic counseling for low-income women with breast cancer using a point of care screening tool Journal of Community Genetics ·Smita K. Rao,Kimberly Thomas,Rajbir Singh,Eden Biltibo,Philip E. Lammers,Georgia L. Wiesner	2021	2
5	Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network Frontiers in Genetics ·Marc S. Williams,Casey Overby Taylor,Nephi Walton,Scott Goehringer,Samuel Aronson,Robert R. Freimuth,Luke V. Rasmussen,Eric S. Hall,Cynthia A. Prows,Wendy K. Chung,Alexander Fedotov,Jordan G. Nestor,Chunhua Weng,Robb Rowley,Georgia L. Wiesner,Gail P. Jarvik,Guilherme Del Fiol	2019	33
6	The impact of variant classification on the clinical management of hereditary cancer syndromes Genetics in Medicine ·Scott A. Turner,Smita K. Rao,Rebecca Morgan,Cindy L. Vnencak‐Jones,Georgia L. Wiesner	2018	45
7	Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews Hereditary Cancer in Clinical Practice ·Jennifer L. Schneider,Katrina A.B. Goddard,Kristin R. Muessig,James V. Davis,Alan F. Rope,Jessica Ezzell Hunter,Susan K. Peterson,Louise S. Acheson,Sapna Syngal,Georgia L. Wiesner,Jacob A. Reiss	2018	24
8	Ethical, Legal, and Social Implications of Personalized Genomic Medicine Research: Current Literature and Suggestions for the Future Bioethics ·Shawneequa Callier,Rachel Abudu,Maxwell J. Mehlman,Mendel E. Singer,Duncan Neuhauser,Charlisse Caga‐Anan,Georgia L. Wiesner	2016	27
9	Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitators Genetics in Medicine ·Jennifer L. Schneider,James V. Davis,Tia L. Kauffman,Jacob A. Reiss,Cheryl McGinley,Kathleen Arnold,Jamilyn M. Zepp,Marian Gilmore,Kristin R. Muessig,Sapna Syngal,Louise S. Acheson,Georgia L. Wiesner,Susan K. Peterson,Katrina A.B. Goddard	2015	34
10	Inactivating Mutation in the Prostaglandin Transporter Gene, SLCO2A1 , Associated with Familial Digital Clubbing, Colon Neoplasia, and NSAID Resistance Cancer Prevention Research ·Kishore Guda,Stephen P. Fink,Ginger L. Milne,Neil Molyneaux,Lakshmeswari Ravi,S. M. Lewis,Andrew J. Dannenberg,Courtney G. Montgomery,Shulin Zhang,Joseph Willis,Georgia L. Wiesner,Sanford D. Markowitz	2014	27
11	IRB perspectives on the return of individual results from genomic research Genetics in Medicine ·Lynn G. Dressler,Sondra J. Smolek,Roselle Ponsaran,Janell M. Markey,Helene Starks,Nancy Gerson,Susan Lewis,Nancy Press,Eric T. Juengst,Georgia L. Wiesner	2012	53
12	Attitudes toward Genetic Research Review: Results from a Survey of Human Genetics Researchers Public Health Genomics ·Karen L. Edwards,Amy A. Lemke,Susan Brown Trinidad,S. M. Lewis,Helene Starks,Marianne Griffin,Georgia L. Wiesner	2011	31
13	Patient interest in recording family histories of cancer via the Internet Genetics in Medicine ·Christian Simon,Louise S. Acheson,Christopher J. Burant,Nancy Gerson,Sarah Schramm,Susan Lewis,Georgia L. Wiesner	2008	15
14	Report of Banbury Summit meeting on training of physicians in medical genetics, October 20–22, 2004 Genetics in Medicine ·Bruce R. Korf,Gerald L. Feldman,Georgia L. Wiesner	2005	27
15	Cancer genetics in primary care Primary Care Clinics in Office Practice ·Duane Culler,Sarah J. Grimes,Louise S. Acheson,Georgia L. Wiesner	2004	7
16	Methylation of the CDH1 promoter as the second genetic hit in hereditary diffuse gastric cancer Nature Genetics ·William M. Grady,Joseph Willis,Parry Guilford,Anita K. Dunbier,Tumi Toro,Henry T. Lynch,Georgia L. Wiesner,Kelly Ferguson,Charis Eng,Jae Gahb Park,Seong-Jin Kim,Sanford D. Markowitz	2000	350
17	E-cadherin mutation-based genetic counseling and hereditary diffuse gastric carcinoma Cancer Genetics and Cytogenetics ·Henry T. Lynch,William M. Grady,Jane F. Lynch,Karen D. Tsuchiya,Georgia L. Wiesner,Sanford D. Markowitz	2000	17
18	Cardiac Disease in Costello Syndrome PEDIATRICS ·Ernest Siwik,Kenneth Zahka,Georgia L. Wiesner,Chanin Limwongse	1998	30
19	Current Concepts Review Hemihypertrophy Journal of Bone and Joint Surgery ·R. Tracy Ballock,Georgia L. Wiesner,Melissa T. Myers,George H. Thompson	1997	38
20	Association between family history of cancer and breast cancer defined by estrogen and progesterone receptor status Genetic Epidemiology ·Angela M. Tutera,Thomas A. Sellers,John D. Potter,Carol R. Drinkard,Georgia L. Wiesner,Aaron R. Folsom	1996	23

About Georgia L. Wiesner

Georgia L. Wiesner is a scholar working on Genetics, Pathology and Forensic Medicine and Cancer Research, having authored 76 papers that have together received 3.0k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (31 papers), Genetic factors in colorectal cancer (19 papers), Genomics and Rare Diseases (14 papers), Ethics in Clinical Research (12 papers), Cancer Genomics and Diagnostics (11 papers), Colorectal Cancer Screening and Detection (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Prenatal Screening and Diagnostics (5 papers). The work is most often cited by research in Genetics (1.5k citations), Pathology and Forensic Medicine (760 citations) and Cancer Research (431 citations). Georgia L. Wiesner has collaborated with scholars based in United States, New Zealand and France. Frequent co-authors include Heather Hampel, Robin L. Bennett, Adam H. Buchanan, Rachel Pearlman, Louise S. Acheson, Thomas A. Sellers, Joseph Willis, Sanford D. Markowitz, Rodney A. King and William S. Oetting. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and JAMA.

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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