Kathleen A. Leppig

8.6k citations

57 papers · 2.0k indexed · 1 hit paper · h-index 23

Cellular and Molecular Neuroscience top 5%
Neurology top 5%
Genetics top 5%
- BRCA gene mutations in cancer 16
- Genomics and Rare Diseases 13
- Genomic variations and chromosomal abnormalities 9
Neurology top 5%
Immunology and Allergy top 10%
Public Health, Environmental and Occupational Health
- Ethics in Clinical Research 8
Cancer Research
- Cancer Genomics and Diagnostics 5
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 5
Oncology
- Global Cancer Incidence and Screening 4
Pathology and Forensic Medicine
- Genetic factors in colorectal cancer 4

Co-authors: Christine M. Distèche M. William Lensch Phillip D. Swanson Shannon J. Odelberg Thomas D. Bird Brooke Smith Phillip F. Chance Norisada Matsunami
Cited by: Cellular and Molecular Neuroscience Neurology Genetics
Journals: Cell (1 paper)Proceedings of the National Academy of Sciences (2 papers)Blood (3 papers)
Partner nations: United States Canada France

In The Last Decade

Kathleen A. Leppig

55 papers receiving 1.9k citations

Hit Papers

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Peers

Countries citing papers authored by Kathleen A. Leppig

Since Specialization

Citations

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

Fields of papers citing papers by Kathleen A. Leppig

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kathleen A. Leppig. 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 Kathleen A. Leppig. The network helps show where Kathleen A. Leppig may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Kathleen A. Leppig, 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 Kathleen A. Leppig Line = papers co-authored together Kathleen A. Leppig links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	“I Didn't Have to Worry about It”: Patient and Family Experiences with Health System Involvement in Notifying Relatives of Genetic Test Results Public Health Genomics ·Paula R. Blasi,Jamilyn M. Zepp,Aaron Scrol,John Ewing,Melissa Anderson,James D. Ralston,Stephanie M. Fullerton,Kathleen A. Leppig,Nora B. Henrikson	2024	2
2	Genetic predictors of blood pressure traits are associated with preeclampsia Scientific Reports ·Elizabeth A. Jasper,Jacklyn N. Hellwege,Joseph H. Breeyear,Brenda Xiao,Gail P. Jarvik,Ian B. Stanaway,Kathleen A. Leppig,Geetha Chittoor,M. Geoffrey Hayes,Ozan Dikilitas,Iftikhar Kullo,Ingrid A. Holm,Shefali S. Verma,Todd L. Edwards,Digna R. Velez Edwards	2024	1
3	Implementation matters: How patient experiences differ when genetic counseling accompanies the return of genetic variants of uncertain significance PubMed Central ·Harsh V. Patel,Nora B. Henrikson,James D. Ralston,Kathleen A. Leppig,Aaron Scrol,Gail P. Jarvik,Shannon DeVange,Eric B. Larson,Andrea L. Hartzler	2022	0
4	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
5	Patient and Family Preferences on Health System-Led Direct Contact for Cascade Screening Journal of Personalized Medicine ·Nora B. Henrikson,Paula R. Blasi,Marlaine Figueroa Gray,Brooks Tiffany,Aaron Scrol,James D. Ralston,Stephanie M. Fullerton,Catherine Lim,John J. Ewing,Kathleen A. Leppig	2021	25
6	Effect of a Randomized Trial of a Web-Based Intervention on Patient–Provider Communication About Breast Density Journal of Women s Health ·Erin J. Aiello Bowles,Suzanne C. O’Neill,Tengfei Li,Sarah Knerr,Jeanne S. Mandelblatt,Marc D. Schwartz,Jinani Jayasekera,Kathleen A. Leppig,Kelly Ehrlich,David Farrell,Hongyuan Gao,Amanda L. Graham,George Luta,Karen J. Wernli	2021	2
7	Using Protection Motivation Theory to Predict Intentions for Breast Cancer Risk Management: Intervention Mechanisms from a Randomized Controlled Trial Journal of Cancer Education ·Claire C. Conley,Karen J. Wernli,Sarah Knerr,Tengfei Li,Kathleen A. Leppig,Kelly Ehrlich,David Farrell,Hongyuan Gao,Erin J. Aiello Bowles,Amanda L. Graham,George Luta,Jinani Jayasekera,Jeanne S. Mandelblatt,Marc D. Schwartz,Suzanne C. O’Neill	2021	2
8	Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates Genetics in Medicine ·Hana Zouk,Wanfeng Yu,Andrea M. Oza,Megan Hawley,Prathik K. Vijay Kumar,Christopher Koch,Lisa Mahanta,John B. Harley,Gail P. Jarvik,Elizabeth W. Karlson,Kathleen A. Leppig,Melanie F. Myers,Cynthia A. Prows,Marc S. Williams,Scott T. Weiss,Matthew S. Lebo,Heidi L. Rehm	2021	7
9	Participant choices for return of genomic results in the eMERGE Network Genetics in Medicine ·Christin Hoell,Julia Wynn,Luke V. Rasmussen,Keith Marsolo,Sharon Aufox,Wendy K. Chung,John J. Connolly,Robert R. Freimuth,David C. Kochan,Håkon Håkonarson,Margaret Harr,Ingrid A. Holm,Iftikhar J. Kullo,Philip E. Lammers,Kathleen A. Leppig,Nancy D. Leslie,Melanie F. Myers,Richard R. Sharp,Maureen E. Smith,Cynthia A. Prows	2020	24
10	“It would be so much easier”: health system-led genetic risk notification—feasibility and acceptability of cascade screening in an integrated system Journal of Community Genetics ·Nora B. Henrikson,Paula R. Blasi,Stephanie M. Fullerton,Jane Grafton,Kathleen A. Leppig,Gail P. Jarvik,Eric B. Larson	2019	12
11	A clinical scoring system to identify patients with sebaceous neoplasms at risk for the Muir–Torre variant of Lynch syndrome Genetics in Medicine ·Maegan E. Roberts,Douglas L. Riegert‐Johnson,Brittany C. Thomas,Kandelaria M. Rumilla,Colleen S. Thomas,Michael G. Heckman,Jennifer U. Purcell,Nancy Hanson,Kathleen A. Leppig,Justin Lim,Mark A. Cappel	2014	81
12	Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network Genetics in Medicine ·Stephanie M. Fullerton,Wendy A. Wolf,Kyle B. Brothers,Ellen Wright Clayton,Dana C. Crawford,Joshua C. Denny,Philip Greenland,Barbara A. Koenig,Kathleen A. Leppig,Noralane M. Lindor,Catherine A. McCarty,Amy L. McGuire,Eugenia McPeek Hinz,Daniel B. Mirel,Erin M. Ramos,Marylyn D. Ritchie,Maureen E. Smith,Carol Waudby,Wylie Burke,Gail P. Jarvik	2012	77
13	Fanconi anemia‐like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene American Journal of Medical Genetics Part A ·Eleanor S. Click,Barbara Cox,Susan B. Olson,Markus Grompe,Yassmine Akkari,Lisa A. Moreau,Akiko Shimamura,Darci L Sternen,Yajuan J. Liu,Kathleen A. Leppig,Dana C. Matthews,Melissa A. Parisi	2011	15
14	Motivating Factors for Physician Ordering of Factor V Leiden Genetic Tests Archives of Internal Medicine ·Lucia A. Hindorff,Wylie Burke,Anne-Marie Laberge,Kenneth Rice,Thomas Lumley,Kathleen A. Leppig,Frits R. Rosendaal,Eric B. Larson,Bruce M. Psaty	2009	16
15	Genotype–phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations Genetics in Medicine ·Jill A. Rosenfeld,Kathleen A. Leppig,Blake C. Ballif,Heidi Thiese,Christine Erdie-Lalena,Erwati Bawle,Sujatha Sastry,J. Edward Spence,Anne M. Bandholz,Urvashi Surti,Jonathan Zonana,Kory Keller,Wendy S. Meschino,Bassem A. Bejjani,Beth S. Torchia,Lisa G. Shaffer	2009	55
16	Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins The Journal of Pediatrics ·Gregory M. Enns,Robert D. Steiner,Neil R.M. Buist,Charles A. Cowan,Kathleen A. Leppig,Marjorie F. McCracken,Vibeke Westphal,Hudson H. Freeze,John F. O’Brien,Jaak Jaeken,Gert Matthijs,Sarina K. Behera,Louanne Hudgins	2002	31
17	Familial cryptic (20;21) translocation identified by in situ hybridization technologies American Journal of Medical Genetics ·Kathleen A. Leppig,Susie Ball,Kam Au,Kent E. Opheim,Thomas H. Norwood	2000	5
18	Familial neurofibromatosis 1 microdeletions: Cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromata American Journal of Medical Genetics ·Kathleen A. Leppig,Paige Kaplan,David Viskochil,Molly Weaver,June Ortenberg,Karen Stephens	1997	84
19	Smooth muscle tumors associated with X-linked Alport syndrome: Carrier detection in females Kidney International ·Karin Dahan,Laurence Heidet,Jing Zhou,Gabrielle Mettler,Kathleen A. Leppig,Willem Proesmans,Albert David,Bernard Roussel,J. G. Mongeau,James Gould,Jean‐Pierre Grünfeld,Marie-Claire Gübler,Corinne Antignac	1995	29
20	Predictive value of minor anomalies: II. Use in cohort studies to identify teratogens Teratology ·Lewis B. Holmes,B. Kleiner,Kathleen A. Leppig,Cristina I. Cann,Alvaro Muñoz,B. Frank Polk	1987	42

About Kathleen A. Leppig

Kathleen A. Leppig is a scholar working on Genetics, Cancer Research and Genetics, having authored 57 papers that have together received 2.0k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (16 papers), Genomics and Rare Diseases (13 papers), Genomic variations and chromosomal abnormalities (9 papers), Ethics in Clinical Research (8 papers), Cancer Genomics and Diagnostics (5 papers), Prenatal Screening and Diagnostics (5 papers), Global Cancer Incidence and Screening (4 papers) and Genetic factors in colorectal cancer (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (507 citations), Neurology (219 citations) and Genetics (681 citations). Kathleen A. Leppig has collaborated with scholars based in United States, Canada and France. Frequent co-authors include Christine M. Distèche, M. William Lensch, Phillip D. Swanson, Shannon J. Odelberg, Thomas D. Bird, Brooke Smith, Phillip F. Chance, Norisada Matsunami, Cristina I. Cann and Lewis B. Holmes. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and Blood.

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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