JoAnn Bergoffen

1.9k total citations · 1 hit paper
13 papers, 1.2k citations indexed

About

JoAnn Bergoffen is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, JoAnn Bergoffen has authored 13 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cellular and Molecular Neuroscience, 4 papers in Molecular Biology and 4 papers in Pathology and Forensic Medicine. Recurrent topics in JoAnn Bergoffen's work include Hereditary Neurological Disorders (4 papers), Genetic factors in colorectal cancer (3 papers) and Colorectal Cancer Screening and Detection (3 papers). JoAnn Bergoffen is often cited by papers focused on Hereditary Neurological Disorders (4 papers), Genetic factors in colorectal cancer (3 papers) and Colorectal Cancer Screening and Detection (3 papers). JoAnn Bergoffen collaborates with scholars based in United States, United Kingdom and Poland. JoAnn Bergoffen's co-authors include K. H. Fischbeck, M. William Lensch, D Paul, Kenneth H. Fischbeck, Teresa Mattina, Marilyn C. Jones, Christopher Cunniff, Boris G. Kousseff, John M. Graham and Laura A. Penny and has published in prestigious journals such as Science, Annals of Internal Medicine and Gastroenterology.

In The Last Decade

JoAnn Bergoffen

13 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

1993 829 citations JoAnn Bergoffen, D Paul et al. Science profile →

Peers

Countries citing papers authored by JoAnn Bergoffen

Since Specialization

Citations

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

Fields of papers citing papers by JoAnn Bergoffen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of JoAnn Bergoffen

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Efficacy of paired tumor and germline testing in evaluation of patients with Lynch-like syndrome in a large integrated healthcare setting 2020 ·Familial Cancer ·(unknown), Elizabeth Hoodfar, JoAnn Bergoffen, Dan Li	4
2	Comparison of Universal Versus Age-Restricted Screening of Colorectal Tumors for Lynch Syndrome Using Mismatch Repair Immunohistochemistry 2019 ·Annals of Internal Medicine ·Dan Li, Elizabeth Hoodfar, Sheng‐Fang Jiang, Natalia Udaltsova, (unknown), (unknown), Mary Anne Armstrong, Yun‐Yi Hung, Robin J. Baker, Debbie Postlethwaite, Uri Ladabaum, Theodore R. Levin, Douglas A. Corley, JoAnn Bergoffen	16
3	Hereditary nonpolyposis colorectal cancer in young colorectal cancer patients: High-risk clinic versus population-based registry 2002 ·Gastroenterology ·Jonathan P. Terdiman, Theodore R. Levin, Brian Allen, James R. Gum, Ayelet Fishbach, Peggy Conrad, Glenn A. Miller, Vivian Weinberg, (unknown), JoAnn Bergoffen, (unknown), Neil W. Toribara, Marvin H. Sleisenger, Young S. Kim	27
4	Human Muscle Acetylcholine Receptor Alpha-subunit Gene (CHRNA1) Association with Autoimmune Myasthenia Gravis in Black, Mixed-Ancestry and Caucasian Subjects 1996 ·Journal of Autoimmunity ·Jeannine M. Heckmann, Karen Morrison, (unknown), (unknown), JoAnn Bergoffen, Nicholas Willcox, (unknown)	21
5	Consortium Fine Localization of X-Linked Charcot-Marie-Tooth Disease (CMTX1): Additional Support that Connexin32 Is the Defect in CMTX1 1995 ·Human Heredity ·Margaret A. Pericak‐Vance, (unknown), JoAnn Bergoffen, Phillip F. Chance, Susan M. Cochrane, Niklas Dahl, (unknown), Pamela R. Fain, (unknown), Kenneth H. Fischbeck, (unknown), Neva E. Haites, R. Ionasescu, Victor Ionâşescu, Marina Kennerson, Anthony P. Monaco, (unknown), Garth A. Nicholson, (unknown), Jonathan L. Haines	8
6	Clinical and molecular characterization of patients with distal 11q deletions. 1995 ·PubMed ·Laura A. Penny, Marie L. Dell’Aquila, Marilyn C. Jones, JoAnn Bergoffen, Christopher Cunniff, Jean‐Pierre Fryns, (unknown), John M. Graham, Boris G. Kousseff, Teresa Mattina	141
7	X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms. 1994 ·Journal of Medical Genetics ·Susan M. Cochrane, JoAnn Bergoffen, (unknown), E. Müller, (unknown), Anthony P. Monaco, K. H. Fischbeck, N E Haites	14
8	Familial autoimmune myasthenia gravis 1994 ·Neurology ·JoAnn Bergoffen, Chester M. Zmijewski, (unknown)	31
9	Paternal transmission of congenital myotonic dystrophy. 1994 ·Journal of Medical Genetics ·JoAnn Bergoffen, J A Kant, John T. Sladky, Donna M. McDonald‐McGinn, Elaine H. Zackai, Kenneth H. Fischbeck	23
10	Diaphragmatic hernia in tetrasomy 12p mosaicism 1993 ·The Journal of Pediatrics ·JoAnn Bergoffen, Hope H. Punnett, (unknown), Arthur J. Ross, Eduardo D. Ruchelli, Elaine H. Zackai	35
11	Linkage localization of X-linked Charcot-Marie-Tooth disease. 1993 ·PubMed ·JoAnn Bergoffen, James A. Trofatter, Jeffery M. Vance, Jonathan L. Haines, (unknown), Kenneth H. Fischbeck	67
12	Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease breakdown → 1993 ·Science ·JoAnn Bergoffen, (unknown), (unknown), (unknown), (unknown), D Paul, (unknown), M. William Lensch, (unknown), K. H. Fischbeck	829
13	Marked elevation of urinary 3‐hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long‐chainl‐3‐hydroxyacyl‐CoA dehydrogenase deficiency 1992 ·Journal of Inherited Metabolic Disease ·JoAnn Bergoffen, Paige Kaplan, Daniel E. Hale, Michael J. Bennett, Gerard T. Berry	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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