Gail Stetten

7.3k citations

86 papers · 5.6k indexed · 2 hit papers · h-index 29

Impact in

Genetics top 0.5%
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
Sensory Systems top 1%
- Ion Channels and Receptors

Papers in

Genetics 48
- Genomic variations and chromosomal abnormalities 30
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
Pediatrics, Perinatology and Child Health 29
- Prenatal Screening and Diagnostics 28

Co-authors: S.A. Latt Harry C. Dietz William C. Earnshaw Reed E. Pyeritz Ada Hamosh Glen M. Corson Erik G. Puffenberger Cheryl L. Maslen
Journals: Prenatal Diagnosis (9 papers)Genomics (5 papers)Fetal Diagnosis and Therapy (4 papers)Human Genetics (4 papers)Proceedings of the National Academy of Sciences (3 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

Gail Stetten

86 papers receiving 5.3k citations

Hit Papers

align trajectories log scale

TRPC1, a human homolog of a Drosophila store-operated channel. 1995 · 522 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

1995 Proceedings of the National Academy of Sciences
1991 Nature

Peers

Countries citing papers authored by Gail Stetten

Since Specialization

Citations

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

Fields of papers citing papers by Gail Stetten

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism Molecular Genetics and Metabolism ·Ying Wang, Rachel Busin, Catherine Reeves, Lena Bezman, Gerald V. Raymond, Cicely J. Toomer, Paul A. Watkins, Ann Snowden, Ann B. Moser, Sakkubai Naidu, Genila Bibat, Stacy Hewson, Karen Tam, Joe T.R. Clarke, Lawrence Charnas, Gail Stetten, Barbara Karczeski, Garry R. Cutting, Steven J. Steinberg	2011	32
2	Clinical consequences of an increasing trend of preferential use of cultured villi for molecular diagnosis by CVS Prenatal Diagnosis ·Abimbola Aina‐Mumuney, Elizabeth D. Wood, Virginia L. Corson, Gail Stetten, Shama Jari, Corinne D. Boehm, Karin J. Blakemore	2008	4
3	Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization Prenatal Diagnosis ·Colyn Cain, Daniel O. Saul, Lisa Attanasio, Erin Oehler, Ada Hamosh, Karin J. Blakemore, Gail Stetten	2007	9
4	The Principles of Clinical Cytogenetics, second edition. The American Journal of Human Genetics ·Gail Stetten	2005	6
5	In utero hematopoietic stem cell transplantation with haploidentical donor adult bone marrow in a canine model American Journal of Obstetrics and Gynecology ·Karin J. Blakemore, Catherine Hattenburg, Gail Stetten, Karin D. Berg, Sarah T. South, Kathleen M. Murphy, Richard J. Jones	2004	27
6	Reevaluating confined placental mosaicism American Journal of Medical Genetics Part A ·Gail Stetten, C. Escallon, Sarah T. South, Joseph L. McMichael, Daniel O. Saul, Karin J. Blakemore	2004	60
7	Transcript Level Alterations Reflect Gene Dosage Effects Across Multiple Tissues in a Mouse Model of Down Syndrome Genome Research ·Pascal Kahlem, Marc Sultan, Ralf Herwig, Matthias Steinfath, Daniela Balzereit, Barbara Eppens, N. Saran, Mathew T. Pletcher, Sarah T. South, Gail Stetten, Hans Lehrach, Roger H. Reeves, Marie-Laure Yaspo	2004	204
8	Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome Mammalian Genome ·Russell A. Norris, Karen K. Scott, Clara S. Moore, Gail Stetten, Cuyler R. Brown, Ethylin Wang Jabs, Eric A. Wulfsberg, Jack C. Yu, Michael J. Kern	2000	40
9	Cloning and Characterization of a Secreted Frizzled-Related Protein that is Expressed by the Retinal Pigment Epithelium Human Molecular Genetics ·Jinghua Tsai Chang, Noriko Esumi, Kathryn B. Moore, Ye Li, Shengli Zhang, C. Chew, Ben Goodman, Amir Rattner, Sally A. Moody, Gail Stetten, Peter A. Campochiaro, Donald J. Zack	1999	93
10	Genomic Structure ofPEX13,a Candidate Peroxisome Biogenesis Disorder Gene Genomics ·Jonas Björkman, Gail Stetten, Clara S. Moore, Stephen J. Gould, Denis I. Crane	1998	13
11	INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS: A COLLABORATIVE STUDY Prenatal Diagnosis ·Lillian Y. F. Hsu, Ming-Tsung Yu, K Richkind, Daniel L. Van Dyke, Barbara F. Crandall, Debra Saxe, Gabriel S. Khodr, Michael T. Mennuti, Gail Stetten, Wayne A. Miller, Jean H. Priest	1996	80
12	A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization Human Genetics ·DeniseA.S. Batista, CathyM. Tuck-Muller, JoseE. Martinez, WilliamG. Kearns, PeterL. Pearson, Gail Stetten	1993	40
13	The role of the sex-determining region of the Y chromosome (SRY) in the etiology of 46,XX true hermaphroditism Human Genetics ·Gary D. Berkovitz, Patricia Y. Fechner, Sandra M. Marcantonio, Gail Nunlee Bland, Gail Stetten, Peter N. Goodfellow, Kirby D. Smith, Claude J. Migeon	1992	83
14	Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene Nature ·Harry C. Dietz, Carry Cutting, Reed E. Pyeritz, Cheryl L. Maslen, Lynn Y. Sakai, Glen M. Corson, Erik G. Puffenberger, Ada Hamosh, Elizabeth Nanthakumar, S M Curristin, Gail Stetten, Deborah A. Meyers, Clair A. Francomano Hit paper breakdown →	1991	1466
15	Partial trisomies in two spontaneously arising long-lived human keratinocyte lines In Vitro Cellular & Developmental Biology - Animal ·Joseph D. Weaver, Gail Stetten, John W. Littlefield	1991	6
16	A Cystic Fibrosis Bronchial Epithelial Cell Line: Immortalization by Adeno-12-SV40 Infection American Journal of Respiratory Cell and Molecular Biology ·Pamela L. Zeitlin, Lili Lu, J. S. Rhim, Garry R. Cutting, Gail Stetten, K. A. Kieffer, R W Craig, William B. Guggino	1991	285
17	Origin of chromosome rearrangements in two long-lived human keratinocyte lines In Vitro Cellular & Developmental Biology - Animal ·Carla Rosenberg, Gail Stetten, W.G. Kearns, P. Pearson, John W. Littlefield	1991	4
18	Sexual discordance in monozygotic twins American Journal of Medical Genetics ·Elizabeth J. Perlman, Gail Stetten, Cathy M. Tuck‐Müller, Rosann A. Farber, W.L. Neuman, Karin J. Blakemore, Grover M. Hutchins	1990	39
19	Visualization of centromere proteins CENP-B and CENP-C on a stable dicentric chromosome in cytological spreads Chromosoma ·William C. Earnshaw, Harry Ratrie, Gail Stetten	1989	253
20	A paracentric chromosomal inversion associated with repeated early pregnancy wastage Fertility and Sterility ·Gail Stetten, John A. Rock	1983	12

About Gail Stetten

Gail Stetten is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Developmental Biology, Reproductive Medicine and Plant Science, having authored 86 papers that have together received 5.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (30 papers), Prenatal Screening and Diagnostics (28 papers), Chromosomal and Genetic Variations (21 papers), Genomics and Chromatin Dynamics (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Sexual Differentiation and Disorders (6 papers), DNA Repair Mechanisms (5 papers) and Sperm and Testicular Function (5 papers). The work is most often cited by research in Genetics (2.5k citations), Sensory Systems (397 citations), Cancer Research (582 citations), Molecular Biology (2.6k citations) and Pediatrics, Perinatology and Child Health (604 citations). Gail Stetten has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include S.A. Latt, Harry C. Dietz, William C. Earnshaw, Reed E. Pyeritz, Ada Hamosh, Glen M. Corson, Erik G. Puffenberger, Cheryl L. Maslen, Elizabeth Nanthakumar and Deborah A. Meyers. Their work appears in journals such as Prenatal Diagnosis, Genomics, Fetal Diagnosis and Therapy, Human Genetics and Proceedings of the National Academy of Sciences.

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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