Babette Gwynn

3.9k citations

36 papers · 2.5k indexed · 1 hit paper · h-index 22

Physiology top 2%
Molecular Biology top 10%
Cell Biology top 2%
Genetics top 5%
Epidemiology top 10%

Co-authors: E H Birkenmeier Luanne L. Peters Carole Vogler Susan T. Howard Joseph Jerry William Landschulz Steven L. McKnight Jeffrey I. Gordon
Topics: Erythrocyte Function and Pathophysiology (14 papers)Lysosomal Storage Disorders Research (8 papers)Hemoglobinopathies and Related Disorders (6 papers)
Cited by: Physiology Cell Biology Genetics
Journals: Nature Cell Proceedings of the National Academy of Sciences
Partner nations: United States India Israel

In The Last Decade

Babette Gwynn

35 papers receiving 2.5k 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.

Tissue-specific expression, developmental regulation, and genetic mapping of the gene encoding CCAAT/enhancer binding protein.

1989 594 citations E H Birkenmeier, Babette Gwynn et al. Genes & Development profile →

Peers

Countries citing papers authored by Babette Gwynn

Since Specialization

Citations

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

Fields of papers citing papers by Babette Gwynn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Babette Gwynn

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Differential effects of RASA3 mutations on hematopoiesis are profoundly influenced by genetic background and molecular variant 2020 ·PLoS Genetics ·Raymond F. Robledo,Steven L. Ciciotte,Joel H. Graber,Yue Zhao,Amy J. Lambert,Babette Gwynn,(unknown),(unknown),(unknown),Lionel Blanc,Luanne L. Peters	3
2	Targeted deletion of βIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes 2010 ·Proceedings of the National Academy of Sciences ·Michael C. Stankewich,Babette Gwynn,Thomas Ardito,Lan Ji,Jung Kim,Raymond F. Robledo,Samuel E. Lux,Luanne L. Peters,Jon S. Morrow	59
3	A mouse TRAPP-related protein is involved in pigmentation 2006 ·Genomics ·Babette Gwynn,Richard S. Smith,Lucy B. Rowe,Benjamin A. Taylor,Luanne L. Peters	24
4	Absence of Erythroblast Macrophage Protein (Emp) Leads to Failure of Erythroblast Nuclear Extrusion 2006 ·Journal of Biological Chemistry ·Shivani Soni,Shashi Bala,Babette Gwynn,Kenneth E. Sahr,Luanne L. Peters,Manjit Hanspal	114
5	Reduced pigmentation (rp), a mouse model of Hermansky-Pudlak syndrome, encodes a novel component of the BLOC-1 complex 2004 ·Blood ·Babette Gwynn,José A. Martina,Juan S. Bonifacino,Elena V. Sviderskaya,M. Lynn Lamoreux,Dorothy C. Bennett,Kengo Moriyama,Marjan Huizing,Amanda Helip‐Wooley,William A. Gahl,(unknown),Amy J. Lambert,Luanne L. Peters	45
6	A New Spectrin, βIV, Has a Major Truncated Isoform That Associates with Promyelocytic Leukemia Protein Nuclear Bodies and the Nuclear Matrix 2001 ·Journal of Biological Chemistry ·William Tse,Ju Tang,Ou Jin,Catherine Korsgren,Kathryn M. John,Andrew L. Kung,Babette Gwynn,Luanne L. Peters,Samuel E. Lux	48
7	Downeast Anemia (dea), a New Mouse Model of Severe Nonspherocytic Hemolytic Anemia Caused by Hexokinase (HKI) Deficiency 2001 ·Blood Cells Molecules and Diseases ·Luanne L. Peters,PRISCILLA W. LANE,(unknown),Babette Gwynn,Jane E. Barker,Ernest Beutler	17
8	Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3–independent mechanism 2000 ·Blood ·Babette Gwynn,Steven L. Ciciotte,Susan J. Hunter,Linda L. Washburn,Richard S. Smith,(unknown),Richard T. Swank,Esteban C. Dell’Angelica,Juan S. Bonifacino,Eva M. Eicher,Luanne L. Peters	34
9	Mild spherocytosis and altered red cell ion transport in protein 4.2–null mice 1999 ·Journal of Clinical Investigation ·Luanne L. Peters,(unknown),Babette Gwynn,(unknown),Kathryn M. John,Samuel E. Lux,Narla Mohandas,Carl M. Cohen,Michael Cho,David E. Golan,Carlo Brugnara	65
10	Intracisternal A-Particle Element Transposition into the Murine β-Glucuronidase Gene Correlates with Loss of Enzyme Activity: a New Model for β-Glucuronidase Deficiency in the C3H Mouse 1998 ·Molecular and Cellular Biology ·Babette Gwynn,Kira K. Lueders,Mark S. Sands,E H Birkenmeier	37
11	The Gene Encoding Protein 4.2 Is Distinct from the Mouse Platelet Storage Pool Deficiency Mutation Pallid 1997 ·Genomics ·Babette Gwynn,(unknown),Carl M. Cohen,Steven L. Ciciotte,Luanne L. Peters	13
12	Murine mucopolysaccharidosis type VII: long term therapeutic effects of enzyme replacement and enzyme replacement followed by bone marrow transplantation. 1997 ·Journal of Clinical Investigation ·Mark S. Sands,Carole Vogler,(unknown),Beth Levy,Babette Gwynn,Jeffrey H. Grubb,William S. Sly,E H Birkenmeier	109
13	Genetic Localization ofCd63,a Member of the Transmembrane 4 Superfamily, Reveals Two Distinct Loci in the Mouse Genome 1996 ·Genomics ·Babette Gwynn,Eva M. Eicher,Luanne L. Peters	7
14	Anion Exchanger 1 (Band 3) Is Required to Prevent Erythrocyte Membrane Surface Loss but Not to Form the Membrane Skeleton 1996 ·Cell ·Luanne L. Peters,Ramesh A. Shivdasani,Shih‐Chun Liu,Manjit Hanspal,Kathryn M. John,Jennifer M. Reingle González,Carlo Brugnara,Babette Gwynn,Narla Mohandas,Seth L. Alper,Stuart H. Orkin,Samuel E. Lux	213
15	Reversal of pathology in murine mucopolysaccharidosis type VII by somatic cell gene transfer 1992 ·Nature ·John H. Wolfe,Mark S. Sands,Jane E. Barker,Babette Gwynn,Lucy B. Rowe,Carole Vogler,E H Birkenmeier	192
16	Tissue- and cell-specific expression of humansn-glycerol-3-phosphate dehydrogenase in transgenic mice 1992 ·Nucleic Acids Research ·E H Birkenmeier,Peter C. Hoppe,(unknown),Babette Gwynn	5
17	Increased life span and correction of metabolic defects in murine mucopolysaccharidosis type VII after syngeneic bone marrow transplantation 1991 ·Blood ·(unknown),JE Barker,(unknown),(unknown),WS Sly,Babette Gwynn,Beth Levy,(unknown)	159
18	Sequence Conservation and Structural Organization of the Glycerol-3-Phosphate Dehydrogenase Promoter in Mice and Humans 1990 ·Molecular and Cellular Biology ·Babette Gwynn,(unknown),E H Birkenmeier	4
19	Tissue-specific expression, developmental regulation, and genetic mapping of the gene encoding CCAAT/enhancer binding protein.breakdown → 1989 ·Genes & Development ·E H Birkenmeier,Babette Gwynn,Susan T. Howard,Joseph Jerry,Jeffrey I. Gordon,William Landschulz,Steven L. McKnight	594
20	Sequence of the 18S-5S ribosomal gene region and the cytochrome oxidase II gene from mtDNA of Zea diploperennis 1987 ·Theoretical and Applied Genetics ·Babette Gwynn,Ralph E. Dewey,Ronald R. Sederoff,D. H. Timothy,(unknown)	23

About Babette Gwynn

Babette Gwynn is a scholar working on Physiology, Genetics and Cell Biology, having authored 36 papers that have together received 2.5k indexed citations. Recurring topics across this work include Erythrocyte Function and Pathophysiology (14 papers), Lysosomal Storage Disorders Research (8 papers) and Hemoglobinopathies and Related Disorders (6 papers). The work is most often cited by research in Physiology (1.2k citations), Cell Biology (486 citations) and Genetics (279 citations). Babette Gwynn has collaborated with scholars based in United States, India and Israel. Frequent co-authors include E H Birkenmeier, Luanne L. Peters, Carole Vogler, Susan T. Howard, Joseph Jerry, William Landschulz, Steven L. McKnight, Jeffrey I. Gordon, Mark S. Sands and Beth Levy. Their work appears in journals such as Nature, Cell 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.

Explore authors with similar magnitude of impact