Steven L. Ciciotte

421 total citations
22 papers, 336 citations indexed

About

Steven L. Ciciotte is a scholar working on Physiology, Molecular Biology and Genetics. According to data from OpenAlex, Steven L. Ciciotte has authored 22 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Physiology, 9 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Steven L. Ciciotte's work include Erythrocyte Function and Pathophysiology (11 papers), Hemoglobinopathies and Related Disorders (7 papers) and Blood properties and coagulation (5 papers). Steven L. Ciciotte is often cited by papers focused on Erythrocyte Function and Pathophysiology (11 papers), Hemoglobinopathies and Related Disorders (7 papers) and Blood properties and coagulation (5 papers). Steven L. Ciciotte collaborates with scholars based in United States, Australia and Hungary. Steven L. Ciciotte's co-authors include Luanne L. Peters, Babette Gwynn, Juan S. Bonifacino, Kenneth E. Sahr, William A. Gahl, Diana M. Gilligan, Marjan Huizing, Kengo Moriyama, Raymond F. Robledo and Narla Mohandas and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and PLoS ONE.

In The Last Decade

Steven L. Ciciotte

21 papers receiving 327 citations

Peers

Countries citing papers authored by Steven L. Ciciotte

Since Specialization

Citations

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

Fields of papers citing papers by Steven L. Ciciotte

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven L. Ciciotte

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

All Works

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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	Rasa3 regulates stage-specific cell cycle progression in murine erythropoiesis 2020 ·Blood Cells Molecules and Diseases ·(unknown), Julien Papoin, (unknown), Raymond F. Robledo, Steven L. Ciciotte, Theodosia A. Kalfa, Luanne L. Peters, Lionel Blanc	3
3	A mutation in mouse Krüppel-like factor 15 alters the gut microbiome and response to obesogenic diet 2019 ·PLoS ONE ·Karen L. Svenson, (unknown), Steven L. Ciciotte, Mark D. Adams	2
4	RASA3 Is Essential for Early Mammalian Hematopoiesis and Modulates ERK Signaling in Terminal Erythropoiesis 2019 ·Blood ·(unknown), Raymond F. Robledo, Steven L. Ciciotte, Joel H. Graber, Yue Zhao, (unknown), Julien Papoin, Lionel Blanc, Luanne L. Peters	0
5	Increased Reactive Oxygen Species and Cell Cycle Defects Contribute to Anemia in the RASA3 Mutant Mouse Model scat 2018 ·Frontiers in Physiology ·(unknown), (unknown), Julien Papoin, Steven L. Ciciotte, Yue Zhao, Luanne L. Peters, Lionel Blanc	10
6	Mutant KLF1 in Adult Anemic Nan Mice Leads to Profound Transcriptome Changes and Disordered Erythropoiesis 2018 ·Scientific Reports ·Danitza Nébor, Joel H. Graber, Steven L. Ciciotte, Raymond F. Robledo, Julien Papoin, (unknown), Kevin R. Gillinder, Andrew C. Perkins, James J. Bieker, Lionel Blanc, Luanne L. Peters	15
7	3-Dimensional histological reconstruction and imaging of the murine pancreas 2014 ·Mammalian Genome ·Steven L. Ciciotte, Mark D. Lessard, Ellen C. Akeson, Elizabeth Cameron, Timothy M. Stearns, James M. Denegre, Jesús Ruberte, Karen L. Svenson	3
8	Targeted deletion of the γ‐adducin gene (Add3) in mice reveals differences in α‐adducin interactions in erythroid and nonerythroid cells 2009 ·American Journal of Hematology ·Kenneth E. Sahr, Amy J. Lambert, Steven L. Ciciotte, Narla Mohandas, Luanne L. Peters	13
9	Targeted deletion of α-adducin results in absent β- and γ-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice 2008 ·Blood ·Raymond F. Robledo, Steven L. Ciciotte, Babette Gwynn, Kenneth E. Sahr, Diana M. Gilligan, Narla Mohandas, Luanne L. Peters	52
10	Targeted Deletion of γ-Adducin in Mice. 2007 ·Blood ·Kenneth E. Sahr, Amy J. Lambert, Steven L. Ciciotte, Luanne L. Peters	2
11	Targeted Deletion of α-Adducin Results in Absent β-Adducin, Compensated Hemolytic Anemia, and Hydrocephalus in Mice. 2007 ·Blood ·Raymond F. Robledo, Steven L. Ciciotte, Babette Gwynn, Kenneth E. Sahr, Diana M. Gilligan, Luanne L. Peters	1
12	Transgenic Cre expression mice for generation of erythroid‐specific gene alterations 2004 ·genesis ·Kenneth R. Peterson, Halyna Fedosyuk, Lesya Zelenchuk, B Nakamoto, Evangelia Yannaki, George Stamatoyannopoulos, Steven L. Ciciotte, Luanne L. Peters, Linda M. Scott, Thalia Papayannopoulou	18
13	Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1) 2003 ·Blood ·Steven L. Ciciotte, Babette Gwynn, Kengo Moriyama, Marjan Huizing, William A. Gahl, Juan S. Bonifacino, Luanne L. Peters	76
14	The mouse adducin gene family: alternative splicing and chromosomal localization 2000 ·Mammalian Genome ·(unknown), (unknown), Steven L. Ciciotte, Luanne L. Peters, Diana M. Gilligan	18
15	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
16	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	3
17	cDNA sequence and chromosomal localization of mouse Dlgh3 gene adjacent to the BRCA1 tumor suppressor locus 1998 ·Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·(unknown), Luanne L. Peters, Steven L. Ciciotte, Athar H. Chishti	12
18	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
19	Limatin (LIMAB1), an Actin-Binding LIM Protein, Maps to Mouse Chromosome 19 and Human Chromosome 10q25, a Region Frequently Deleted in Human Cancers 1997 ·Genomics ·Anthony C. Kim, Luanne L. Peters, Joan H.M. Knoll, Christophe Van Huffel, Steven L. Ciciotte, Patrick W. Kleyn, (unknown)	29
20	The mouse homolog of the Drosophila discs large tumor suppressor gene maps to Chromosome 16 1996 ·Mammalian Genome ·Luanne L. Peters, Steven L. Ciciotte, Li Lin, Athar H. Chishti	1

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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