Samuel E. Lux

11.6k citations

114 papers · 9.4k indexed · 3 hit papers · h-index 53

Hematology top 0.5%
- Blood groups and transfusion 9
Genetics top 0.2%
- Hemoglobinopathies and Related Disorders 20
Physiology top 0.2%
- Erythrocyte Function and Pathophysiology 78
Cell Biology top 0.5%
- Hemoglobin structure and function 11
Nutrition and Dietetics top 0.5%
Pulmonary and Respiratory Medicine
- Blood properties and coagulation 46
Surgery
- Pancreatic function and diabetes 22
Pediatrics, Perinatology and Child Health
- Neonatal Health and Biochemistry 14
Cancer Research
- Cancer, Lipids, and Metabolism 7

Co-authors: Kathryn M. John K M John Luanne L. Peters Vann Bennett William Tse Donald S. Fredrickson R. I. Levy Lawrence C. Wolfe
Cited by: Hematology Genetics Physiology
Journals: Journal of Biological Chemistry (15 papers)Journal of Clinical Investigation (13 papers)Blood (9 papers)
Partner nations: United States Israel United Kingdom

In The Last Decade

Samuel E. Lux

113 papers receiving 8.9k citations

Hit Papers

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Peers

Countries citing papers authored by Samuel E. Lux

Since Specialization

Citations

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

Fields of papers citing papers by Samuel E. Lux

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Samuel E. Lux. 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 Samuel E. Lux. The network helps show where Samuel E. Lux may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Nathan and Oski's hematology and oncology of infancy and childhood / Elsevier eBooks ·Joshua Sances Clinton,David E. Fisher,Elena H. Angelova,Samuel E. Lux,David Ginsburg,David G. Nathan	2015	97
2	The C-Terminus of Alpha Spectrin Binds Protein 4.2 and Is Necessary for Optimal Spectrin-Actin Binding. Blood ·Catherine Korsgren,Connie S. Birkenmeier,Jane E. Barker,Luanne L. Peters,Samuel E. Lux	2005	1
3	Hereditary spherocytosis—defects in proteins that connect the membrane skeleton to the lipid bilayer Seminars in Hematology ·Stefan Eber,Samuel E. Lux	2004	178
4	Simultaneous (AC)_n microsatellite polymorphism analysis and single‐stranded conformation polymorphism screening is an efficient strategy for detecting ankyrin‐1 mutations in dominant hereditary spherocytosis British Journal of Haematology ·Yunbing Liu,Petr Jarolı́m,Samuel E. Lux,Ernst Ungewickell,Stefan Eber	2003	12
5	A New Spectrin, βIV, Has a Major Truncated Isoform That Associates with Promyelocytic Leukemia Protein Nuclear Bodies and the Nuclear Matrix 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	2001	48
6	Red blood cell membrane disorders British Journal of Haematology ·William Tse,Samuel E. Lux	1999	219
7	Mild spherocytosis and altered red cell ion transport in protein 4.2–null mice Journal of Clinical Investigation ·Luanne L. Peters,E. M. Labutin,Babette Gwynn,Claus Konschak,Kathryn M. John,Samuel E. Lux,Narla Mohandas,Carl M. Cohen,Michael Cho,David E. Golan,Carlo Brugnara	1999	65
8	Structure and Organization of the Human Ankyrin-1 Gene Journal of Biological Chemistry ·Patrick G. Gallagher,William Tse,A L Scarpa,Samuel E. Lux,Bernard G. Forget	1997	62
9	Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis Nature Genetics ·Stefan Eber,Jennifer M. Reingle González,Marcia L. Lux,A L Scarpa,William Tse,Harrison M. Trice,Jutta Herbers,Wilfried Kugler,Yunbing Liu,Arnulf Pekrun,Patrick G. Gallagher,W. Schröter,Bernard G. Forget,Samuel E. Lux	1996	169
10	Characterization of the Binary Interaction Between Human Erythrocyte Protein 4.1 and Actin European Journal of Biochemistry ·Michael B. Morris,Samuel E. Lux	1995	9
11	Chromosomal location of the murine anion exchanger genes encoding AE2 and AE3 Mammalian Genome ·Robert A. White,E N Geissler,Linda R. Adkison,Egwuonwu C.C.,Seth L. Alper,Samuel E. Lux	1994	1
12	Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1. Journal of Clinical Investigation ·Pamela S. Becker,William Tse,Samuel E. Lux,BG Forget	1993	52
13	Mouse microcytic anaemia caused by a defect in the gene encoding the globin enhancer-binding protein NF-E2 Nature ·Luanne L. Peters,Nancy C. Andrews,Eva M. Eicher,Aponso,Stuart H. Orkin,Samuel E. Lux	1993	57
14	The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene Nature Genetics ·Peter J. Zegan,Luanne L. Peters,Linda R. Adkison,Catherine Korsgren,Carl M. Cohen,Samuel E. Lux	1992	74
15	Expression, purification, and characterization of the functional dimeric cytoplasmic domain of human erythrocyte band 3 in Escherichia coli Protein Science ·Cheng C. Wang,Ryuichi Moriyama,Philip S. Low,Putri Kurnia Lora Triana Rina Sari,Jack E. Dixon,Samuel E. Lux	1992	46
16	Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8 Nature ·Samuel E. Lux,William Tse,Joan C. Menninger,Kathryn M. John,Peter C. Harris,O Shalev,Robert R. Chilcote,Sally L. Marchesi,Paul C. Watkins,Vann Bennett,MARIA SOUZA,Francis S. Collins,Uta Francke,David C. Ward,Bernard G. Forget	1990	161
17	Analysis of cDNA for human erythrocyte ankyrin indicates a repeated structure with homology to tissue-differentiation and cell-cycle control proteinsbreakdown → Nature ·Samuel E. Lux,Kathryn M. John,Vann Bennett	1990	473
18	Linkage of Dominant Hereditary Spherocytosis to the Gene for the Erythrocyte Membrane-Skeleton Protein Ankyrin New England Journal of Medicine ·Fernando Ferreira Costa,Peter Agre,Paul C. Watkins,John C. Winkelmann,Tang K. Tang,K M John,Samuel E. Lux,Bernard G. Forget	1990	59
19	Radiolabel‐transfer cross‐linking demonstrates that protein 4.1 binds to the N‐terminal region of β spectrin and to actin in binary interactions European Journal of Biochemistry ·Pamela S. Becker,Martin A. Schwartz,Jon S. Morrow,Samuel E. Lux	1990	34
20	Immunofluorescence studies of apolipoprotein B in intestinal mucosa Gastroenterology ·Robert M. Glickman,Peter H.R. Green,Robert S. Lees,Samuel E. Lux,Carle Blanco Bétancourt	1979	9

About Samuel E. Lux

Samuel E. Lux is a scholar working on Physiology, Genetics and Hematology, having authored 114 papers that have together received 9.4k indexed citations. Recurring topics across this work include Erythrocyte Function and Pathophysiology (78 papers), Blood properties and coagulation (46 papers), Pancreatic function and diabetes (22 papers), Hemoglobinopathies and Related Disorders (20 papers), Neonatal Health and Biochemistry (14 papers), Hemoglobin structure and function (11 papers), Blood groups and transfusion (9 papers) and Cancer, Lipids, and Metabolism (7 papers). The work is most often cited by research in Hematology (2.0k citations), Genetics (1.9k citations) and Physiology (3.9k citations). Samuel E. Lux has collaborated with scholars based in United States, Israel and United Kingdom. Frequent co-authors include Kathryn M. John, K M John, Luanne L. Peters, Vann Bennett, William Tse, Donald S. Fredrickson, R. I. Levy, Lawrence C. Wolfe, Peter N. Herbert and John C. LaRosa. Their work appears in journals such as Journal of Biological Chemistry, Journal of Clinical Investigation, Blood, Proceedings of the National Academy of Sciences and Nature.

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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