Clinton T. Baldwin

27.3k citations

127 papers · 6.2k indexed · h-index 42

Genetics top 0.5%
- Hemoglobinopathies and Related Disorders 47
- Genetic Associations and Epidemiology 11
- Connective tissue disorders research 8
Hematology top 0.5%
- Iron Metabolism and Disorders 29
- Blood groups and transfusion 10
Aging top 1%
Immunology and Allergy top 1%
- Cell Adhesion Molecules Research 10
Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics 8
Rheumatology
- Folate and B Vitamins Research 12

Co-authors: Martin H. Steinberg Lindsay A. Farrer Paola Sebastiani Darwin J. Prockop Aubrey Milunsky Christopher F. Hoth Val Nolan Nadia Solovieff
Cited by: Genetics Hematology Aging
Journals: Nature (2 papers)Proceedings of the National Academy of Sciences (1 paper)Journal of Biological Chemistry (4 papers)
Partner nations: United States Saudi Arabia Israel

In The Last Decade

Clinton T. Baldwin

124 papers receiving 6.1k citations

Peers

Countries citing papers authored by Clinton T. Baldwin

Since Specialization

Citations

This map shows the geographic impact of Clinton T. Baldwin'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 Clinton T. Baldwin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Clinton T. Baldwin more than expected).

Fields of papers citing papers by Clinton T. Baldwin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Clinton T. Baldwin. 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 Clinton T. Baldwin. The network helps show where Clinton T. Baldwin may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Identification of a dominant MYH11 causal variant in chronic intestinal pseudo‐obstruction: Results of whole‐exome sequencing Clinical Genetics ·Weilai Dong,Clinton T. Baldwin,Jungmin Choi,Jeff M. Milunsky,Junhui Zhang,Kaya Bilgüvar,Richard P. Lifton,Aubrey Milunsky	2019	18
2	BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia Blood Cells Molecules and Diseases ·Paola Sebastiani,John J. Farrell,Abdulrahman Al-Sultan,S. Wang,Heather L. Edward,Heather M. Shappell,Harold Bae,Jacqueline N. Milton,Clinton T. Baldwin,Abdullah M. Al‐Rubaish,Zaki A. Naserullah,Fahd A Al-Muhanna,Ahmed Alsuliman,P.K. Patra,Lindsay A. Farrer,Duyen Ngo,Vinod Vathipadiekal,David H.K. Chui,Amein K. Al‐Ali,Martin H. Steinberg	2015	32
3	Genetic determinants of haemolysis in sickle cell anaemia British Journal of Haematology ·Jacqueline N. Milton,Helen Rooks,Emma Drašar,Elizabeth L. McCabe,Clinton T. Baldwin,Efi Melista,Victor R. Gordeuk,Mehdi Nouraie,Gregory J. Kato,Caterina P. Minniti,James G. Taylor,Andrew Campbell,Lori Luchtman‐Jones,Sohail Rana,Oswaldo Castro,Yingze Zhang,Swee Lay Thein,Paola Sebastiani,Mark T. Gladwin,(unknown),(unknown)	2013	37
4	Genome-Wide Meta-Analysis of Systolic Blood Pressure in Children with Sickle Cell Disease PLoS ONE ·Pallav Bhatnagar,Emily Barron‐Casella,Christopher J. Bean,Jacqueline N. Milton,Clinton T. Baldwin,Martin H. Steinberg,Michael R. DeBaun,James F. Casella,Dan E. Arking	2013	17
5	Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype Blood Cells Molecules and Diseases ·Duyen Ngo,Harold Bae,Martin H. Steinberg,Paola Sebastiani,Nadia Solovieff,Clinton T. Baldwin,Efthymia Melista,Surinder Safaya,Lindsay A. Farrer,Ahmed Alsuliman,Waleed H. Albuali,Muneer H. Al Bagshi,Zaki A. Naserullah,Idowu Akinsheye,Patrick G. Gallagher,Hongyuan Luo,David H.K. Chui,John Farrell,Amein K. Al‐Ali,Abdulrahman Alsultan	2013	42
6	The retinoid-related orphan receptor alpha (RORA) gene and fear-related psychopathology Journal of Affective Disorders ·Mark W. Miller,Erika J. Wolf,Mark W. Logue,Clinton T. Baldwin	2013	34
7	Ancestry of African Americans with sickle cell disease Blood Cells Molecules and Diseases ·Nadia Solovieff,Stephen W. Hartley,Clinton T. Baldwin,Elizabeth S. Klings,Mark T. Gladwin,James G. Taylor,Gregory J. Kato,Lindsay A. Farrer,Martin H. Steinberg,Paola Sebastiani	2011	31
8	Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations American Journal of Hematology ·Paola Sebastiani,Ling Wang,Val Nolan,Efthymia Melista,Qianli Ma,Clinton T. Baldwin,Martin H. Steinberg	2007	27
9	Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea The Pharmacogenomics Journal ·Qianli Ma,Diego F. Wyszynski,John J. Farrell,Abdullah Kutlar,Lindsay A. Farrer,Clinton T. Baldwin,Martin H. Steinberg	2007	92
10	Association of Polymorphisms in the Angiotensin-Converting Enzyme Gene with Alzheimer Disease in an Israeli Arab Community The American Journal of Human Genetics ·Yan Meng,Clinton T. Baldwin,Abdalla Bowirrat,Kristin Waraska,Rivka Inzelberg,Robert P. Friedland,Lindsay A. Farrer	2006	59
11	Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B American Journal of Hematology ·Val Nolan,Qianli Ma,Herbert T. Cohen,Adeboye H. Adewoye,Anne C. Rybicki,Clinton T. Baldwin,Rhea N. Mahabir,Erica P. Homan,Diego F. Wyszynski,Mary E. Fabry,Ronald L. Nagel,Lindsay A. Farrer,Martin H. Steinberg	2006	34
12	Polymorphisms in the PON gene cluster are associated with Alzheimer disease Human Molecular Genetics ·Porat M. Erlich,Kathryn L. Lunetta,L. Adrienne Cupples,Matthew Huyck,Robert C. Green,Clinton T. Baldwin,Lindsay A. Farrer	2005	78
13	Lack of association between angiotensin-converting enzyme and dementia of the Alzheimer's type in an elderly Arab population in Wadi Ara, Israel Neuropsychiatric Disease and Treatment ·Abdalla Bowirrat,Jing Cui,Kristin Waraska,Robert P. Friedland,Marlene Oscar‐Berman,Lindsay A. Farrer,Amos D. Korczyn,Clinton T. Baldwin	2005	3
14	Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms Nature ·Maya Saleh,John P. Vaillancourt,Rona K. Graham,Matthew Huyck,Srinivasa M. Srinivasula,Emad S. Alnemri,Martin H. Steinberg,Val Nolan,Clinton T. Baldwin,Richard S. Hotchkiss,Timothy G. Buchman,Barbara A. Zehnbauer,Michael R. Hayden,Lindsay A. Farrer,Sophie Roy,Donald W. Nicholson	2004	320
15	Genetic and Environmental Epidemiology of Alzheimer's Disease in Arabs Residing in Israel Journal of Molecular Neuroscience ·Lindsay A. Farrer,Robert P. Friedland,Abdalla Bowirrat,Kristin Waraska,Amos D. Korczyn,Clinton T. Baldwin	2003	20
16	Genetic Loci Influencing Lung Function: A Genomewide Scan in the Framingham Study American Journal of Respiratory and Critical Care Medicine ·Oscar Joost,J. B. Wilk,L. Adrienne Cupples,Michael Harmon,Amanda M. Shearman,Clinton T. Baldwin,George O'connor,Richard H. Myers,Daniel J. Gottlieb	2002	61
17	A locus for autosomal recessive achromatopsia on human chromosome 8q Clinical Genetics ·Aubrey Milunsky,Xin‐Li Huang,Jeff M. Milunsky,Anita L. DeStefano,Clinton T. Baldwin	1999	16
18	Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3. PubMed ·Batsheva Bonné‐Tamir,Anita L. DeStefano,Christine Briggs,Ronald Adair,Barbara Franklyn,S Weiss,M. Korostishevsky,Moshe Frydman,Clinton T. Baldwin,Lindsay A. Farrer	1996	88
19	Mutations in PAX3 associated with waardenburg syndrome type I Human Mutation ·Clinton T. Baldwin,Nina R. Lipsky,Christopher F. Hoth,Tirza Cohen,Wilfred Mamuya,Aubrey Milunsky	1994	53
20	An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome Nature ·Clinton T. Baldwin,Christopher F. Hoth,Jean Amos,Elias O. Da‐Silva,Aubrey Milunsky	1992	385

About Clinton T. Baldwin

Clinton T. Baldwin is a scholar working on Genetics, Hematology and Aging, having authored 127 papers that have together received 6.2k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (47 papers), Iron Metabolism and Disorders (29 papers), Folate and B Vitamins Research (12 papers), Genetic Associations and Epidemiology (11 papers), Blood groups and transfusion (10 papers), Cell Adhesion Molecules Research (10 papers), Connective tissue disorders research (8 papers) and Hearing, Cochlea, Tinnitus, Genetics (8 papers). The work is most often cited by research in Genetics (1.7k citations), Hematology (1.4k citations) and Aging (195 citations). Clinton T. Baldwin has collaborated with scholars based in United States, Saudi Arabia and Israel. Frequent co-authors include Martin H. Steinberg, Lindsay A. Farrer, Paola Sebastiani, Darwin J. Prockop, Aubrey Milunsky, Christopher F. Hoth, Val Nolan, Nadia Solovieff, Leena Ala‐Kokko and David H.K. Chui. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

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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