Clinton T. Baldwin

27.3k citations

127 papers · 6.2k indexed · h-index 42

Molecular Biology top 2%
Genetics top 0.5%
Genetics top 1%
Hematology top 0.5%
Pediatrics, Perinatology and Child Health top 1%

Co-authors: Martin H. Steinberg Lindsay A. Farrer Paola Sebastiani Darwin J. Prockop Aubrey Milunsky Christopher F. Hoth Val Nolan Nadia Solovieff
Topics: Hemoglobinopathies and Related Disorders (47 papers)Iron Metabolism and Disorders (29 papers)Folate and B Vitamins Research (12 papers)
Cited by: Genetics Hematology Aging
Journals: Nature Proceedings of the National Academy of Sciences Journal of Biological Chemistry
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 of co-authors of Clinton T. Baldwin

This figure shows the co-authorship network connecting the top 25 collaborators of Clinton T. Baldwin. A scholar is included among the top collaborators of Clinton T. Baldwin 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 Clinton T. Baldwin. Clinton T. Baldwin 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	Identification of a dominant MYH11 causal variant in chronic intestinal pseudo‐obstruction: Results of whole‐exome sequencing 2019 ·Clinical Genetics ·Weilai Dong,Clinton T. Baldwin,Jungmin Choi,Jeff M. Milunsky,Junhui Zhang,Kaya Bilgüvar,Richard P. Lifton,Aubrey Milunsky	18
2	BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia 2015 ·Blood Cells Molecules and Diseases ·Paola Sebastiani,John J. Farrell,(unknown),(unknown),(unknown),Heather M. Shappell,Harold Bae,Jacqueline N. Milton,Clinton T. Baldwin,Abdullah M. Al‐Rubaish,Zaki A. Naserullah,Fahd A Al-Muhanna,Ahmed Alsuliman,(unknown),Lindsay A. Farrer,Duyen Ngo,Vinod Vathipadiekal,David H.K. Chui,Amein K. Al‐Ali,Martin H. Steinberg	32
3	Genetic determinants of haemolysis in sickle cell anaemia 2013 ·British Journal of Haematology ·Jacqueline N. Milton,Helen Rooks,Emma Drašar,Elizabeth L. McCabe,Clinton T. Baldwin,(unknown),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)	37
4	Genome-Wide Meta-Analysis of Systolic Blood Pressure in Children with Sickle Cell Disease 2013 ·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	17
5	Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype 2013 ·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,(unknown),Zaki A. Naserullah,Idowu Akinsheye,Patrick G. Gallagher,Hongyuan Luo,David H.K. Chui,John Farrell,Amein K. Al‐Ali,Abdulrahman Alsultan	42
6	The retinoid-related orphan receptor alpha (RORA) gene and fear-related psychopathology 2013 ·Journal of Affective Disorders ·Mark W. Miller,Erika J. Wolf,Mark W. Logue,Clinton T. Baldwin	34
7	Ancestry of African Americans with sickle cell disease 2011 ·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	31
8	Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations 2007 ·American Journal of Hematology ·Paola Sebastiani,Ling Wang,Val Nolan,Efthymia Melista,Qianli Ma,Clinton T. Baldwin,Martin H. Steinberg	27
9	Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea 2007 ·The Pharmacogenomics Journal ·Qianli Ma,Diego F. Wyszynski,John J. Farrell,Abdullah Kutlar,Lindsay A. Farrer,Clinton T. Baldwin,Martin H. Steinberg	92
10	Association of Polymorphisms in the Angiotensin-Converting Enzyme Gene with Alzheimer Disease in an Israeli Arab Community 2006 ·The American Journal of Human Genetics ·Yan Meng,Clinton T. Baldwin,Abdalla Bowirrat,(unknown),Rivka Inzelberg,Robert P. Friedland,Lindsay A. Farrer	59
11	Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B 2006 ·American Journal of Hematology ·Val Nolan,Qianli Ma,Herbert T. Cohen,Adeboye H. Adewoye,Anne C. Rybicki,Clinton T. Baldwin,(unknown),Erica P. Homan,Diego F. Wyszynski,Mary E. Fabry,Ronald L. Nagel,Lindsay A. Farrer,Martin H. Steinberg	34
12	Polymorphisms in the PON gene cluster are associated with Alzheimer disease 2005 ·Human Molecular Genetics ·Porat M. Erlich,Kathryn L. Lunetta,L. Adrienne Cupples,(unknown),Robert C. Green,Clinton T. Baldwin,Lindsay A. Farrer	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 2005 ·Neuropsychiatric Disease and Treatment ·Abdalla Bowirrat,Jing Cui,(unknown),Robert P. Friedland,Marlene Oscar‐Berman,Lindsay A. Farrer,Amos D. Korczyn,Clinton T. Baldwin	3
14	Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms 2004 ·Nature ·Maya Saleh,John P. Vaillancourt,Rona K. Graham,(unknown),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	320
15	Genetic and Environmental Epidemiology of Alzheimer's Disease in Arabs Residing in Israel 2003 ·Journal of Molecular Neuroscience ·Lindsay A. Farrer,Robert P. Friedland,Abdalla Bowirrat,(unknown),Amos D. Korczyn,Clinton T. Baldwin	20
16	Genetic Loci Influencing Lung Function: A Genomewide Scan in the Framingham Study 2002 ·American Journal of Respiratory and Critical Care Medicine ·(unknown),J. B. Wilk,L. Adrienne Cupples,(unknown),Amanda M. Shearman,Clinton T. Baldwin,George O'connor,Richard H. Myers,Daniel J. Gottlieb	61
17	A locus for autosomal recessive achromatopsia on human chromosome 8q 1999 ·Clinical Genetics ·Aubrey Milunsky,(unknown),Jeff M. Milunsky,Anita L. DeStefano,Clinton T. Baldwin	16
18	Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3. 1996 ·PubMed ·Batsheva Bonné‐Tamir,Anita L. DeStefano,Christine Briggs,(unknown),(unknown),(unknown),M. Korostishevsky,Moshe Frydman,Clinton T. Baldwin,Lindsay A. Farrer	88
19	Mutations in PAX3 associated with waardenburg syndrome type I 1994 ·Human Mutation ·Clinton T. Baldwin,(unknown),Christopher F. Hoth,Tirza Cohen,Wilfred Mamuya,Aubrey Milunsky	53
20	An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome 1992 ·Nature ·Clinton T. Baldwin,Christopher F. Hoth,Jean Amos,Elias O. Da‐Silva,Aubrey Milunsky	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) and Folate and B Vitamins Research (12 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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