James G. Coldwell

1.4k total citations
17 papers, 620 citations indexed

About

James G. Coldwell is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, James G. Coldwell has authored 17 papers receiving a total of 620 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in James G. Coldwell's work include Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (5 papers) and Metabolism and Genetic Disorders (4 papers). James G. Coldwell is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (5 papers) and Metabolism and Genetic Disorders (4 papers). James G. Coldwell collaborates with scholars based in United States and Denmark. James G. Coldwell's co-authors include Burhan Say, Jürgen Herrmann, John M. Opitz, Giovanni Neri, John C. Carey, Paul V. Miles, James F. Reynolds, Bruce Blumberg, Richard Koch and Bobbye Rouse and has published in prestigious journals such as American Journal of Psychiatry, The Journal of Pediatrics and Clinica Chimica Acta.

In The Last Decade

James G. Coldwell

17 papers receiving 582 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
James G. Coldwell United States	13	357	222	177	125	84	17	620
Maja Di Rocco Italy	12	212 0.6×	122 0.5×	69 0.4×	131 1.0×	56 0.7×	20	459
C. Aulehla‐Scholz Germany	14	344 1.0×	312 1.4×	96 0.5×	46 0.4×	55 0.7×	27	703
Alan S. Lidsky United States	9	582 1.6×	577 2.6×	142 0.8×	106 0.8×	39 0.5×	10	855
Robert L. Conway United States	13	338 0.9×	100 0.5×	298 1.7×	147 1.2×	119 1.4×	23	723
Andrew Orr Canada	12	348 1.0×	65 0.3×	226 1.3×	48 0.4×	58 0.7×	17	735
Natalie Hauser United States	13	293 0.8×	111 0.5×	228 1.3×	32 0.3×	58 0.7×	26	562
Khalid Al‐Thihli Oman	13	219 0.6×	135 0.6×	116 0.7×	66 0.5×	58 0.7×	50	456
Catherine Brunel‐Guitton Canada	14	454 1.3×	203 0.9×	38 0.2×	66 0.5×	41 0.5×	28	621
R. M. Brown United Kingdom	18	663 1.9×	561 2.5×	164 0.9×	102 0.8×	30 0.4×	27	1.0k
Jutta Gärtner Germany	14	366 1.0×	56 0.3×	109 0.6×	60 0.5×	22 0.3×	19	650

Countries citing papers authored by James G. Coldwell

Since Specialization

Citations

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

Fields of papers citing papers by James G. Coldwell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James G. Coldwell. 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 James G. Coldwell. The network helps show where James G. Coldwell may publish in the future.

Co-authorship network of co-authors of James G. Coldwell

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

All Works

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17 of 17 papers shown

Nagamani, Sandesh C. Sreenath, Ayelet Erez, Christine M. Eng, et al.. (2008). Interstitial deletion of 6q25.2–q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss. European Journal of Human Genetics. 17(5). 573–581. 39 indexed citations

Koch, Richard, Barbara K. Burton, George Hoganson, et al.. (2002). Phenylketonuria in adulthood: A collaborative study. Journal of Inherited Metabolic Disease. 25(5). 333–346. 162 indexed citations

Fu, Jun, et al.. (2001). Quantitative amino acid analysis using a Beckman system gold HPLC 126AA analyzer. Clinica Chimica Acta. 312(1-2). 153–162. 42 indexed citations

Surendran, Sankar, et al.. (2001). Malonyl CoA decarboxylase deficiency: C to T transition in intron 2 of the MCD gene. Journal of Neuroscience Research. 65(6). 591–594. 14 indexed citations

Velagaleti, Gopalrao V.N., Stephen E. Harris, Nancy J. Carpenter, James G. Coldwell, & Burhan Say. (1996). Familial deletion of chromosome 18 (p11.2).. PubMed. 39(4). 201–4. 18 indexed citations

Rao, V.V.N. Gopal, et al.. (1995). Partial trisomy 13q identified by sequential fluorescence in situ hybridization. American Journal of Medical Genetics. 58(1). 50–53. 11 indexed citations

Wilson, Don P., et al.. (1989). Nephropathic cystinosis: Improved linear growth after treatment with recombinant human growth hormone. The Journal of Pediatrics. 115(5). 758–761. 18 indexed citations

Reynolds, James F., Giovanni Neri, Jürgen Herrmann, et al.. (1986). New multiple congenital anomalies/mental retardation syndrome with cardio‐facio‐cutaneous involvement—the CFC syndrome. American Journal of Medical Genetics. 25(3). 413–427. 159 indexed citations

Say, Burhan, Nancy J. Carpenter, & James G. Coldwell. (1979). Familial Gynecomastia Without Hypogonadism. Southern Medical Journal. 72(10). 1330–1331. 1 indexed citations

10.

Say, Burhan, et al.. (1977). THE RADIAL DYSPLASIA/IMPERFORATE ANUS/VERTEBRAL ANOMALIES SYNDROME (THE VATER ASSOCIATION): DEVELOPMENTAL ASPECTS AND EYE FINDINGS. Acta Paediatrica. 66(2). 233–235. 12 indexed citations

11.

Carpenter, Nancy J., et al.. (1977). Chromosome variants in children with psychiatric disorders. American Journal of Psychiatry. 134(4). 424–426. 10 indexed citations

12.

Say, Burhan, et al.. (1976). Familial translocation (3p 15p) with partial trisomy for the upper arm of chromosome 3 in two sibs. The Journal of Pediatrics. 88(3). 447–450. 22 indexed citations

13.

Say, Burhan, et al.. (1976). Polydactyly with triphalangeal thumbs, brachydactyly, camptodactyly, congenital dislocation of the patellas, short stature and borderline intelligence.. PubMed. 12(5). 279–86. 8 indexed citations

14.

Say, Burhan, et al.. (1975). A new dominantly inherited syndrome of cleft palate. PubMed. 26(3). 267–269. 12 indexed citations

15.

Say, Burhan & James G. Coldwell. (1975). Hereditary defect of the sacrum. Human Genetics. 27(3). 231–234. 22 indexed citations

16.

Francke, Uta, Bohdan Bakay, James D. Connor, James G. Coldwell, & William L. Nyhan. (1974). Linkage relationships of X-linked enzymes glucose-6-phosphate dehydrogenase and hypoxanthine guanine phosphoribosyltransferase: recombination in female offspring of compound heterozygotes.. PubMed. 26(4). 512–22. 14 indexed citations

17.

Frankenburg, William K., et al.. (1968). Maternal phenylketonuria: Implications for growth and development. The Journal of Pediatrics. 73(4). 560–570. 56 indexed citations

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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