G. R. DeLong

2.5k total citations
24 papers, 1.8k citations indexed

About

G. R. DeLong is a scholar working on Cognitive Neuroscience, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, G. R. DeLong has authored 24 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cognitive Neuroscience, 12 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in G. R. DeLong's work include Genetics and Neurodevelopmental Disorders (11 papers), Autism Spectrum Disorder Research (11 papers) and Genomic variations and chromosomal abnormalities (5 papers). G. R. DeLong is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Autism Spectrum Disorder Research (11 papers) and Genomic variations and chromosomal abnormalities (5 papers). G. R. DeLong collaborates with scholars based in United States and China. G. R. DeLong's co-authors include Michael L. Cuccaro, John R. Gilbert, Ruth K. Abramson, H Wright, Richard L. Sidman, Marisa M. Menold, Daniel C. Shannon, Frank R. Brown, S. L. Donnelly and Eden R. Martin and has published in prestigious journals such as New England Journal of Medicine, The Lancet and American Journal of Clinical Nutrition.

In The Last Decade

G. R. DeLong

23 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G. R. DeLong United States	18	945	900	433	300	253	24	1.8k
Caterina Nascimbene Italy	8	1.0k 1.1×	644 0.7×	350 0.8×	142 0.5×	172 0.7×	16	2.0k
Naoko Narita Japan	24	521 0.6×	768 0.9×	1.4k 3.3×	132 0.4×	328 1.3×	50	2.6k
Izabela Kuchna United States	19	518 0.5×	541 0.6×	507 1.2×	148 0.5×	142 0.6×	37	1.5k
Krassimira Garbett United States	21	529 0.6×	471 0.5×	868 2.0×	257 0.9×	266 1.1×	35	2.6k
John M. Bissonnette United States	26	604 0.6×	867 1.0×	760 1.8×	439 1.5×	256 1.0×	82	2.4k
Linda S. Crnic United States	30	415 0.4×	726 0.8×	496 1.1×	199 0.7×	215 0.8×	60	2.2k
Joseph H. French United States	21	380 0.4×	350 0.4×	325 0.8×	286 1.0×	91 0.4×	39	1.7k
Julie Earle United States	9	365 0.4×	370 0.4×	389 0.9×	129 0.4×	383 1.5×	11	1.4k
Christian Richelme France	11	554 0.6×	215 0.2×	301 0.7×	235 0.8×	201 0.8×	30	1.5k
Hanna E. Stevens United States	26	457 0.5×	212 0.2×	400 0.9×	394 1.3×	159 0.6×	69	1.9k

Countries citing papers authored by G. R. DeLong

Since Specialization

Citations

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

Fields of papers citing papers by G. R. DeLong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. R. DeLong

This figure shows the co-authorship network connecting the top 25 collaborators of G. R. DeLong. A scholar is included among the top collaborators of G. R. DeLong 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 G. R. DeLong. G. R. DeLong 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

Ashley‐Koch, Allison E., Hao Mei, James Jaworski, et al.. (2006). An Analysis Paradigm for Investigating Multi‐locus Effects in Complex Disease: Examination of Three GABA_A Receptor Subunit Genes on 15q11‐q13 as Risk Factors for Autistic Disorder.. Annals of Human Genetics. 70(3). 281–292. 46 indexed citations

Whitehead, Patrice L., Marisa M. Menold, Eden R. Martin, et al.. (2005). Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism. The American Journal of Human Genetics. 77(3). 377–388. 269 indexed citations

Jaworski, James, Marisa M. Menold, S. L. Donnelly, et al.. (2005). Ordered‐subset analysis of savant skills in autism for 15q11‐q13. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 135B(1). 38–41. 20 indexed citations

Skaar, David, Yujun Shao, J.L. Haines, et al.. (2004). Analysis of the RELN gene as a genetic risk factor for autism. Molecular Psychiatry. 10(6). 563–571. 145 indexed citations

Shao, Yujun, Michael L. Cuccaro, Elizabeth R. Hauser, et al.. (2003). Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes. The American Journal of Human Genetics. 72(3). 539–548. 272 indexed citations

Raiford, Kimberly L., Irving C. Allen, Eden R. Martin, et al.. (2003). No association between the APOE gene and autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 125B(1). 57–60. 13 indexed citations

Bass, Meredyth P., Marisa M. Menold, Chantelle M. Wolpert, et al.. (2000). Genetic studies in autistic disorder and chromosome 15. Neurogenetics. 2(4). 219–226. 79 indexed citations

Bass, Meredyth P., Marisa M. Menold, Chantelle M. Wolpert, et al.. (2000). Genetic studies in autistic disorder and chromosome 15. Neurogenetics. 2(4). 219–219. 6 indexed citations

Martin, Eden R., Chantelle M. Wolpert, Meredyth P. Bass, et al.. (2000). Analysis of linkage disequilibrium in ?-aminobutyric acid receptor subunit genes in autistic disorder. American Journal of Medical Genetics. 96(1). 43–48. 121 indexed citations

10.

DeLong, G. R.. (1999). Neurologic Complications of Immunization. Journal watch. 1999.

11.

Ashley‐Koch, Allison E., Chantelle M. Wolpert, Marisa M. Menold, et al.. (1999). Genetic Studies of Autistic Disorder and Chromosome 7. Genomics. 61(3). 227–236. 147 indexed citations

12.

DeLong, G. R.. (1996). ‘Iodine and brain development’. Developmental Medicine & Child Neurology. 38(3). 279–280. 5 indexed citations

13.

Dou, Z. L., et al.. (1994). Iodination of irrigation water as a method of supplying iodine to a severely iodine-deficient population in XinJiang, China. The Lancet. 344(8915). 107–110. 77 indexed citations

14.

DeLong, G. R.. (1993). Effects of nutrition on brain development in humans. American Journal of Clinical Nutrition. 57(2). 286S–290S. 51 indexed citations

15.

DeLong, G. R., et al.. (1987). The 14 & 6-Associated Clinical Complex: A Rejected Hypothesis Revisited. Journal of Child Neurology. 2(2). 117–127. 6 indexed citations

16.

Todres, I. David, et al.. (1984). Neurodevelopmental outcome of survivors with posthemorrhagic hydrocephalus following grade II neonatal intraventricular hemorrhage. Annals of Neurology. 15(2). 201–204. 13 indexed citations

17.

DeLong, G. R., et al.. (1981). Acquired Reversible Autistic Syndrome in Acute Encephalopathic Illness in Children. Archives of Neurology. 38(3). 191–194. 131 indexed citations

18.

Momose, Kimito, et al.. (1977). Evaluation of Neonatal Intracranial Hemorrhage by Computerized Tomography. PEDIATRICS. 59(2). 165–172. 66 indexed citations

19.

DeLong, G. R., et al.. (1975). Sylvian aqueduct syndrome as a sign of acute obstructive hydrocephalus in children.. Journal of Neurology Neurosurgery & Psychiatry. 38(3). 288–296. 30 indexed citations

20.

DeLong, G. R. & Richard L. Sidman. (1962). Effects of eye removal at birth on histogenesis of the mouse superior colliculus: An autoradiographic analysis with tritiated thymidine. The Journal of Comparative Neurology. 118(2). 205–223. 115 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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