David P. Roeltgen

4.0k total citations
62 papers, 2.9k citations indexed

About

David P. Roeltgen is a scholar working on Cognitive Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, David P. Roeltgen has authored 62 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Cognitive Neuroscience, 25 papers in Genetics and 11 papers in Molecular Biology. Recurrent topics in David P. Roeltgen's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (25 papers), Neurobiology of Language and Bilingualism (14 papers) and Reading and Literacy Development (9 papers). David P. Roeltgen is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (25 papers), Neurobiology of Language and Bilingualism (14 papers) and Reading and Literacy Development (9 papers). David P. Roeltgen collaborates with scholars based in United States and Japan. David P. Roeltgen's co-authors include Judith L. Ross, Harvey Kushner, Kenneth M. Heilman, Jay S. Schneider, Andrew R. Zinn, Gerry A. Stefanatos, Gordon B. Cutler, Steven Sevush, Penelope Feuillan and Allan L. Reiss and has published in prestigious journals such as Journal of Neuroscience, Brain and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

David P. Roeltgen

61 papers receiving 2.8k citations

Peers

David P. Roeltgen
R. Holly Fitch United States
Silvia Paracchini United Kingdom
Nicole Tartaglia United States
Gerry A. Stefanatos United States
Wouter Staal Netherlands
William DeMyer United States
Jeannie Visootsak United States
R. Holly Fitch United States
David P. Roeltgen
Citations per year, relative to David P. Roeltgen David P. Roeltgen (= 1×) peers R. Holly Fitch

Countries citing papers authored by David P. Roeltgen

Since Specialization
Citations

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

Fields of papers citing papers by David P. Roeltgen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David P. Roeltgen. 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 David P. Roeltgen. The network helps show where David P. Roeltgen may publish in the future.

Co-authorship network of co-authors of David P. Roeltgen

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

All Works

20 of 20 papers shown
1.
Hong, David S., Fumiko Hoeft, Matthew Marzelli, et al.. (2014). Influence of the X-Chromosome on Neuroanatomy: Evidence from Turner and Klinefelter Syndromes. Journal of Neuroscience. 34(10). 3509–3516. 42 indexed citations
2.
Lepage, Jean‐François, David S. Hong, Mira M. Raman, et al.. (2013). Brain morphology in children with 47,XYY syndrome: a voxel‐ and surface‐based morphometric study. Genes Brain & Behavior. 13(2). 127–134. 17 indexed citations
3.
Cordeiro, Lisa, Nicole Tartaglia, David P. Roeltgen, & Judith L. Ross. (2012). Social deficits in male children and adolescents with sex chromosome aneuploidy: A comparison of XXY, XYY, and XXYY syndromes. Research in Developmental Disabilities. 33(4). 1254–1263. 77 indexed citations
4.
Hoeft, Fumiko, et al.. (2011). Neuroanatomical Phenotype of Klinefelter Syndrome in Childhood: A Voxel-Based Morphometry Study. Journal of Neuroscience. 31(18). 6654–6660. 52 indexed citations
5.
Ross, Judith L., Michèle M. M. Mazzocco, Harvey Kushner, et al.. (2009). Effects of Treatment with Oxandrolone for 4 Years on the Frequency of Severe Arithmetic Learning Disability in Girls with Turner Syndrome. The Journal of Pediatrics. 155(5). 714–720. 21 indexed citations
6.
Zinn, Andrew R., David P. Roeltgen, Gerry A. Stefanatos, et al.. (2007). A Turner syndrome neurocognitive phenotype maps to Xp22.3. Behavioral and Brain Functions. 3(1). 24–24. 52 indexed citations
7.
Ross, Judith L., David P. Roeltgen, & Andrew R. Zinn. (2006). Cognition and the Sex Chromosomes: Studies in Turner Syndrome. Hormone Research in Paediatrics. 65(1). 47–56. 71 indexed citations
8.
Ross, Judith L., Gerry A. Stefanatos, Harvey Kushner, et al.. (2004). The Effect of Genetic Differences and Ovarian Failure: Intact Cognitive Function in Adult Women with Premature Ovarian FailureVersusTurner Syndrome. The Journal of Clinical Endocrinology & Metabolism. 89(4). 1817–1822. 44 indexed citations
9.
Ross, Judith L., David P. Roeltgen, Harvey Kushner, Fanglin Wei, & Andrew R. Zinn. (2000). The Turner Syndrome–Associated Neurocognitive Phenotype Maps to Distal Xp. The American Journal of Human Genetics. 67(3). 672–681. 64 indexed citations
10.
Ross, Judith L., David P. Roeltgen, Penelope Feuillan, Harvey Kushner, & Gordon B. Cutler. (1998). Effects of Estrogen on Nonverbal Processing Speed and Motor Function in Girls with Turner’s Syndrome1. The Journal of Clinical Endocrinology & Metabolism. 83(9). 3198–3204. 102 indexed citations
11.
Ross, Judith L., Penelope Feuillan, Harvey Kushner, David P. Roeltgen, & Gordon B. Cutler. (1997). Absence of Growth Hormone Effects on Cognitive Function in Girls with Turner Syndrome1. The Journal of Clinical Endocrinology & Metabolism. 82(6). 1814–1817. 43 indexed citations
12.
Neils, Jean, et al.. (1995). Spelling and Attention in Early Alzheimer′s Disease: Evidence for Impairment of the Graphemic Buffer. Brain and Language. 49(3). 241–262. 30 indexed citations
13.
Schneider, Jay S., Zuoli Sun, & David P. Roeltgen. (1994). Effects of dihydrexidine, a full dopamine D-1 receptor agonist, on delayed response performance in chronic low dose MPTP-treated monkeys. Brain Research. 663(1). 140–144. 58 indexed citations
14.
Schneider, Jay S., Zuoli Sun, & David P. Roeltgen. (1994). Effects of dopamine agonists on delayed response performance in chronic low-dose MPTP-treated monkeys. Pharmacology Biochemistry and Behavior. 48(1). 235–240. 38 indexed citations
15.
Ross, Judith L., et al.. (1993). Neurocognitive Function and Brain Imaging in Turner Syndrome – Preliminary Results. Hormone Research. 39(2). 65–69. 14 indexed citations
16.
Roeltgen, David P.. (1992). Phonological error analysis, development and empirical evaluation*1. Brain and Language. 43(2). 190–229. 7 indexed citations
17.
Roeltgen, David P., et al.. (1991). Denial of visual perception. Brain and Cognition. 16(1). 29–40. 16 indexed citations
18.
Tucker, David M., et al.. (1988). Memory Dysfunction Following Unilateral Transection of the Fornix: A Hippocampal Disconnection Syndrome. Cortex. 24(3). 465–472. 49 indexed citations
19.
Roeltgen, David P. & David M. Tucker. (1988). Developmental phonological and lexical agraphia in adults. Brain and Language. 35(2). 287–300. 5 indexed citations
20.
Coslett, H. Branch, et al.. (1987). Transcortical sensory aphasia: Evidence for subtypes. Brain and Language. 32(2). 362–378. 31 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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