Edward Moss

2.7k total citations
26 papers, 1.7k citations indexed

About

Edward Moss is a scholar working on Molecular Biology, Epidemiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Edward Moss has authored 26 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Epidemiology and 15 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Edward Moss's work include Congenital heart defects research (18 papers), Congenital Heart Disease Studies (16 papers) and Coronary Artery Anomalies (14 papers). Edward Moss is often cited by papers focused on Congenital heart defects research (18 papers), Congenital Heart Disease Studies (16 papers) and Coronary Artery Anomalies (14 papers). Edward Moss collaborates with scholars based in United States, Belgium and Poland. Edward Moss's co-authors include Elaine H. Zackai, Donna M. McDonald‐McGinn, Michael Woodin, Paul P. Wang, Marsha Gerdes, David R. Jobes, Gil Wernovsky, Robert R. Clancy, William T. Mahle and David O. Aleman and has published in prestigious journals such as NeuroImage, American Journal of Psychiatry and PEDIATRICS.

In The Last Decade

Edward Moss

26 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edward Moss United States 17 996 814 668 388 322 26 1.7k
Doron Gothelf Israel 24 1.5k 1.5× 675 0.8× 608 0.9× 801 2.1× 503 1.6× 39 2.1k
Tamar Green United States 20 632 0.6× 223 0.3× 226 0.3× 382 1.0× 286 0.9× 51 1.2k
Gilles Naeije Belgium 18 587 0.6× 189 0.2× 126 0.2× 81 0.2× 220 0.7× 73 1.6k
Daniel A. Drubach United States 25 325 0.3× 208 0.3× 91 0.1× 156 0.4× 532 1.7× 63 2.2k
Shirley Anker United Kingdom 27 180 0.2× 776 1.0× 146 0.2× 103 0.3× 732 2.3× 53 2.2k
Deborah K. Sokol United States 19 303 0.3× 59 0.1× 44 0.1× 431 1.1× 374 1.2× 56 1.1k
Sunny X. Tang United States 15 325 0.3× 163 0.2× 108 0.2× 156 0.4× 226 0.7× 48 668
Lavier Gomes Australia 21 114 0.1× 113 0.1× 93 0.1× 73 0.2× 477 1.5× 37 1.3k
Gemma Incorpora Italy 20 270 0.3× 98 0.1× 31 0.0× 376 1.0× 196 0.6× 59 1.2k
Mary R. Andriola United States 15 107 0.1× 85 0.1× 112 0.2× 137 0.4× 218 0.7× 27 1.1k

Countries citing papers authored by Edward Moss

Since Specialization
Citations

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

Fields of papers citing papers by Edward Moss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edward Moss. 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 Edward Moss. The network helps show where Edward Moss may publish in the future.

Co-authorship network of co-authors of Edward Moss

This figure shows the co-authorship network connecting the top 25 collaborators of Edward Moss. A scholar is included among the top collaborators of Edward Moss 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 Edward Moss. Edward Moss 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.
McGinn, Daniel E., T. Blaine Crowley, Tracy Heung, et al.. (2022). Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome. Genes. 13(10). 1800–1800. 2 indexed citations
2.
Gur, Ruben C., Tyler M. Moore, Ronnie Weinberger, et al.. (2021). Relationship between intelligence quotient measures and computerized neurocognitive performance in 22q11.2 deletion syndrome. Brain and Behavior. 11(8). e2221–e2221. 7 indexed citations
3.
Solot, Cynthia, Tyler M. Moore, T. Blaine Crowley, et al.. (2020). Early language measures associated with later psychosis features in 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 183(6). 392–400. 12 indexed citations
4.
Grand, Katheryn, Lorraine E. Levitt Katz, T. Blaine Crowley, et al.. (2018). The impact of hypocalcemia on full scale IQ in patients with 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 176(10). 2167–2171. 4 indexed citations
5.
McDonald‐McGinn, Donna M., Elaine H. Zackai, Harold I. Salmons, et al.. (2016). IQ and hemizygosity for the Val158Met functional polymorphism of COMT in 22q11DS. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(8). 1112–1115. 4 indexed citations
6.
Rostain, Anthony L., et al.. (2012). Transcranial Magnetic Stimulation (TMS) in the Treatment of Attention-Deficit/Hyperactivity Disorder in Adolescents and Young Adults. Journal of Ect. 28(2). 98–103. 72 indexed citations
7.
Bearden, Carrie E., Abbas F. Jawad, David R. Lynch, et al.. (2004). Effects of a Functional COMT Polymorphism on Prefrontal Cognitive Function in Patients With 22q11.2 Deletion Syndrome. American Journal of Psychiatry. 161(9). 1700–1702. 105 indexed citations
8.
Simon, Tony J., Carrie E. Bearden, Edward Moss, et al.. (2002). Cognitive development in VCFS. Progress in Pediatric Cardiology. 15(2). 109–117. 19 indexed citations
9.
Bearden, Carrie E., Michael Woodin, Edward Moss, et al.. (2001). The Neurocognitive Phenotype of the 22Q11.2 Deletion Syndrome: Selective Deficit in Visual-Spatial Memory. Journal of Clinical and Experimental Neuropsychology. 23(4). 447–464. 184 indexed citations
10.
Solot, Cynthia, Marsha Gerdes, Richard E. Kirschner, et al.. (2001). Communication issues in 22q11.2 deletion syndrome: Children at risk. Genetics in Medicine. 3(1). 67–71. 71 indexed citations
11.
Woodin, Michael, Paul P. Wang, David O. Aleman, et al.. (2001). Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion. Genetics in Medicine. 3(1). 34–39. 201 indexed citations
12.
Wang, Paul P., et al.. (2000). Research on behavioural phenotypes: velocardiofacial syndrome (deletion 22q11.2). Developmental Medicine & Child Neurology. 42(6). 422–427. 92 indexed citations
13.
Woodin, Michael, et al.. (2000). Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2). Developmental Medicine & Child Neurology. 42(6). 422–427. 25 indexed citations
14.
Solot, Cynthia, Carol Knightly, Steven D. Handler, et al.. (2000). Communication disorders in the 22Q11.2 microdeletion syndrome. Journal of Communication Disorders. 33(3). 187–204. 65 indexed citations
15.
Mahle, William T., Robert R. Clancy, Edward Moss, et al.. (2000). Neurodevelopmental Outcome and Lifestyle Assessment in School-Aged and Adolescent Children With Hypoplastic Left Heart Syndrome. PEDIATRICS. 105(5). 1082–1089. 350 indexed citations
16.
Woodin, Michael, et al.. (1999). Spatial Memory Is Impaired in Velocardiofacial/DiGeorge Syndrome,. Journal of Developmental & Behavioral Pediatrics. 20(5). 398–398. 1 indexed citations
17.
Dlugos, Dennis, Edward Moss, Ann‐Christine Duhaime, & Amy R. Brooks‐Kayal. (1999). Language-related cognitive declines after left temporal lobectomy in children. Pediatric Neurology. 21(1). 444–449. 46 indexed citations
18.
Wang, Paul P., Cynthia Solot, Edward Moss, et al.. (1998). Developmental Presentation of 22q11.2 Deletion (DiGeorge/Velocardiofacial Syndrome). Journal of Developmental & Behavioral Pediatrics. 19(5). 342–345. 17 indexed citations
19.
Davidson, Richard J., et al.. (1987). Ratings of emotion in faces are influenced by the visual field to which stimuli are presented. Brain and Cognition. 6(4). 403–411. 77 indexed citations
20.
Moss, Edward, et al.. (1952). Recurrent intussusception of the jejunum. The Journal of Pediatrics. 41(5). 587–590. 3 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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