Daniel Moreno‐De‐Luca

8.1k total citations
11 papers, 332 citations indexed

About

Daniel Moreno‐De‐Luca is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Daniel Moreno‐De‐Luca has authored 11 papers receiving a total of 332 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Cognitive Neuroscience. Recurrent topics in Daniel Moreno‐De‐Luca's work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (6 papers) and Autism Spectrum Disorder Research (5 papers). Daniel Moreno‐De‐Luca is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (6 papers) and Autism Spectrum Disorder Research (5 papers). Daniel Moreno‐De‐Luca collaborates with scholars based in United States, Germany and Italy. Daniel Moreno‐De‐Luca's co-authors include Alastair J. Martin, Stephan Sanders, Jennifer K. Lowe, A. Jeremy Willsey, Daniel H. Geschwind, Matthew W. State, Jennifer G. Mullé, Andrés Moreno-De-Luca, Omar Abdul‐Rahman and Holly H. Zimmerman and has published in prestigious journals such as Molecular Psychiatry, JAMA Psychiatry and Frontiers in Psychiatry.

In The Last Decade

Daniel Moreno‐De‐Luca

9 papers receiving 325 citations

Peers

Daniel Moreno‐De‐Luca
Lauren Bush United States
Barbara Haas‐Givler United States
Joana Almeida Portugal
Jessica Zweifach United States
Latha Soorya United States
LeeAnne Green Snyder United States
Teresa Lim United States
Gabriele Schmötzer Germany
Arianne S. Wallace United States
Ingrid Tremel Barbato Brazil
Lauren Bush United States
Daniel Moreno‐De‐Luca
Citations per year, relative to Daniel Moreno‐De‐Luca Daniel Moreno‐De‐Luca (= 1×) peers Lauren Bush

Countries citing papers authored by Daniel Moreno‐De‐Luca

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Moreno‐De‐Luca

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel Moreno‐De‐Luca. 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 Daniel Moreno‐De‐Luca. The network helps show where Daniel Moreno‐De‐Luca may publish in the future.

Co-authorship network of co-authors of Daniel Moreno‐De‐Luca

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

All Works

11 of 11 papers shown
1.
Ledbetter, David H., Brenda Finucane, Daniel Moreno‐De‐Luca, & Scott M. Myers. (2025). Mainstreaming Diagnostic Genetic Testing and Precision Medicine for Autism Spectrum Disorder. Psychiatric Clinics of North America. 48(2). 343–360.
2.
Kyzar, Evan J., Melissa R. Arbuckle, Adam Abba‐Aji, et al.. (2024). Leveraging neuroscience education to address stigma related to opioid use disorder in the community: a pilot study. Frontiers in Psychiatry. 15. 1360356–1360356.
3.
Moreno‐De‐Luca, Daniel, Andrés Moreno-De-Luca, Joseph F. Cubells, & Stephan Sanders. (2014). Cross-Disorder Comparison of Four Neuropsychiatric CNV Loci. 2(3). 151–161. 17 indexed citations
4.
Moreno-De-Luca, Andrés, David W. Evans, K. B. Boomer, et al.. (2014). The Role of Parental Cognitive, Behavioral, and Motor Profiles in Clinical Variability in Individuals With Chromosome 16p11.2 Deletions. JAMA Psychiatry. 72(2). 119–119. 94 indexed citations
5.
Moreno‐De‐Luca, Daniel, Stephan Sanders, A. Jeremy Willsey, et al.. (2012). Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts. Molecular Psychiatry. 18(10). 1090–1095. 111 indexed citations
6.
Moreno‐De‐Luca, Daniel & Joseph F. Cubells. (2011). Copy Number Variants: A New Molecular Frontier in Clinical Psychiatry. Current Psychiatry Reports. 13(2). 129–137. 6 indexed citations
7.
Delorme, Richard, Daniel Moreno‐De‐Luca, Wolfgang Maier, et al.. (2010). Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder. BMC Medical Genetics. 11(1). 100–100. 12 indexed citations
8.
Devillard, Françoise, Vincent Guinchat, Daniel Moreno‐De‐Luca, et al.. (2010). Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism. American Journal of Medical Genetics Part A. 152A(9). 2346–2354. 14 indexed citations
9.
Carr, Christopher W., Daniel Moreno‐De‐Luca, Colette C. Parker, et al.. (2010). Chiari I malformation, delayed gross motor skills, severe speech delay, and epileptiform discharges in a child with FOXP1 haploinsufficiency. European Journal of Human Genetics. 18(11). 1216–1220. 60 indexed citations
10.
Giegling, Ina, Daniel Moreno‐De‐Luca, Raffaella Calati, et al.. (2009). Tyrosine Hydroxylase and DOPA Decarboxylase Gene Variants in Personality Traits. Neuropsychobiology. 59(1). 23–27. 4 indexed citations
11.
Giegling, Ina, Daniel Moreno‐De‐Luca, Dan Rujescu, et al.. (2007). Dopa decarboxylase and tyrosine hydroxylase gene variants in suicidal behavior. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(3). 308–315. 14 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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