Andrés Moreno-De-Luca

3.3k total citations
24 papers, 1.1k citations indexed

About

Andrés Moreno-De-Luca is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Andrés Moreno-De-Luca has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Psychiatry and Mental health. Recurrent topics in Andrés Moreno-De-Luca's work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Andrés Moreno-De-Luca is often cited by papers focused on Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Andrés Moreno-De-Luca collaborates with scholars based in United States, United Kingdom and France. Andrés Moreno-De-Luca's co-authors include David H. Ledbetter, Christa Lese Martin, Scott M. Myers, David W. Evans, Thomas D. Challman, Daniel Moreno‐De‐Luca, Avanti Gokhale, Victor Faúndez, Ariana P. Mullin and John L. Waddington and has published in prestigious journals such as JAMA, Journal of Neuroscience and Brain.

In The Last Decade

Andrés Moreno-De-Luca

22 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrés Moreno-De-Luca United States	14	472	298	285	269	177	24	1.1k
Ryoichi Sakuta Japan	22	408 0.9×	841 2.8×	256 0.9×	359 1.3×	299 1.7×	59	1.7k
Dawna D. Armstrong United States	21	754 1.6×	730 2.4×	510 1.8×	167 0.6×	195 1.1×	33	1.6k
Sabrina Buoni Italy	20	745 1.6×	611 2.1×	312 1.1×	235 0.9×	174 1.0×	56	1.4k
Izabela Kuchna United States	19	541 1.1×	507 1.7×	518 1.8×	147 0.5×	148 0.8×	37	1.5k
Myriam Srour Canada	20	653 1.4×	703 2.4×	197 0.7×	154 0.6×	466 2.6×	88	1.9k
Maria T. Acosta United States	20	253 0.5×	386 1.3×	333 1.2×	273 1.0×	95 0.5×	63	1.3k
Irina Zaharieva United Kingdom	13	495 1.0×	536 1.8×	261 0.9×	329 1.2×	45 0.3×	20	1.1k
Hagit Flusser Israel	20	255 0.5×	533 1.8×	306 1.1×	156 0.6×	115 0.6×	46	1.3k
Teresa Temudo Portugal	16	413 0.9×	299 1.0×	263 0.9×	291 1.1×	85 0.5×	51	1.0k
Myriam Peyrard‐Janvid Sweden	22	619 1.3×	395 1.3×	369 1.3×	128 0.5×	68 0.4×	32	1.5k

Countries citing papers authored by Andrés Moreno-De-Luca

Since Specialization

Citations

This map shows the geographic impact of Andrés 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 Andrés 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 Andrés Moreno-De-Luca more than expected).

Fields of papers citing papers by Andrés Moreno-De-Luca

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrés Moreno-De-Luca

This figure shows the co-authorship network connecting the top 25 collaborators of Andrés Moreno-De-Luca. A scholar is included among the top collaborators of Andrés 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 Andrés Moreno-De-Luca. Andrés Moreno-De-Luca 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

Oetjens, Matthew T., Alexander S. F. Berry, Andrés Moreno-De-Luca, et al.. (2025). Monogenic disorders associated with motor speech phenotypes in children and adolescents undergoing clinical exome sequencing. Genetics in Medicine. 27(4). 101374–101374. 2 indexed citations

Allington, Garrett, Neel H. Mehta, Evan Dennis, et al.. (2024). De novo variants disrupt an LDB1 -regulated transcriptional network in congenital ventriculomegaly. Brain. 148(5). 1817–1828.

Mehta, Neel H., et al.. (2023). Molecular Diagnostic Yield of Exome Sequencing in Patients With Congenital Hydrocephalus. JAMA Network Open. 6(11). e2343384–e2343384. 7 indexed citations

Hu, Yirui, Scott M. Myers, Brenda Finucane, et al.. (2023). Diagnostic Yield of Exome Sequencing in Cerebral Palsy and Implications for Genetic Testing Guidelines: A Systematic Review and Meta-analysis. Obstetrical & Gynecological Survey. 78(11). 638–639. 3 indexed citations

Hu, Yirui, Scott M. Myers, Brenda Finucane, et al.. (2023). Diagnostic Yield of Exome Sequencing in Cerebral Palsy and Implications for Genetic Testing Guidelines. JAMA Pediatrics. 177(5). 472–472. 38 indexed citations

Taylor, Cora, Brenda Finucane, Andrés Moreno-De-Luca, et al.. (2022). Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome. Genetics in Medicine. 25(1). 151–154. 6 indexed citations

Nagy, Sara, Ehsan Ghayoor Karimiani, Bobby G. Ng, et al.. (2022). A recurrent homozygous missense DPM3 variant leads to muscle and brain disease. Clinical Genetics. 102(6). 530–536. 5 indexed citations

Savatt, Juliann M., Hermela Shimelis, Andrés Moreno-De-Luca, et al.. (2022). Frequency of truncating FLCN variants and Birt-Hogg-Dubé–associated phenotypes in a health care system population. Genetics in Medicine. 24(9). 1857–1866. 14 indexed citations

Moreno-De-Luca, Andrés, Francisca Millan, Houda Zghal Elloumi, et al.. (2021). Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy. Obstetrical & Gynecological Survey. 76(7). 399–401.

10.

Moreno-De-Luca, Andrés, Francisca Millan, Houda Zghal Elloumi, et al.. (2021). Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy. JAMA. 325(5). 467–467. 71 indexed citations

11.

Wain, Karen E., Catherine Hajek, Juvianee Estrada‐Veras, et al.. (2020). Expanding the Phenotype of TUBB2A-Related Tubulinopathy: Three Cases of a Novel, Heterozygous TUBB2A Pathogenic Variant p.Gly98Arg. Molecular Syndromology. 12(1). 33–40. 8 indexed citations

12.

Siegler, James E., et al.. (2019). Carotid artery atherosclerosis is not associated with hyoid proximity: Results from a cross-sectional and longitudinal cohort study. Clinical Imaging. 58. 39–45. 4 indexed citations

13.

Evans, David W., et al.. (2014). Social cognition and neural substrates of face perception: Implications for neurodevelopmental and neuropsychiatric disorders. Behavioural Brain Research. 263. 1–8. 26 indexed citations

14.

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

15.

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

16.

Mullin, Ariana P., et al.. (2013). Neurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes. Translational Psychiatry. 3(12). e329–e329. 101 indexed citations

17.

Moreno-De-Luca, Andrés, Scott M. Myers, Thomas D. Challman, et al.. (2013). Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence. The Lancet Neurology. 12(4). 406–414. 216 indexed citations

18.

Moreno-De-Luca, Andrés, David H. Ledbetter, & Christa Lese Martin. (2012). Genetic insights into the causes and classification of the cerebral palsies. The Lancet Neurology. 11(3). 283–292. 106 indexed citations

19.

Gokhale, Avanti, Jennifer Larimore, Erica Werner, et al.. (2012). Quantitative Proteomic and Genetic Analyses of the Schizophrenia Susceptibility Factor Dysbindin Identify Novel Roles of the Biogenesis of Lysosome-Related Organelles Complex 1. Journal of Neuroscience. 32(11). 3697–3711. 74 indexed citations

20.

Moreno-De-Luca, Andrés, S. L. Helmers, Hui Mao, et al.. (2010). Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability. Journal of Medical Genetics. 48(2). 141–144. 128 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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