Dalila Pinto

36.1k total citations
46 papers, 3.1k citations indexed

About

Dalila Pinto is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Dalila Pinto has authored 46 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Genetics, 14 papers in Cognitive Neuroscience and 13 papers in Molecular Biology. Recurrent topics in Dalila Pinto's work include Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Autism Spectrum Disorder Research (13 papers). Dalila Pinto is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Autism Spectrum Disorder Research (13 papers). Dalila Pinto collaborates with scholars based in United States, Canada and United Kingdom. Dalila Pinto's co-authors include Stephen W. Scherer, Christian R. Marshall, Péter Szatmári, Wendy Roberts, James S. Sutcliffe, Rainald Moessner, Lonnie Zwaigenbaum, Bridget A. Fernandez, Jennifer Skaug and John B. Vincent and has published in prestigious journals such as Nature Communications, Nature Genetics and PLoS ONE.

In The Last Decade

Dalila Pinto

45 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dalila Pinto United States	23	2.0k	1.4k	882	374	263	46	3.1k
Michael E. Talkowski United States	32	1.9k 0.9×	2.7k 1.9×	489 0.6×	324 0.9×	323 1.2×	100	4.3k
Dag H. Yasui United States	32	1.9k 0.9×	2.4k 1.7×	792 0.9×	297 0.8×	225 0.9×	46	3.5k
Nicholas J. Bray United Kingdom	31	1.5k 0.8×	2.1k 1.5×	525 0.6×	551 1.5×	149 0.6×	62	3.5k
Jonathan L. Haines United States	35	1.7k 0.8×	1.6k 1.2×	1.1k 1.3×	469 1.3×	202 0.8×	66	4.2k
Hyejung Won United States	21	2.1k 1.1×	2.3k 1.6×	1.4k 1.6×	518 1.4×	134 0.5×	45	4.0k
Irina Voineagu Australia	18	1.3k 0.6×	2.3k 1.7×	994 1.1×	440 1.2×	256 1.0×	34	3.3k
Jennifer K. Lowe United States	26	2.6k 1.3×	2.6k 1.9×	1.8k 2.1×	434 1.2×	260 1.0×	48	5.3k
Christian R. Marshall Canada	39	3.2k 1.6×	2.8k 2.1×	1.2k 1.3×	501 1.3×	441 1.7×	142	5.4k
Luis de la Torre-Ubieta United States	22	1.2k 0.6×	2.3k 1.7×	680 0.8×	355 0.9×	246 0.9×	29	3.3k
Santhosh Girirajan United States	34	3.4k 1.7×	2.5k 1.8×	1.0k 1.2×	399 1.1×	251 1.0×	82	5.0k

Countries citing papers authored by Dalila Pinto

Since Specialization

Citations

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

Fields of papers citing papers by Dalila Pinto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dalila Pinto

This figure shows the co-authorship network connecting the top 25 collaborators of Dalila Pinto. A scholar is included among the top collaborators of Dalila Pinto 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 Dalila Pinto. Dalila Pinto 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

Dai, Rujia, Ming Zhang, Xuan Wang, et al.. (2024). Evaluating performance and applications of sample-wise cell deconvolution methods on human brain transcriptomic data. Science Advances. 10(21). eadh2588–eadh2588. 6 indexed citations

Luo, Jie, Ling Li, Dehui Kong, et al.. (2024). Genetic regulation of human brain proteome reveals proteins implicated in psychiatric disorders. Molecular Psychiatry. 29(11). 3330–3343. 7 indexed citations

Dobbyn, Amanda, Ruth C. Brown, Brien P. Riley, et al.. (2020). mTADA is a framework for identifying risk genes from de novo mutations in multiple traits. Nature Communications. 11(1). 2929–2929. 17 indexed citations

Ascencio-Montiel, Iván de Jesús, Dalila Pinto, Esteban J. Parra, et al.. (2017). Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjects. Scientific Reports. 7(1). 17105–17105. 6 indexed citations

Breen, Michael S., Anne Uhlmann, Süreyya Özcan, et al.. (2017). Parallel changes in serum proteins and diffusion tensor imaging in methamphetamine-associated psychosis. Scientific Reports. 7(1). 43777–43777. 8 indexed citations

Merikangas, Alison, Ricardo Segurado, Elizabeth A. Heron, et al.. (2014). The phenotypic manifestations of rare genic CNVs in autism spectrum disorder. Molecular Psychiatry. 20(11). 1366–1372. 23 indexed citations

Uddin, Mohammed, Kristiina Tammimies, Giovanna Pellecchia, et al.. (2014). Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder. Nature Genetics. 46(7). 742–747. 98 indexed citations

Noh, Hyun Ji, Chris P. Ponting, Stephen Meader, et al.. (2013). Network Topologies and Convergent Aetiologies Arising from Deletions and Duplications Observed in Individuals with Autism. PLoS Genetics. 9(6). e1003523–e1003523. 42 indexed citations

Nishiyama, Takeshi, Kunihiko Takahashi, Toshiro Tango, et al.. (2011). A scan statistic to extract causal gene clusters from case-control genome-wide rare CNV data. BMC Bioinformatics. 12(1). 205–205. 3 indexed citations

10.

Wintle, Richard F., Anath C. Lionel, Pingzhao Hu, et al.. (2011). A genotype resource for postmortem brain samples from the Autism Tissue Program. Autism Research. 4(2). 89–97. 21 indexed citations

11.

Vieland, Veronica J., Joachim Hallmayer, Yungui Huang, et al.. (2011). Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. Journal of Neurodevelopmental Disorders. 3(2). 113–123. 16 indexed citations

12.

Choufani, Sanaa, Jonathan Shapiro, Martha Susiarjo, et al.. (2011). A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes. Genome Research. 21(3). 465–476. 89 indexed citations

13.

Pang, Andy Wing Chun, Jeffrey R. MacDonald, Dalila Pinto, et al.. (2010). Towards a comprehensive structural variation map of an individual human genome. Genome biology. 11(5). R52–R52. 214 indexed citations

14.

Kovel, Carolien G. F. de, Dalila Pinto, Ulrike Tauer, et al.. (2010). Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis. Epilepsy Research. 89(2-3). 286–294. 33 indexed citations

15.

Pagnamenta, A. T., Hamza Khan, Susan Walker, et al.. (2010). Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Journal of Medical Genetics. 48(1). 48–54. 76 indexed citations

16.

Bigham, Abigail W., Marc Bauchet, Dalila Pinto, et al.. (2010). Identifying Signatures of Natural Selection in Tibetan and Andean Populations Using Dense Genome Scan Data. PLoS Genetics. 6(9). e1001116–e1001116. 430 indexed citations

17.

Monsuur, Alienke J., Paul I. W. de Bakker, Alexandra Zhernakova, et al.. (2008). Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms. PLoS ONE. 3(5). e2270–e2270. 117 indexed citations

18.

Haan, Gerrit‐Jan de, et al.. (2006). Oligogenic inheritance in photosensitive juvenile myoclonic epilepsy?. Epileptic Disorders. 8(1). 32–36. 3 indexed citations

19.

Stephani, Ulrich, Ulrike Tauer, Bobby P.C. Koeleman, et al.. (2004). Genetics of Photosensitivity (Photoparoxysmal Response): A Review. Epilepsia. 45(s1). 19–23. 65 indexed citations

20.

Pinto, Dalila, Gerrit‐Jan de Haan, Eduard H. Boezeman, et al.. (2004). Evidence for Linkage between Juvenile Myoclonic Epilepsy–Related Idiopathic Generalized Epilepsy and 6p11‐12 in Dutch Families. Epilepsia. 45(3). 211–217. 22 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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