Alejandro Q. Nato

483 total citations
17 papers, 167 citations indexed

About

Alejandro Q. Nato is a scholar working on Genetics, Molecular Biology and Developmental and Educational Psychology. According to data from OpenAlex, Alejandro Q. Nato has authored 17 papers receiving a total of 167 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 9 papers in Molecular Biology and 2 papers in Developmental and Educational Psychology. Recurrent topics in Alejandro Q. Nato's work include Genetic Associations and Epidemiology (12 papers), Genetic and phenotypic traits in livestock (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Alejandro Q. Nato is often cited by papers focused on Genetic Associations and Epidemiology (12 papers), Genetic and phenotypic traits in livestock (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Alejandro Q. Nato collaborates with scholars based in United States, Germany and Qatar. Alejandro Q. Nato's co-authors include Ellen M. Wijsman, Wendy H. Raskind, Harkirat Sohi, Nicola H. Chapman, Tara C. Matise, Elizabeth Blue, Zoran Brkanac, Kathy Chapman, Yong Lin and James H. Millonig and has published in prestigious journals such as Bioinformatics, PLoS ONE and Genome Research.

In The Last Decade

Alejandro Q. Nato

16 papers receiving 163 citations

Peers

Alejandro Q. Nato

GENET

DEP

PMH

Gérald Bussy France

Joery den Hoed Netherlands

Watfa Al‐Mamari Oman

Mark Lathrop France

Brandon Wilk United States

James H. Schick United States

F.F. Brockschmidt Germany

Laura Covill United Kingdom

Katrin Männik Estonia

Sailaja Golla United States

Gérald Bussy France

Alejandro Q. Nato

80 ×0.8

GENET

70 ×1.3

31 ×0.9

25 ×0.9

DEP

14 ×1.6

PMH

Citations per year, relative to Alejandro Q. Nato Alejandro Q. Nato (= 1×) peers Gérald Bussy

Countries citing papers authored by Alejandro Q. Nato

Since Specialization

Citations

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

Fields of papers citing papers by Alejandro Q. Nato

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alejandro Q. Nato. 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 Alejandro Q. Nato. The network helps show where Alejandro Q. Nato may publish in the future.

Co-authorship network of co-authors of Alejandro Q. Nato

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

All Works

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17 of 17 papers shown

Horimoto, Andréa R. V. R., et al.. (2025). Genomic Exploration of Essential Hypertension in African‐Brazilian Quilombo Populations: A Comprehensive Approach With Pedigree Analysis and Family‐Based Association Studies. Journal of the American Heart Association. 14(7). e036193–e036193.

Horimoto, Andréa R. V. R., Elizabeth Blue, Kelsey Grinde, et al.. (2023). Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations. Human Genetics and Genomics Advances. 4(3). 100207–100207. 8 indexed citations

Ullah, Ehsan, Raghvendra Mall, Mostafa Abbas, et al.. (2018). Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees. Genome Research. 29(1). 125–134. 16 indexed citations

Nafikov, Rafael A., Alejandro Q. Nato, Harkirat Sohi, et al.. (2018). Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP. Genetic Epidemiology. 42(6). 500–515. 3 indexed citations

Kunji, Khalid, Ehsan Ullah, Alejandro Q. Nato, Ellen M. Wijsman, & Mohamad Saad. (2017). GIGI-Quick: a fast approach to impute missing genotypes in genome-wide association family data. Bioinformatics. 34(9). 1591–1593. 1 indexed citations

Blue, Elizabeth, Lisa Brown, Matthew P. Conomos, et al.. (2016). Estimating relationships between phenotypes and subjects drawn from admixed families. BMC Proceedings. 10(S7). 357–362. 4 indexed citations

Shriberg, Lawrence D., Kathy Chapman, Andrew K. Adams, et al.. (2016). Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders. Human Genetics. 135(12). 1329–1341. 9 indexed citations

Peter, Beate, Ellen M. Wijsman, Alejandro Q. Nato, et al.. (2016). Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. PLoS ONE. 11(4). e0153864–e0153864. 31 indexed citations

Saad, Mohamad, Alejandro Q. Nato, Steven M. Lewis, et al.. (2016). Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data. BMC Proceedings. 10(S7). 295–301. 3 indexed citations

10.

Matteson, Paul G., Alejandro Q. Nato, Yong Lin, et al.. (2015). The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation. Developmental Biology. 402(1). 17–31. 22 indexed citations

11.

Chapman, Nicola H., Alejandro Q. Nato, Raphael Bernier, et al.. (2015). Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. Human Genetics. 134(10). 1055–1068. 42 indexed citations

12.

Nato, Alejandro Q., et al.. (2015). PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers. Bioinformatics. 31(23). 3790–3798. 5 indexed citations

13.

Musolf, Anthony M., Alejandro Q. Nato, Douglas Londoño, et al.. (2014). Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities. BMC Proceedings. 8(S1). S81–S81. 5 indexed citations

14.

Londoño, Douglas, Lisheng Zhou, Jinchuan Xing, et al.. (2012). Single-Variant and Multi-Variant Trend Tests for Genetic Association with Next-Generation Sequencing That Are Robust to Sequencing Error. Human Heredity. 74(3-4). 172–183. 4 indexed citations

15.

Nato, Alejandro Q.. (2011). Genomic characterization of schizophrenia candidate gene regions. Rutgers University Community Repository (Rutgers University). 1 indexed citations

16.

Shimada, Makoto, Karuna Panchapakesan, Sarah A. Tishkoff, Alejandro Q. Nato, & Jody Hey. (2006). Divergent Haplotypes and Human History as Revealed in a Worldwide Survey of X-Linked DNA Sequence Variation. Molecular Biology and Evolution. 24(3). 687–698. 11 indexed citations

17.

Mojica, Elmer‐Rico E., et al.. (2005). Application of Irradiation as Pretreatment Method in the Production of Fermented Fish Paste. 2 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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