Sebastian Akle

404 total citations
7 papers, 253 citations indexed

About

Sebastian Akle is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Sebastian Akle has authored 7 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 1 paper in Genetics. Recurrent topics in Sebastian Akle's work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Genetic Associations and Epidemiology (2 papers). Sebastian Akle is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Genetic Associations and Epidemiology (2 papers). Sebastian Akle collaborates with scholars based in United States, Australia and Germany. Sebastian Akle's co-authors include Virginia M.‐Y. Lee, Murray Grossman, Johanna Busch, Laura A. Volpicelli‐Daley, John Q. Trojanowski, Travis L. Unger, Vivianna M. Van Deerlin, Linda K. Kwong, Alice Chen‐Plotkin and Michael D. Gallagher and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Sebastian Akle

7 papers receiving 250 citations

Peers

Countries citing papers authored by Sebastian Akle

Since Specialization

Citations

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

Fields of papers citing papers by Sebastian Akle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sebastian Akle

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits 2022 ·PLoS Genetics ·Sung Chun, Sebastian Akle, Athanasios Teodosiadis, Brian E. Cade, Heming Wang, Tamar Sofer, Daniel S. Evans, Katie L. Stone, Sina A. Gharib, Sutapa Mukherjee, Lyle J. Palmer, David R. Hillman, Jerome I. Rotter, Craig L. Hanis, J Stamatoyannopoulos, Susan Redline, Chris Cotsapas, Shamil Sunyaev	8
2	Purifying selection on noncoding deletions of human regulatory loci detected using their cellular pleiotropy 2021 ·Genome Research ·(unknown), Jae Hoon Sul, Daniel J. Balick, Sebastian Akle, (unknown), Robert C. Green, Shamil Sunyaev	5
3	Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy 2020 ·Nature Genetics ·Maria Kousi, Onuralp Söylemez, (unknown), Niki Mourtzi, Sebastian Akle, Irwin Jungreis, Jean Muller, Christopher A. Cassa, Harrison Brand, Jill A. Rosenfeld, Maxim Y. Wolf, Azita Sadeghpour, (unknown), Richard A. Lewis, Michael E. Talkowski, Hélène Dollfus, Manolis Kellis, Erica E. Davis, Shamil Sunyaev, Nicholas Katsanis	21
4	Fetal alcohol spectrum disorder predisposes to metabolic abnormalities in adulthood 2020 ·Journal of Clinical Investigation ·Olivia Weeks, Gabriel D. Bossé, Isaac M. Oderberg, Sebastian Akle, Yariv Houvras, Paul J. Wrighton, Kyle A. LaBella, (unknown), Sahar Tavakoli, Isaac Adatto, (unknown), Daan J. Kloosterman, (unknown), Michael E. Charness, Randall T. Peterson, Matthew L. Steinhauser, Pouneh K. Fazeli, Wolfram Goessling	36
5	When “N of 2” is not enough: integrating statistical and functional data in gene discovery 2017 ·Molecular Case Studies ·Christopher A. Cassa, Sebastian Akle, Daniel M. Jordan, Jill A. Rosenfeld	1
6	Mitigating False-Positive Associations in Rare Disease Gene Discovery 2015 ·Human Mutation ·Sebastian Akle, Sung Chun, Daniel M. Jordan, Christopher A. Cassa	11
7	TMEM106B, the Risk Gene for Frontotemporal Dementia, Is Regulated by the microRNA-132/212 Cluster and Affects Progranulin Pathways 2012 ·Journal of Neuroscience ·Alice Chen‐Plotkin, Travis L. Unger, Michael D. Gallagher, (unknown), Linda K. Kwong, Laura A. Volpicelli‐Daley, Johanna Busch, Sebastian Akle, Murray Grossman, Vivianna M. Van Deerlin, John Q. Trojanowski, Virginia M.‐Y. Lee	171

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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