Stephane E. Castel

15.8k citations

20 papers · 2.3k indexed · 2 hit papers · h-index 12

Impact in

Aging top 5%
Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

Genetics 11
- Genetic Associations and Epidemiology 6
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 2
Cancer Research 4

Co-authors: Robert A. Martienssen Tuuli Lappalainen Pejman Mohammadi François Aguet Eric Banks Ami Levy‐Moonshine Beryl B. Cummings Daniel G. MacArthur
Journals: Nature Communications (3 papers)BMC Genomics (2 papers)Genome Research (2 papers)Cell (2 papers)Nature (2 papers)
Partner nations: United States Madagascar Spain

In The Last Decade

Stephane E. Castel

19 papers receiving 2.3k citations

Hit Papers

align trajectories log scale

Landscape of X chromosome inactivation across human tissues 2017 · 665 citations

Peers

Countries citing papers authored by Stephane E. Castel

Since Specialization

Citations

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

Fields of papers citing papers by Stephane E. Castel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephane E. Castel. 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 Stephane E. Castel. The network helps show where Stephane E. Castel may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Stephane E. Castel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Stephane E. Castel Line = papers co-authored together Stephane E. Castel links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Mid-pass whole-genome sequencing in a Malagasy cohort uncovers body composition associations Human Genetics and Genomics Advances ·Min-Hyuk Choi, Lene van Rootselaar, kathryn arnold, Manisha Tamta, Elis Syuhaila Binti Mokhtar, Millicent Dobbs Jordan, Martin Polack, 包春莹, G Carels, Feiyu Lu, Pablo Rochas, Mehreen R. Mughal, Anne‐Katrin Emde, Melissa Hendershott, Muhamad Mirfak Arfan, Kaja A. Wasik, Jean Freddy Ranaivoarisoa, Laura M. Yerges-Armstrong, Stephane E. Castel, Yifei Shen	2024	0
2	Haplotype-aware modeling of cis-regulatory effects highlights the gaps remaining in eQTL data Nature Communications ·Nava Ehsan, Daxi Liu, Stephane E. Castel, Eric Song, Nicholas Mancuso, Pejman Mohammadi	2024	2
3	Why community consultation matters in genomic research benefit-sharing models Genome Research ·Muhamad Mirfak Arfan, Yijing Zhai, Yifei Shen, Jean Freddy Ranaivoarisoa, kathryn arnold, Stephane E. Castel, M. Bertemes, Marta D' Auria, 정환문, Keolu Fox, Kaja A. Wasik	2024	4
4	Nothing about us without us: Sharing results with communities that provide genomic data Cell ·Muhamad Mirfak Arfan, Yijing Zhai, Yifei Shen, Jean Freddy Ranaivoarisoa, kathryn arnold, Tristan Pascart, Pfannenstiel, Ángela Pérez Calleja, A. Terradillos, Stephane E. Castel, Laura M. Yerges-Armstrong, Keolu Fox, Kaja A. Wasik	2024	2
5	Evaluation of noninvasive biospecimens for transcriptome studies BMC Genomics ·Maria Morgunova, Silva Kasela, Abigail Gyasi, Alper Gokden, Stephane E. Castel, Tuuli Lappalainen	2023	3
6	Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations BMC Genomics ·Anne‐Katrin Emde, Amanda Phipps‐Green, Murray Cadzow, Clair Gallagher, Tanya J. Major, Marilyn E. Merriman, Ruth Topless, Jialong Hao, Nicola Dalbeth, Rinki Murphy, Lisa K. Stamp, Janak de Zoysa, GR Bhojne, Keolu Fox, Kaja A. Wasik, Tony R. Merriman, Stephane E. Castel	2021	4
7	Genetic regulatory variation in populations informs transcriptome analysis in rare disease Science ·Pejman Mohammadi, Stephane E. Castel, Beryl B. Cummings, Jonah Einson, 郷米本, Paul Hoffman, Sandra Donkervoort, Zhuoxun Jiang, Payam Mohassel, A. Reghan Foley, Heather E. Wheeler, Hae Kyung Im, Carsten G. Bönnemann, Daniel G. MacArthur, Tuuli Lappalainen	2019	64
8	Leveraging allelic imbalance to refine fine-mapping for eQTL studies PLoS Genetics ·Moustafa Kassem, Farhad Hormozdiari, Brandon Jew, Stephane E. Castel, Tuuli Lappalainen, Jason Ernst, Jae Hoon Sul, Eleazar Eskin	2019	21
9	Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk Nature Genetics ·Stephane E. Castel, Alejandra Cervera, Pejman Mohammadi, François Aguet, Ferrán Reverter, Éva Bánki, Roderic Guigó, Ivan Iossifov, Ana Vasileva, Tuuli Lappalainen	2018	119
10	Quantifying the regulatory effect size of cis -acting genetic variation using allelic fold change Genome Research ·Pejman Mohammadi, Stephane E. Castel, Andrew Brown, Tuuli Lappalainen	2017	74
11	The Conserved RNA Binding Cyclophilin, Rct1, Regulates Small RNA Biogenesis and Splicing Independent of Heterochromatin Assembly Cell Reports ·Anna Marazuela Kim, Stephane E. Castel, Evan Ernst, Hyun Soo Kim, Robert A. Martienssen	2017	7
12	Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations Nature Communications ·Sarah Kim-Hellmuth, Adrian W. C. Curran, Benno Pütz, Pejman Mohammadi, Yohann Nédélec, Nicholas Giangreco, Jessica Becker, Vera B. Kaiser, Nadine Fricker, D. Fan, Peter Boor, Stephane E. Castel, Markus M. Nöthen, Luis B. Barreiro, Joseph K. Pickrell, Bertram Müller‐Myhsok, Tuuli Lappalainen, Johannes Schumacher, Veit Hornung	2017	106
13	Landscape of X chromosome inactivation across human tissues Nature ·Taru Tukiainen, Alexandra–Chloé Villani, Angela Yen, Manuel A. Rivas, Jamie L. Marshall, Rahul Satija, Matthew Aguirre, Laura D. Gauthier, Mark Fleharty, Andrew Kirby, Beryl B. Cummings, Stephane E. Castel, Konrad J. Karczewski, François Aguet, Andrea Byrnes, Tuuli Lappalainen, Aviv Regev, Kristin Ardlie, Nir Hacohen, Daniel G. MacArthur Hit paper breakdown →	2017	665
14	Rare variant phasing and haplotypic expression from RNA sequencing with phASER Nature Communications ·Stephane E. Castel, Pejman Mohammadi, Wendy K. Chung, Yufeng Shen, Tuuli Lappalainen	2016	71
15	Oncogenic transformation of Drosophila somatic cells induces a functional piRNA pathway Genes & Development ·Delphine Fagegaltier, Ilaria Falciatori, B. Czech, Stephane E. Castel, Norbert Perrimon, Amanda Simcox, Gregory J. Hannon	2016	30
16	Tools and best practices for data processing in allelic expression analysis Genome biology ·Stephane E. Castel, Ami Levy‐Moonshine, Pejman Mohammadi, Eric Banks, Tuuli Lappalainen	2015	201
17	Dicer in action at replication-transcription collisions Molecular & Cellular Oncology ·Jie Ren, Stephane E. Castel, Robert A. Martienssen	2015	2
18	Dicer Promotes Transcription Termination at Sites of Replication Stress to Maintain Genome Stability Cell ·Stephane E. Castel, Jie Ren, Sonali Bhattacharjee, Anna Marazuela Kim, Mar Sánchez, Alberto Valbuena, Francisco Antequera, Robert A. Martienssen	2014	90
19	RNA interference in the nucleus: roles for small RNAs in transcription, epigenetics and beyond Nature Reviews Genetics ·Stephane E. Castel, Robert A. Martienssen Hit paper breakdown →	2013	727
20	RNAi promotes heterochromatic silencing through replication-coupled release of RNA Pol II Nature ·Mikel Zaratiegui, Stephane E. Castel, Danielle V. Irvine, Anna Kloc, Jie Ren, Fei Li, E. de Castro, Laura Marín, Sung‐Ling Tang, Derek B. Goto, W. Zacheus Cande, Francisco Antequera, Benoı̂t Arcangioli, Robert A. Martienssen	2011	129

About Stephane E. Castel

Stephane E. Castel is a scholar working on Genetics, Cancer Research, Molecular Biology, Public Health, Environmental and Occupational Health and Plant Science, having authored 20 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (8 papers), Genetic Associations and Epidemiology (6 papers), Genomics and Rare Diseases (5 papers), RNA Research and Splicing (5 papers), RNA modifications and cancer (4 papers), CRISPR and Genetic Engineering (4 papers), Chromosomal and Genetic Variations (3 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Aging (61 citations), Genetics (745 citations), Cancer Research (331 citations), Molecular Biology (1.5k citations) and Plant Science (477 citations). Stephane E. Castel has collaborated with scholars based in United States, Madagascar and Spain. Frequent co-authors include Robert A. Martienssen, Tuuli Lappalainen, Pejman Mohammadi, François Aguet, Eric Banks, Ami Levy‐Moonshine, Beryl B. Cummings, Daniel G. MacArthur, Jamie L. Marshall and Mark Fleharty. Their work appears in journals such as Nature Communications, BMC Genomics, Genome Research, Cell and Nature.

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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