Author

Sachin Desai

Hospital for Sick Children

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Ecology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:ecology & biodiversity· 1 Approach:experimental assay· 1 Assay:field survey / ecological data· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ada J. S. Chan· 1 shared Afiqah YusufiD· 1 shared Akshay Mandavkar· 1 shared Alana Iaboni· 1 shared Amruta JoglekariD· 1 shared Ankur A. PatwardhaniD· 1 shared Annabel Rutherford· 1 shared Anup Bokkasa· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ada J. S. Chan

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2 papers

Recent·Most cited

Understudied and underprotected: biodiversity and conservation challenges in the Konkan region of Maharashtra

Kruti S. Chhaya, Gurudas V. Nulkar, Parth Bapat, Hrushikesh Barve, Nupur Bhave, Anup Bokkasa, Vaidehi Dandekar, Sachin Desai, Ketaki Ghate, Revati Gindi, Amruta Joglekar, Atul Joshi, Poorva Joshi, Satish Kamat, Manasi Karandikar, , Rohit Naniwadekar

This study identifies knowledge gaps and conservation challenges in the Konkan region of Maharashtra through literature review and focus group discussions, highlighting threats like land-use change and climate change impacts.

bioRxiv · May 16, 2025 · PreprintEcology

Genomic architecture of autism spectrum disorder from comprehensive whole-genome sequence annotation

Brett Trost, Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe, Livia Oliveira Loureiro, Miriam S. Reuter, Delnaz Roshandel, Joe Whitney, Mehdi Zarrei, Matthew Bookman, Cherith Somerville, Rulan Shaath, Mona Abdi, , Evdokia A. Anagnostou

This study identifies 135 ASD-associated protein-coding genes using whole-genome sequencing data from 11,312 individuals and exome sequencing from over 18,000 trios, with a false discovery rate of 80%.

medRxiv · May 5, 2022 · PreprintGenetic & Genomic Medicine