Rohan V Patel
Overview
Explore the profile of Rohan V Patel including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
12
Citations
850
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Fehlings D, Zarrei M, Engchuan W, Sondheimer N, Thiruvahindrapuram B, MacDonald J, et al.
Nat Genet
. 2024 Mar;
56(4):585-594.
PMID: 38553553
We performed whole-genome sequencing (WGS) in 327 children with cerebral palsy (CP) and their biological parents. We classified 37 of 327 (11.3%) children as having pathogenic/likely pathogenic (P/LP) variants and...
2.
Mastromatteo S, Chen A, Gong J, Lin F, Thiruvahindrapuram B, Sung W, et al.
HGG Adv
. 2022 Nov;
4(1):100156.
PMID: 36386424
Phasing of heterozygous alleles is critical for interpretation of -effects of disease-relevant variation. We sequenced 477 individuals with cystic fibrosis (CF) using linked-read sequencing, which display an average phase block...
3.
Trost B, Thiruvahindrapuram B, Chan A, Engchuan W, Higginbotham E, Howe J, et al.
Cell
. 2022 Nov;
185(23):4409-4427.e18.
PMID: 36368308
Fully understanding autism spectrum disorder (ASD) genetics requires whole-genome sequencing (WGS). We present the latest release of the Autism Speaks MSSNG resource, which includes WGS data from 5,100 individuals with...
4.
Chan A, Engchuan W, Reuter M, Wang Z, Thiruvahindrapuram B, Trost B, et al.
Nat Commun
. 2022 Oct;
13(1):6463.
PMID: 36309498
Defining different genetic subtypes of autism spectrum disorder (ASD) can enable the prediction of developmental outcomes. Based on minor physical and major congenital anomalies, we categorize 325 Canadian children with...
5.
Zarrei M, Burton C, Engchuan W, Young E, Higginbotham E, MacDonald J, et al.
NPJ Genom Med
. 2019 Oct;
4:26.
PMID: 31602316
Copy number variations (CNVs) are implicated across many neurodevelopmental disorders (NDDs) and contribute to their shared genetic etiology. Multiple studies have attempted to identify shared etiology among NDDs, but this...
6.
Reuter M, Walker S, Thiruvahindrapuram B, Whitney J, Cohn I, Sondheimer N, et al.
CMAJ
. 2018 Feb;
190(5):E126-E136.
PMID: 29431110
Background: The Personal Genome Project Canada is a comprehensive public data resource that integrates whole genome sequencing data and health information. We describe genomic variation identified in the initial recruitment...
7.
Yuen R, Merico D, Bookman M, Howe J, Thiruvahindrapuram B, Patel R, et al.
Nat Neurosci
. 2017 Mar;
20(4):602-611.
PMID: 28263302
We are performing whole-genome sequencing of families with autism spectrum disorder (ASD) to build a resource (MSSNG) for subcategorizing the phenotypes and underlying genetic factors involved. Here we report sequencing...
8.
Patel R, Hamanishi E, Provart N
PLoS One
. 2016 Mar;
11(3):e0150982.
PMID: 26954504
Transcriptomic studies help to further our understanding of gene function. Human transcriptomic studies tend to focus on a particular subset of tissue types or a particular disease state; however, it...
9.
Righetti K, Ly Vu J, Pelletier S, Ly Vu B, Glaab E, Lalanne D, et al.
Plant Cell
. 2015 Sep;
27(10):2692-708.
PMID: 26410298
Seed longevity, the maintenance of viability during storage, is a crucial factor for preservation of genetic resources and ensuring proper seedling establishment and high crop yield. We used a systems...
10.
Wang L, Czedik-Eysenberg A, Mertz R, Si Y, Tohge T, Nunes-Nesi A, et al.
Nat Biotechnol
. 2014 Oct;
32(11):1158-65.
PMID: 25306245
C₄ and C₃ photosynthesis differ in the efficiency with which they consume water and nitrogen. Engineering traits of the more efficient C₄ photosynthesis into C₃ crops could substantially increase crop...