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Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Modelling DNA replication fork stability and collapse using chromatin fiber analysis and the R-ODD-BLOBS program
Kerenza Cheng, Kazeera Aliar, Roozbeh Manshaei, et al.
NPJ Genomic Medicine
|
February 22, 2024
A call for increased inclusivity and global representation in pharmacogenetic testing
April Kennedy, Gabriel Ma, Roozbeh Manshaei, et al.
ISRN Bioinformatics
|
May 14, 2015
Hybrid-controlled neurofuzzy networks analysis resulting in genetic regulatory networks reconstruction
Roozbeh Manshaei, Pooya Sobhe Bidari, Mahdi Aliyari Shoorehdeli, et al.
Translational Psychiatry
|
February 2, 2021
Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia
Bahareh A Mojarad, Yue Yin, Roozbeh Manshaei, et al.
BMC Medical Genomics
|
February 19, 2022
GeneTerpret: a customizable multilayer approach to genomic variant prioritization and interpretation
Roozbeh Manshaei, Sean DeLong, Veronica Andric, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 27, 2022
Trio genome sequencing for developmental delay and pediatric heart conditions: A comparative microcost analysis
Jathishinie Jegathisawaran, Kate Tsiplova, Robin Z Hayeems, et al.
JAMA Network Open
|
May 26, 2021
Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting
Iris Cohn, Roozbeh Manshaei, Eriskay Liston, et al.
Human Genetics
|
November 15, 2022
SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing
Qiliang Ding, Cherith Somerville, Roozbeh Manshaei, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 21, 2018
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot
Miriam S Reuter, Rebekah Jobling, Rajiv R Chaturvedi, et al.
Frontiers in Genetics
|
October 28, 2020
Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences
Roozbeh Manshaei, Daniele Merico, Miriam S Reuter, et al.
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of 2
Search research articles
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Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
Modelling DNA replication fork stability and collapse using chromatin fiber analysis and the R-ODD-BLOBS program
Kerenza Cheng, Kazeera Aliar, Roozbeh Manshaei, et al.
NPJ Genomic Medicine
|
February 22, 2024
A call for increased inclusivity and global representation in pharmacogenetic testing
April Kennedy, Gabriel Ma, Roozbeh Manshaei, et al.
ISRN Bioinformatics
|
May 14, 2015
Hybrid-controlled neurofuzzy networks analysis resulting in genetic regulatory networks reconstruction
Roozbeh Manshaei, Pooya Sobhe Bidari, Mahdi Aliyari Shoorehdeli, et al.
Translational Psychiatry
|
February 2, 2021
Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia
Bahareh A Mojarad, Yue Yin, Roozbeh Manshaei, et al.
BMC Medical Genomics
|
February 19, 2022
GeneTerpret: a customizable multilayer approach to genomic variant prioritization and interpretation
Roozbeh Manshaei, Sean DeLong, Veronica Andric, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 27, 2022
Trio genome sequencing for developmental delay and pediatric heart conditions: A comparative microcost analysis
Jathishinie Jegathisawaran, Kate Tsiplova, Robin Z Hayeems, et al.
JAMA Network Open
|
May 26, 2021
Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting
Iris Cohn, Roozbeh Manshaei, Eriskay Liston, et al.
Human Genetics
|
November 15, 2022
SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing
Qiliang Ding, Cherith Somerville, Roozbeh Manshaei, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 21, 2018
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot
Miriam S Reuter, Rebekah Jobling, Rajiv R Chaturvedi, et al.
Frontiers in Genetics
|
October 28, 2020
Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences
Roozbeh Manshaei, Daniele Merico, Miriam S Reuter, et al.
Page
of 2