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BMC Medical Genomics
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October 30, 2023
Genome-wide neonatal epigenetic changes associated with maternal exposure to the COVID-19 pandemic
Kristen Kocher, Surajit Bhattacharya, Nickie Niforatos-Andescavage, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 12, 2026
Kauro, a graph-based chatbot for high-fidelity information transmission conversations
Charles Hadley King, Rebekah Barrick, Miguel Almalvez, et al.
Genome Medicine
|
October 27, 2017
Next-generation mapping: a novel approach for detection of pathogenic structural variants with a potential utility in clinical diagnosis
Hayk Barseghyan, Wilson Tang, Richard T Wang, et al.
Biology of Sex Differences
|
January 31, 2018
Identification of novel candidate genes for 46,XY disorders of sex development (DSD) using a C57BL/6J-Y <sup>POS</sup> mouse model
Hayk Barseghyan, Aleisha Symon, Mariam Zadikyan, et al.
The Journal of Pathology
|
May 19, 2023
Optical genome mapping identifies a novel pediatric embryonal tumor with a ZNF532::NUTM1 fusion
Miriam Bornhorst, Augustine Eze, Surajit Bhattacharya, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 24, 2025
Long-read sequencing resolves the clinically relevant <i>CYP21A2</i> locus, supporting a new clinical test for Congenital Adrenal Hyperplasia
Jean Monlong, Xiao Chen, Hayk Barseghyan, et al.
Genome Research
|
March 9, 2019
Long-read single-molecule maps of the functional methylome
Hila Sharim, Assaf Grunwald, Tslil Gabrieli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 10, 2025
Genome sequencing reveals the impact of pseudoexons in rare genetic disease
Georgia Pitsava, Megan Hawley, Light Auriga, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 7, 2025
Genome sequencing reveals the impact of non-canonical exon inclusions in rare genetic disease
Georgia Pitsava, Megan Hawley, Light Auriga, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
BMC Medical Genomics
|
October 30, 2023
Genome-wide neonatal epigenetic changes associated with maternal exposure to the COVID-19 pandemic
Kristen Kocher, Surajit Bhattacharya, Nickie Niforatos-Andescavage, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 12, 2026
Kauro, a graph-based chatbot for high-fidelity information transmission conversations
Charles Hadley King, Rebekah Barrick, Miguel Almalvez, et al.
Genome Medicine
|
October 27, 2017
Next-generation mapping: a novel approach for detection of pathogenic structural variants with a potential utility in clinical diagnosis
Hayk Barseghyan, Wilson Tang, Richard T Wang, et al.
Biology of Sex Differences
|
January 31, 2018
Identification of novel candidate genes for 46,XY disorders of sex development (DSD) using a C57BL/6J-Y <sup>POS</sup> mouse model
Hayk Barseghyan, Aleisha Symon, Mariam Zadikyan, et al.
The Journal of Pathology
|
May 19, 2023
Optical genome mapping identifies a novel pediatric embryonal tumor with a ZNF532::NUTM1 fusion
Miriam Bornhorst, Augustine Eze, Surajit Bhattacharya, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 24, 2025
Long-read sequencing resolves the clinically relevant <i>CYP21A2</i> locus, supporting a new clinical test for Congenital Adrenal Hyperplasia
Jean Monlong, Xiao Chen, Hayk Barseghyan, et al.
Genome Research
|
March 9, 2019
Long-read single-molecule maps of the functional methylome
Hila Sharim, Assaf Grunwald, Tslil Gabrieli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 10, 2025
Genome sequencing reveals the impact of pseudoexons in rare genetic disease
Georgia Pitsava, Megan Hawley, Light Auriga, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 7, 2025
Genome sequencing reveals the impact of non-canonical exon inclusions in rare genetic disease
Georgia Pitsava, Megan Hawley, Light Auriga, et al.
Page
of 1