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Bjpsych Open
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August 17, 2022
Pharmacogenomics: an opportunity for personalised psychotropic prescribing in adults with intellectual disabilities
Bhathika Perera, Charles Steward, Ken Courtenay, et al.
Pharmaceutical Medicine
|
July 8, 2024
Increasing Diversity, Equity, Inclusion, and Accessibility in Rare Disease Clinical Trials
Gareth Baynam, Simeón Baker, Charles Steward, et al.
Plos One
|
March 13, 2026
Plasma lipidomics, choline metabolites, and metabolic-associated steatotic liver disease (MASLD): A Coronary Artery Risk Development in Young Adults (CARDIA) study
Jessica K Sprinkles, Qiyao Qin, Charles Steward, et al.
Orphanet Journal of Rare Diseases
|
September 28, 2024
Leaving no patient behind! Expert recommendation in the use of innovative technologies for diagnosing rare diseases
Clara D M van Karnebeek, Anne O'Donnell-Luria, Gareth Baynam, et al.
Genome Research
|
September 8, 2012
GENCODE: the reference human genome annotation for The ENCODE Project
Jennifer Harrow, Adam Frankish, Jose M Gonzalez, et al.
Genome Research
|
June 6, 2009
The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes
Kim D Pruitt, Jennifer Harrow, Rachel A Harte, et al.
BMC Genomics
|
May 17, 2013
Structural and functional annotation of the porcine immunome
Harry D Dawson, Jane E Loveland, Géraldine Pascal, et al.
Nature Genetics
|
October 3, 2018
Sixteen diverse laboratory mouse reference genomes define strain-specific haplotypes and novel functional loci
Jingtao Lilue, Anthony G Doran, Ian T Fiddes, et al.
Nature
|
April 21, 2006
DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage
Michael C Zody, Manuel Garber, David J Adams, et al.
Plos Biology
|
April 23, 2004
Integrative annotation of 21,037 human genes validated by full-length cDNA clones
Tadashi Imanishi, Takeshi Itoh, Yutaka Suzuki, et al.
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Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Bjpsych Open
|
August 17, 2022
Pharmacogenomics: an opportunity for personalised psychotropic prescribing in adults with intellectual disabilities
Bhathika Perera, Charles Steward, Ken Courtenay, et al.
Pharmaceutical Medicine
|
July 8, 2024
Increasing Diversity, Equity, Inclusion, and Accessibility in Rare Disease Clinical Trials
Gareth Baynam, Simeón Baker, Charles Steward, et al.
Plos One
|
March 13, 2026
Plasma lipidomics, choline metabolites, and metabolic-associated steatotic liver disease (MASLD): A Coronary Artery Risk Development in Young Adults (CARDIA) study
Jessica K Sprinkles, Qiyao Qin, Charles Steward, et al.
Orphanet Journal of Rare Diseases
|
September 28, 2024
Leaving no patient behind! Expert recommendation in the use of innovative technologies for diagnosing rare diseases
Clara D M van Karnebeek, Anne O'Donnell-Luria, Gareth Baynam, et al.
Genome Research
|
September 8, 2012
GENCODE: the reference human genome annotation for The ENCODE Project
Jennifer Harrow, Adam Frankish, Jose M Gonzalez, et al.
Genome Research
|
June 6, 2009
The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes
Kim D Pruitt, Jennifer Harrow, Rachel A Harte, et al.
BMC Genomics
|
May 17, 2013
Structural and functional annotation of the porcine immunome
Harry D Dawson, Jane E Loveland, Géraldine Pascal, et al.
Nature Genetics
|
October 3, 2018
Sixteen diverse laboratory mouse reference genomes define strain-specific haplotypes and novel functional loci
Jingtao Lilue, Anthony G Doran, Ian T Fiddes, et al.
Nature
|
April 21, 2006
DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage
Michael C Zody, Manuel Garber, David J Adams, et al.
Plos Biology
|
April 23, 2004
Integrative annotation of 21,037 human genes validated by full-length cDNA clones
Tadashi Imanishi, Takeshi Itoh, Yutaka Suzuki, et al.
Page
of 1