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Nature Communications
|
December 15, 2020
The role of polygenic risk and susceptibility genes in breast cancer over the course of life
Nina Mars, Elisabeth Widén, Sini Kerminen, et al.
The American Journal of Psychiatry
|
April 3, 2009
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
, Sven Cichon, Nick Craddock, et al.
Genes and Immunity
|
December 17, 2024
Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia
A Inkeri Lokki, Michael Triebwasser, Emma Daly, et al.
Nature Communications
|
June 10, 2022
Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci
João Fadista, Line Skotte, Juha Karjalainen, et al.
BMJ Open
|
March 9, 2017
A preconsultation web-based tool to generate an agenda for discussion in diabetes outpatient clinics to improve patient outcomes (DIAT): a feasibility study
Obioha C Ukoumunne, Bijay Vaidya, Julia Frost, et al.
BMC Research Notes
|
June 27, 2023
A chromosome scale assembly of the tarnished plant bug, Lygus lineolaris (Palisot de Beauvois), genome
O P Perera, Surya Saha, James Glover, et al.
BMJ Open
|
August 2, 2013
A pilot randomised controlled trial of a preconsultation web-based intervention to improve the care quality and clinical outcomes of diabetes outpatients (DIAT)
Julia Frost, Rob Anderson, Catherine Argyle, et al.
American Journal of Human Genetics
|
November 20, 2024
Inherited infertility: Mapping loci associated with impaired female reproduction
Sanni Ruotsalainen, Juha Karjalainen, Mitja Kurki, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
May 8, 2023
Identification of complement factor H variants that predispose to pre-eclampsia: A genetic and functional study
A Inkeri Lokki, Zhen Ren, Michael Triebwasser, et al.
Genome Research
|
December 25, 2019
Identification of pathogenic variant enriched regions across genes and gene families
Eduardo Pérez-Palma, Patrick May, Sumaiya Iqbal, et al.
Page
of 15
Search research articles
Search
Showing results (51-60 of 149) with videos related to
Sort By:
Page
of 15
Nature Communications
|
December 15, 2020
The role of polygenic risk and susceptibility genes in breast cancer over the course of life
Nina Mars, Elisabeth Widén, Sini Kerminen, et al.
The American Journal of Psychiatry
|
April 3, 2009
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
, Sven Cichon, Nick Craddock, et al.
Genes and Immunity
|
December 17, 2024
Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia
A Inkeri Lokki, Michael Triebwasser, Emma Daly, et al.
Nature Communications
|
June 10, 2022
Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci
João Fadista, Line Skotte, Juha Karjalainen, et al.
BMJ Open
|
March 9, 2017
A preconsultation web-based tool to generate an agenda for discussion in diabetes outpatient clinics to improve patient outcomes (DIAT): a feasibility study
Obioha C Ukoumunne, Bijay Vaidya, Julia Frost, et al.
BMC Research Notes
|
June 27, 2023
A chromosome scale assembly of the tarnished plant bug, Lygus lineolaris (Palisot de Beauvois), genome
O P Perera, Surya Saha, James Glover, et al.
BMJ Open
|
August 2, 2013
A pilot randomised controlled trial of a preconsultation web-based intervention to improve the care quality and clinical outcomes of diabetes outpatients (DIAT)
Julia Frost, Rob Anderson, Catherine Argyle, et al.
American Journal of Human Genetics
|
November 20, 2024
Inherited infertility: Mapping loci associated with impaired female reproduction
Sanni Ruotsalainen, Juha Karjalainen, Mitja Kurki, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
May 8, 2023
Identification of complement factor H variants that predispose to pre-eclampsia: A genetic and functional study
A Inkeri Lokki, Zhen Ren, Michael Triebwasser, et al.
Genome Research
|
December 25, 2019
Identification of pathogenic variant enriched regions across genes and gene families
Eduardo Pérez-Palma, Patrick May, Sumaiya Iqbal, et al.
Page
of 15