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European Journal of Human Genetics : EJHG
|
September 11, 2008
Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study)
Linda T Roten, Matthew P Johnson, Siri Forsmo, et al.
Human Genetics
|
October 9, 2010
Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model
Asa Johansson, Mari Løset, Siv B Mundal, et al.
Human Genetics
|
July 7, 2009
The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations
Matthew P Johnson, Linda T Roten, Thomas D Dyer, et al.
Bioinformatics (Oxford, England)
|
December 23, 2016
The Ark: a customizable web-based data management tool for health and medical research
Adrian Bickerstaffe, Thilina Ranaweera, Travis Endersby, et al.
BMC Medical Genetics
|
May 5, 2019
Identification of novel sarcoma risk genes using a two-stage genome wide DNA sequencing strategy in cancer cluster families and population case and control cohorts
Rachel M Jones, Phillip E Melton, Mark Pinese, et al.
Atherosclerosis
|
December 4, 2021
Cascade testing for elevated lipoprotein(a) in relatives of probands with familial hypercholesterolaemia and elevated lipoprotein(a)
Anindita Chakraborty, Jing Pang, Dick C Chan, et al.
American Journal of Preventive Cardiology
|
May 6, 2022
Cascade testing for elevated lipoprotein(a) in relatives of probands with high lipoprotein(a)
Anindita Chakraborty, Dick C Chan, Katrina L Ellis, et al.
Scientific Reports
|
July 26, 2017
Environment Changes Genetic Effects on Respiratory Conditions and Allergic Phenotypes
Yong Song, Michelle J Schwager, Vibeke Backer, et al.
Journal of Medical Genetics
|
May 7, 2011
The 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cells
Katy A Freed, John Blangero, Tom Howard, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
January 10, 2009
The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population
Joanne M Said, Shaun P Brennecke, Eric K Moses, et al.
Page
of 12
Search research articles
Search
Showing results (31-40 of 112) with videos related to
Sort By:
Page
of 12
European Journal of Human Genetics : EJHG
|
September 11, 2008
Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study)
Linda T Roten, Matthew P Johnson, Siri Forsmo, et al.
Human Genetics
|
October 9, 2010
Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model
Asa Johansson, Mari Løset, Siv B Mundal, et al.
Human Genetics
|
July 7, 2009
The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations
Matthew P Johnson, Linda T Roten, Thomas D Dyer, et al.
Bioinformatics (Oxford, England)
|
December 23, 2016
The Ark: a customizable web-based data management tool for health and medical research
Adrian Bickerstaffe, Thilina Ranaweera, Travis Endersby, et al.
BMC Medical Genetics
|
May 5, 2019
Identification of novel sarcoma risk genes using a two-stage genome wide DNA sequencing strategy in cancer cluster families and population case and control cohorts
Rachel M Jones, Phillip E Melton, Mark Pinese, et al.
Atherosclerosis
|
December 4, 2021
Cascade testing for elevated lipoprotein(a) in relatives of probands with familial hypercholesterolaemia and elevated lipoprotein(a)
Anindita Chakraborty, Jing Pang, Dick C Chan, et al.
American Journal of Preventive Cardiology
|
May 6, 2022
Cascade testing for elevated lipoprotein(a) in relatives of probands with high lipoprotein(a)
Anindita Chakraborty, Dick C Chan, Katrina L Ellis, et al.
Scientific Reports
|
July 26, 2017
Environment Changes Genetic Effects on Respiratory Conditions and Allergic Phenotypes
Yong Song, Michelle J Schwager, Vibeke Backer, et al.
Journal of Medical Genetics
|
May 7, 2011
The 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cells
Katy A Freed, John Blangero, Tom Howard, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|
January 10, 2009
The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population
Joanne M Said, Shaun P Brennecke, Eric K Moses, et al.
Page
of 12