1-9 of 9
Authors: Peter Lichtner
Journal Article
First mitochondrial genome-wide association study with metabolomics Open Access
Human Molecular Genetics, Volume 31, Issue 19, 1 October 2022, Pages 3367–3376, https://doi.org/10.1093/hmg/ddab312
Published: 27 October 2021
Journal Article
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency Free
Human Molecular Genetics, Volume 27, Issue 4, 15 February 2018, Pages 706–715, https://doi.org/10.1093/hmg/ddx436
Published: 05 January 2018
Includes: Multimedia
Journal Article
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk Get access
Human Molecular Genetics, Volume 24, Issue 1, 1 January 2015, Pages 285–298, https://doi.org/10.1093/hmg/ddu431
Published: 28 August 2014
Journal Article
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease Get access
Human Molecular Genetics, Volume 22, Issue 5, 1 March 2013, Pages 1039–1049, https://doi.org/10.1093/hmg/dds492
Published: 07 December 2012
Journal Article
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11 Get access
Human Molecular Genetics, Volume 21, Issue 24, 15 December 2012, Pages 5373–5384, https://doi.org/10.1093/hmg/dds381
Published: 13 September 2012
Journal Article
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels Get access
Human Molecular Genetics, Volume 20, Issue 5, 1 March 2011, Pages 1042–1047, https://doi.org/10.1093/hmg/ddq538
Published: 10 December 2010
Journal Article
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations Open Access
Human Molecular Genetics, Volume 18, Issue 12, 15 June 2009, Pages 2288–2296, https://doi.org/10.1093/hmg/ddp135
Published: 20 March 2009
Journal Article
Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk Get access
Human Molecular Genetics, Volume 14, Issue 21, 1 November 2005, Pages 3227–3236, https://doi.org/10.1093/hmg/ddi353
Published: 20 September 2005
Journal Article
Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency Get access
Human Molecular Genetics, Volume 10, Issue 12, 1 June 2001, Pages 1299–1306, https://doi.org/10.1093/hmg/10.12.1299
Published: 01 June 2001
