no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome
|
Borck, Guntram |
|
2010 |
129 |
1 |
p. 45-50 |
article |
2 |
A novel survival multifactor dimensionality reduction method for detecting gene–gene interactions with application to bladder cancer prognosis
|
Gui, Jiang |
|
2010 |
129 |
1 |
p. 101-110 |
article |
3 |
−13915*G DNA polymorphism associated with lactase persistence in Africa interacts with Oct-1
|
Olds, Lynne C. |
|
2010 |
129 |
1 |
p. 111-113 |
article |
4 |
Genetic variants in the KIF6 region and coronary event reduction from statin therapy
|
Li, Yonghong |
|
2010 |
129 |
1 |
p. 17-23 |
article |
5 |
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16
|
Chapman, Nicola H. |
|
2010 |
129 |
1 |
p. 59-70 |
article |
6 |
Genome-wide analysis of copy number variants in age-related macular degeneration
|
Meyer, Kacie J. |
|
2010 |
129 |
1 |
p. 91-100 |
article |
7 |
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21
|
Piret, Sian E. |
|
2010 |
129 |
1 |
p. 51-58 |
article |
8 |
Heather Skirton and Christine Patch: Genetics for the health sciences: a handbook for clinical healthcare
|
Thistlewood, Helen |
|
2010 |
129 |
1 |
p. 115 |
article |
9 |
Mechanisms for phenotypic variation in Lesch–Nyhan disease and its variants
|
Sampat, Radhika |
|
2010 |
129 |
1 |
p. 71-78 |
article |
10 |
Mutation analysis in Bardet–Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals
|
Janssen, Sabine |
|
2010 |
129 |
1 |
p. 79-90 |
article |
11 |
Partial correlation network analyses to detect altered gene interactions in human disease: using preeclampsia as a model
|
Johansson, Åsa |
|
2010 |
129 |
1 |
p. 25-34 |
article |
12 |
Regions of homozygosity and their impact on complex diseases and traits
|
Ku, Chee Seng |
|
2010 |
129 |
1 |
p. 1-15 |
article |
13 |
Sperm rates of 7q11.23, 15q11q13 and 22q11.2 deletions and duplications: a FISH approach
|
Molina, Oscar |
|
2010 |
129 |
1 |
p. 35-44 |
article |