| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Biased Allelic Expression in Human Primary Fibroblast Single Cells
|
Borel, Christelle
|
|
2015
|
96 |
1 |
p. 70-80
11 p.
|
artikel
|
| 2 |
CODAS Syndrome Is Associated with Mutations of LONP1, Encoding Mitochondrial AAA+ Lon Protease
|
Strauss, Kevin A.
|
|
2015
|
96 |
1 |
p. 121-135
15 p.
|
artikel
|
| 3 |
CRB2 Mutations Produce a Phenotype Resembling Congenital Nephrosis, Finnish Type, with Cerebral Ventriculomegaly and Raised Alpha-Fetoprotein
|
Slavotinek, Anne
|
|
2015
|
96 |
1 |
p. 162-169
8 p.
|
artikel
|
| 4 |
DCDC2 Mutations Cause a Renal-Hepatic Ciliopathy by Disrupting Wnt Signaling
|
Schueler, Markus
|
|
2015
|
96 |
1 |
p. 81-92
12 p.
|
artikel
|
| 5 |
Defects of CRB2 Cause Steroid-Resistant Nephrotic Syndrome
|
Ebarasi, Lwaki
|
|
2015
|
96 |
1 |
p. 153-161
9 p.
|
artikel
|
| 6 |
Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1
|
Glubb, Dylan M.
|
|
2015
|
96 |
1 |
p. 5-20
16 p.
|
artikel
|
| 7 |
Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms
|
Baurecht, Hansjörg
|
|
2015
|
96 |
1 |
p. 104-120
17 p.
|
artikel
|
| 8 |
HLA-DPB1 and HLA Class I Confer Risk of and Protection from Narcolepsy
|
Ollila, Hanna M.
|
|
2015
|
96 |
1 |
p. 136-146
11 p.
|
artikel
|
| 9 |
Improvement of SMN2 Pre-mRNA Processing Mediated by Exon-Specific U1 Small Nuclear RNA
|
Dal Mas, Andrea
|
|
2015
|
96 |
1 |
p. 93-103
11 p.
|
artikel
|
| 10 |
MAT2A Mutations Predispose Individuals to Thoracic Aortic Aneurysms
|
Guo, Dong-chuan
|
|
2015
|
96 |
1 |
p. 170-177
8 p.
|
artikel
|
| 11 |
Meta-analysis of Correlated Traits via Summary Statistics from GWASs with an Application in Hypertension
|
Zhu, Xiaofeng
|
|
2015
|
96 |
1 |
p. 21-36
16 p.
|
artikel
|
| 12 |
Mutations Affecting the SAND Domain of DEAF1 Cause Intellectual Disability with Severe Speech Impairment and Behavioral Problems
|
Vulto-van Silfhout, Anneke T.
|
|
2015
|
96 |
1 |
p. 178-
1 p.
|
artikel
|
| 13 |
Recessive Mutations in COL25A1 Are a Cause of Congenital Cranial Dysinnervation Disorder
|
Shinwari, Jameela M.A.
|
|
2015
|
96 |
1 |
p. 147-152
6 p.
|
artikel
|
| 14 |
The Genetic Ancestry of African Americans, Latinos, and European Americans across the United States
|
Bryc, Katarzyna
|
|
2015
|
96 |
1 |
p. 37-53
17 p.
|
artikel
|
| 15 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2015
|
96 |
1 |
p. 3-4
2 p.
|
artikel
|
| 16 |
This Month in The Journal
|
Ratzel, Sarah
|
|
2015
|
96 |
1 |
p. 1-2
2 p.
|
artikel
|
| 17 |
Uncovering the Genetic History of the Present-Day Greenlandic Population
|
Moltke, Ida
|
|
2015
|
96 |
1 |
p. 54-69
16 p.
|
artikel
|
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