| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Aicardi-Goutières Syndrome Is Caused by IFIH1 Mutations
|
Oda, Hirotsugu
|
|
2014
|
95 |
1 |
p. 121-125
5 p.
|
artikel
|
| 2 |
Attitudes of Genetics Professionals Toward the Return of Incidental Results from Exome and Whole-Genome Sequencing
|
Yu, Joon-Ho
|
|
2014
|
95 |
1 |
p. 77-84
8 p.
|
artikel
|
| 3 |
Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations
|
Ganesh, Santhi K.
|
|
2014
|
95 |
1 |
p. 49-65
17 p.
|
artikel
|
| 4 |
Examining Variation in Recombination Levels in the Human Female: A Test of the Production-Line Hypothesis
|
Rowsey, Ross
|
|
2014
|
95 |
1 |
p. 108-112
5 p.
|
artikel
|
| 5 |
Gene-Age Interactions in Blood Pressure Regulation: A Large-Scale Investigation with the CHARGE, Global BPgen, and ICBP Consortia
|
Simino, Jeannette
|
|
2014
|
95 |
1 |
p. 24-38
15 p.
|
artikel
|
| 6 |
Genome-wide Identification and Characterization of Fixed Human-Specific Regulatory Regions
|
Marnetto, Davide
|
|
2014
|
95 |
1 |
p. 39-48
10 p.
|
artikel
|
| 7 |
Integrative DNA, RNA, and Protein Evidence Connects TREML4 to Coronary Artery Calcification
|
Sen, Shurjo K.
|
|
2014
|
95 |
1 |
p. 66-76
11 p.
|
artikel
|
| 8 |
Joint Analysis of Functional Genomic Data and Genome-wide Association Studies of 18 Human Traits
|
Pickrell, Joseph K.
|
|
2014
|
95 |
1 |
p. 126-
1 p.
|
artikel
|
| 9 |
Mutations in SLC13A5 Cause Autosomal-Recessive Epileptic Encephalopathy with Seizure Onset in the First Days of Life
|
Thevenon, Julien
|
|
2014
|
95 |
1 |
p. 113-120
8 p.
|
artikel
|
| 10 |
PGM3 Mutations Cause a Congenital Disorder of Glycosylation with Severe Immunodeficiency and Skeletal Dysplasia
|
Stray-Pedersen, Asbjørg
|
|
2014
|
95 |
1 |
p. 96-107
12 p.
|
artikel
|
| 11 |
Rare-Variant Association Analysis: Study Designs and Statistical Tests
|
Lee, Seunggeung
|
|
2014
|
95 |
1 |
p. 5-23
19 p.
|
artikel
|
| 12 |
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
|
Al Turki, Saeed
|
|
2014
|
95 |
1 |
p. 126-
1 p.
|
artikel
|
| 13 |
Targeted Resequencing and Systematic In Vivo Functional Testing Identifies Rare Variants in MEIS1 as Significant Contributors to Restless Legs Syndrome
|
Schulte, Eva C.
|
|
2014
|
95 |
1 |
p. 85-95
11 p.
|
artikel
|
| 14 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2014
|
95 |
1 |
p. 3-4
2 p.
|
artikel
|
| 15 |
This Month in The Journal
|
Ratzel, Sarah
|
|
2014
|
95 |
1 |
p. 1-2
2 p.
|
artikel
|
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