| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abraham's Children in the Genome Era: Major Jewish Diaspora Populations Comprise Distinct Genetic Clusters with Shared Middle Eastern Ancestry
|
Atzmon, Gil
|
|
2010
|
86 |
6 |
p. 850-859
10 p.
|
artikel
|
| 2 |
A Definitive Haplotype Map as Determined by Genotyping Duplicated Haploid Genomes Finds a Predominant Haplotype Preference at Copy-Number Variation Events
|
Kukita, Yoji
|
|
2010
|
86 |
6 |
p. 918-928
11 p.
|
artikel
|
| 3 |
Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene
|
Walczak-Sztulpa, Joanna
|
|
2010
|
86 |
6 |
p. 949-956
8 p.
|
artikel
|
| 4 |
Dominant-Negative Mutations in α-II Spectrin Cause West Syndrome with Severe Cerebral Hypomyelination, Spastic Quadriplegia, and Developmental Delay
|
Saitsu, Hirotomo
|
|
2010
|
86 |
6 |
p. 881-891
11 p.
|
artikel
|
| 5 |
Evolutionary and Functional Analysis of Celiac Risk Loci Reveals SH2B3 as a Protective Factor against Bacterial Infection
|
Zhernakova, Alexandra
|
|
2010
|
86 |
6 |
p. 970-977
8 p.
|
artikel
|
| 6 |
Female-to-Male Breeding Ratio in Modern Humans—an Analysis Based on Historical Recombinations
|
Labuda, Damian
|
|
2010
|
86 |
6 |
p. 982-
1 p.
|
artikel
|
| 7 |
GJC2 Missense Mutations Cause Human Lymphedema
|
Ferrell, Robert E.
|
|
2010
|
86 |
6 |
p. 943-948
6 p.
|
artikel
|
| 8 |
Haploinsufficiency of TAB2 Causes Congenital Heart Defects in Humans
|
Thienpont, Bernard
|
|
2010
|
86 |
6 |
p. 839-849
11 p.
|
artikel
|
| 9 |
Identification of a Kir3.4 Mutation in Congenital Long QT Syndrome
|
Yang, Yanzong
|
|
2010
|
86 |
6 |
p. 872-880
9 p.
|
artikel
|
| 10 |
Insights into Colon Cancer Etiology via a Regularized Approach to Gene Set Analysis of GWAS Data
|
Chen, Lin S.
|
|
2010
|
86 |
6 |
p. 860-871
12 p.
|
artikel
|
| 11 |
Loss-of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome
|
Pang, Junfeng
|
|
2010
|
86 |
6 |
p. 957-962
6 p.
|
artikel
|
| 12 |
Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability
|
Zhang, Feng
|
|
2010
|
86 |
6 |
p. 892-903
12 p.
|
artikel
|
| 13 |
Mutations in HPSE2 Cause Urofacial Syndrome
|
Daly, Sarah B.
|
|
2010
|
86 |
6 |
p. 963-969
7 p.
|
artikel
|
| 14 |
Pooled Association Tests for Rare Variants in Exon-Resequencing Studies
|
Price, Alkes L.
|
|
2010
|
86 |
6 |
p. 982-
1 p.
|
artikel
|
| 15 |
Pooled Association Tests for Rare Variants in Exon-Resequencing Studies
|
Price, Alkes L.
|
|
2010
|
86 |
6 |
p. 832-838
7 p.
|
artikel
|
| 16 |
Powerful SNP-Set Analysis for Case-Control Genome-wide Association Studies
|
Wu, Michael C.
|
|
2010
|
86 |
6 |
p. 929-942
14 p.
|
artikel
|
| 17 |
Principal-Component Analysis for Assessment of Population Stratification in Mitochondrial Medical Genetics
|
Biffi, Alessandro
|
|
2010
|
86 |
6 |
p. 904-917
14 p.
|
artikel
|
| 18 |
Response to Lohmueller et al.
|
Labuda, Damian
|
|
2010
|
86 |
6 |
p. 980-981
2 p.
|
artikel
|
| 19 |
Sex-Averaged Recombination and Mutation Rates on the X Chromosome: A Comment on Labuda et al.
|
Lohmueller, Kirk E.
|
|
2010
|
86 |
6 |
p. 978-980
3 p.
|
artikel
|
| 20 |
The Woman Who Walked into the Sea: Huntington's and the Making of a Genetic Disease
|
Uhlmann, Wendy R.
|
|
2010
|
86 |
6 |
p. 830-831
2 p.
|
artikel
|
| 21 |
This Month in Genetics
|
Garber, Kathryn B.
|
|
2010
|
86 |
6 |
p. 827-829
3 p.
|
artikel
|
| 22 |
This Month in The Journal
|
Bungartz, Kathryn D.
|
|
2010
|
86 |
6 |
p. 825-826
2 p.
|
artikel
|
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