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 |