Volume 131; Issue 12

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Human Genetics
Volume 131; Issue 12

Human Genetics

Volume 131; Issue 12

1

Complement component 4 copy number variation andCYP21A2genotype associations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Chen, Wuyan, Xu, Zhi, Nishitani, Miki, Ryzin, Carol, McDonnell, Nazli B., Merke, Deborah P.

Journal:

Year:

2012

Language:

english

File:

PDF, 280 KB

english, 2012

2

Genome-wide association study of glioma and meta-analysis

Rajaraman, Preetha, Melin, Beatrice S., Wang, Zhaoming, McKean-Cowdin, Roberta, Michaud, Dominique S., Wang, Sophia S., Bondy, Melissa, Houlston, Richard, Jenkins, Robert B., Wrensch, Margaret, Yeager

Journal:

Year:

2012

Language:

english

File:

PDF, 299 KB

english, 2012

3

Two-stage association study in Chinese Han identifies two independent associations inCCR1/CCR3locus as candidate for Behçet’s disease susceptibility

Hou, Shengping, Xiao, Xiang, Li, Fuzhen, Jiang, Zhengxuan, Kijlstra, Aize, Yang, Peizeng

Journal:

Year:

2012

Language:

english

File:

PDF, 577 KB

english, 2012

4

Influences of FTO gene on onset age of adult overweight

Mei, Hao, Chen, Wei, Mills, Katherine, He, Jiang, Srinivasan, Sathanur R., Schork, Nicholas, Murray, Sarah, Berenson, Gerald S.

Journal:

Year:

2012

Language:

english

File:

PDF, 426 KB

english, 2012

5

Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset

Ramos, Eliana Marisa, Latourelle, Jeanne C., Lee, Ji-Hyun, Gillis, Tammy, Mysore, Jayalakshmi S., Squitieri, Ferdinando, Pardo, Alba, Donato, Stefano, Hayden, Michael R., Morrison, Patrick J., Nance,

Journal:

Year:

2012

Language:

english

File:

PDF, 337 KB

english, 2012

6

Network medicine: linking disorders

Piro, Rosario M.

Journal:

Year:

2012

Language:

english

File:

PDF, 172 KB

english, 2012

7

Linkage analysis for plasma amyloid beta levels in persons with hypertension implicates Aβ-40 levels to presenilin 2

Ibrahim-Verbaas, Carla A., Zorkoltseva, Irina V., Amin, Najaf, Schuur, Maaike, Coppus, Antonia M. W., Isaacs, Aaron, Aulchenko, Yurii S., Breteler, Monique M. B., Ikram, M. Arfan, Axenovich, Tatiana I

Journal:

Year:

2012

Language:

english

File:

PDF, 384 KB

english, 2012

8

Cathepsin B SNPs elevate the pathological development of oral cancer and raise the susceptibility to carcinogen-mediated oral cancer

Chen, Mu-Kuan, Su, Shih-Chi, Lin, Chiao-Wen, Tsai, Chiung-Man, Yang, Shun-Fa, Weng, Chia-Jui

Journal:

Year:

2012

Language:

english

File:

PDF, 215 KB

english, 2012

9

Genetics of familial forms of thrombocytopenia

Balduini, Carlo L., Savoia, Anna

Journal:

Year:

2012

Language:

english

File:

PDF, 263 KB

english, 2012

10

Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage–fusion–bridge for telomere stabilization

Yatsenko, Svetlana A., Hixson, Patricia, Roney, Erin K., Scott, Daryl A., Schaaf, Christian P., Ng, Yu-tze, Palmer, Robbin, Fisher, Richard B., Patel, Ankita, Cheung, Sau Wai, Lupski, James R.

Journal:

Year:

2012

Language:

english

File:

PDF, 845 KB

english, 2012

11

Pleiotropy and allelic heterogeneity in theTOMM40-APOEgenomic region related to clinical and metabolic features of hepatitis C infection

Chiba-Falek, Ornit, Linnertz, Colton, Guyton, John, Gardner, Stephen D., Roses, Allen D., McCarthy, Jeanette J., Patel, Keyur

Journal:

Year:

2012

Language:

english

File:

PDF, 302 KB

english, 2012

12

David Goldman: Our genes, our choices

Florio, Arianna

Journal:

Year:

2012

Language:

english

File:

PDF, 77 KB

english, 2012