Volume 99; Issue 5

The American Journal of Human Genetics

Volume 99; Issue 5

1

Evolution of Cell-to-Cell Variability in Stochastic, Controlled, Heteroplasmic mtDNA Populations

Johnston, Iain G., Jones, Nick S.

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.86 MB

english, 2016

2

Recessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis Imperfecta

Seymen, Figen, Kim, Youn Jung, Lee, Ye Ji, Kang, Jenny, Kim, Tak-Heun, Choi, Hwajung, Koruyucu, Mine, Kasimoglu, Yelda, Tuna, Elif Bahar, Gencay, Koray, Shin, Teo Jeon, Hyun, Hong-Keun, Kim, Young-Jae

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 2.72 MB

english, 2016

3

Was ADH1B under Selection in European Populations?

Shen, Quan-Kuan, Sulaiman, Xierzhatijiang, Yao, Yong-Gang, Peng, Min-Sheng, Zhang, Ya-Ping

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 648 KB

english, 2016

4

Response to Shen et al.

Galinsky, Kevin J., Bhatia, Gaurav, Loh, Po-Ru, Georgiev, Stoyan, Mukherjee, Sayan, Patterson, Nick J., Price, Alkes L.

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 325 KB

english, 2016

5

Allele-Specific Methylome and Transcriptome Analysis Reveals Widespread Imprinting in the Human Placenta

Hamada, Hirotaka, Okae, Hiroaki, Toh, Hidehiro, Chiba, Hatsune, Hiura, Hitoshi, Shirane, Kenjiro, Sato, Tetsuya, Suyama, Mikita, Yaegashi, Nobuo, Sasaki, Hiroyuki, Arima, Takahiro

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 2.71 MB

english, 2016

6

Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss

Namburi, Prasanthi, Ratnapriya, Rinki, Khateb, Samer, Lazar, Csilla H., Kinarty, Yael, Obolensky, Alexey, Erdinest, Inbar, Marks-Ohana, Devorah, Pras, Eran, Ben-Yosef, Tamar, Newman, Hadas, Gross, Men

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 62 KB

english, 2016

7

This Month in Genetics

Garber, Kathryn B.

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 45 KB

english, 2016

8

GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism

Guan, Bin, Welch, James M., Sapp, Julie C., Ling, Hua, Li, Yulong, Johnston, Jennifer J., Kebebew, Electron, Biesecker, Leslie G., Simonds, William F., Marx, Stephen J., Agarwal, Sunita K.

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 900 KB

english, 2016

9

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S , which Encode Subcomponents C1r and C1s of Complement

Kapferer-Seebacher, Ines, Pepin, Melanie, Werner, Roland, Aitman, Timothy J., Nordgren, Ann, Stoiber, Heribert, Thielens, Nicole, Gaboriaud, Christine, Amberger, Albert, Schossig, Anna, Gruber, Robert

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.67 MB

english, 2016

10

This Month in The Journal

Ratzel, Sarah, Cullinan, Sara B.

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 44 KB

english, 2016

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