Works matching IS 00015652 AND DT 2022

Results: 11

The Prevalence of JAK2 Exon 12 Mutations in Vietnamese Patients with JAK2 V617F-Negative Polycythemia Vera: Frequent or Rare?

Published in:

Human Heredity, 2022, v. 87, n. 3/4, p. 102, doi. 10.1159/000526201

By:

Ngoc, Nguyen Thy;
Linh, Nguyen Thuy;
Xuan, Nguyen Thi

Publication type:

Article

Identification of CHEK2 Germline Mutations in BRCA1/2- and PALB2-Negative Breast and Ovarian Cancer Patients.

Published in:

Human Heredity, 2022, v. 87, n. 2, p. 21, doi. 10.1159/000521369

By:

Aksoy, Fuat;
Tezcan Unlu, Havva;
Cecener, Gulsah;
Guney Eskiler, Gamze;
Egeli, Unal;
Tunca, Berrin;
Efendi Erdem, Ecem;
Senol, Kazım;
Gokgoz, Mustafa Sehsuvar

Publication type:

Article

50th European Mathematical Genetics Meeting (EMGM) 2022.

Published in:: 2022
Publication type:: Abstract

Common Variants in Neuraminidase Genes Contribute to Predisposition to and Progression of Chronic Heart Failure.

Published in:

Human Heredity, 2022, v. 87, n. 3/4, p. 96, doi. 10.1159/000525713

By:

Li, Shiyang;
Wang, Yuehong;
Zeng, Xiaobing;
Zhang, Yanyu;
Wang, Shihai;
Liu, Yuyong;
Xu, Dawen;
Lan, Jianjun;
Hu, Dong

Publication type:

Article

Mutational Screening for Mitochondrial tRNA Genes in 100 Women with Pre-Eclampsia.

Published in:

Human Heredity, 2022, v. 87, n. 3/4, p. 87, doi. 10.1159/000525663

By:

Zhou, Baohua;
Chu, Xuelian;
Zhang, Caijuan;
Liang, Xiufeng

Publication type:

Article

Penalized Logistic Regression Analysis for Genetic Association Studies of Binary Phenotypes.

Published in:

Human Heredity, 2022, v. 87, n. 3/4, p. 69, doi. 10.1159/000525650

By:

Yu, Ying;
Chen, Siyuan;
Jones, Samantha Jean;
Hoque, Rawnak;
Vishnyakova, Olga;
Brooks-Wilson, Angela;
McNeney, Brad

Publication type:

Article

Identification of a Novel Mutation in Patients with Type A Insulin Resistance Syndrome.

Published in:

Human Heredity, 2022, v. 87, n. 2, p. 60, doi. 10.1159/000525223

By:

Zhao, Liling;
Dai, Hongmei;
Zhang, Qin;
Hu, Wenmu;
Jin, Ping

Publication type:

Article

The Mitochondrial tRNA<sup>Asp</sup> T7561C, tRNA<sup>His</sup> C12153T, and A12172G Mutations May Be Associated with Essential Hypertension in a Han Chinese Pedigree.

Published in:

Human Heredity, 2022, v. 87, n. 2, p. 51, doi. 10.1159/000524163

By:

Fu, Haiying;
Sun, Jinming;
Xu, Xiaoyan

Publication type:

Article

Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts.

Published in:

Human Heredity, 2022, v. 87, n. 2, p. 34, doi. 10.1159/000522642

By:

Alotaibi, Rasha N.;
Howe, Brian J.;
Moreno Uribe, Lina M.;
Sanchez, Carla;
Deleyiannis, Frederic W.B.;
Padilla, Carmencita;
Poletta, Fernando A.;
Orioli, Ieda M.;
Buxó, Carmen J.;
Wehby, George L.;
Vieira, Alexandre R.;
Murray, Jeffrey;
Valencia-Ramírez, Consuelo;
Restrepo Muñeton, Claudia P.;
Long, Ross E.;
Shaffer, John R.;
Reis, Steven E.;
Weinberg, Seth M.;
Neiswanger, Katherine;
McNeil, Daniel W.

Publication type:

Article

Screening for Mitochondrial tRNA Mutations in 318 Patients with Dilated Cardiomyopathy.

Published in:

Human Heredity, 2022, v. 87, n. 1, p. 1, doi. 10.1159/000521615

By:

Qi, Yujuan;
Wu, Zhenhua;
Bai, Yaobang;
Jiao, Yan;
Li, Peijun

Publication type:

Article

Family History of Breast Cancer Is Associated with Elevated Risk of Prostate Cancer: Evidence for Shared Genetic Risks.

Published in:

Human Heredity, 2022, v. 87, n. 1, p. 12, doi. 10.1159/000521215

By:

Calvo Chozas, Adrián;
Mahjani, Behrang;
Rönnegård, Lars

Publication type:

Article