Works matching IS 03406717 AND DT 2021 AND VI 140 AND IP 2

Results: 10

Deciphering the complexity of simple chromosomal insertions by genome sequencing.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 361, doi. 10.1007/s00439-020-02210-x

By:

Dong, Zirui;
Chau, Matthew Hoi Kin;
Zhang, Yanyan;
Dai, Peng;
Zhu, Xiaofan;
Leung, Tak Yeung;
Kong, Xiangdong;
Kwok, Yvonne K.;
Stankiewicz, Paweł;
Cheung, Sau Wai;
Choy, Kwong Wai

Publication type:

Article

Genetic evidence suggests a sense of family, parity and conquest in the Xiongnu Iron Age nomads of Mongolia.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 349, doi. 10.1007/s00439-020-02209-4

By:

Keyser, Christine;
Zvénigorosky, Vincent;
Gonzalez, Angéla;
Fausser, Jean-Luc;
Jagorel, Florence;
Gérard, Patrice;
Tsagaan, Turbat;
Duchesne, Sylvie;
Crubézy, Eric;
Ludes, Bertrand

Publication type:

Article

Population genetics: past, present, and future.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 231, doi. 10.1007/s00439-020-02208-5

By:

Okazaki, Atsuko;
Yamazaki, Satoru;
Inoue, Ituro;
Ott, Jurg

Publication type:

Article

Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 321, doi. 10.1007/s00439-020-02207-6

By:

Horiuchi, Yasue;
Matsubayashi, Hiroyuki;
Kiyozumi, Yoshimi;
Nishimura, Seiichiro;
Higashigawa, Satomi;
Kado, Nobuhiro;
Nagashima, Takeshi;
Mizuguchi, Maki;
Ohnami, Sumiko;
Arai, Makoto;
Urakami, Kenichi;
Kusuhara, Masatoshi;
Yamaguchi, Ken

Publication type:

Article

Identifying adaptive alleles in the human genome: from selection mapping to functional validation.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 241, doi. 10.1007/s00439-020-02206-7

By:

Werren, Elizabeth A.;
Garcia, Obed;
Bigham, Abigail W.

Publication type:

Article

A pooled genome-wide association study identifies pancreatic cancer susceptibility loci on chromosome 19p12 and 19p13.3 in the full-Jewish population.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 309, doi. 10.1007/s00439-020-02205-8

By:

Streicher, Samantha A.;
Klein, Alison P.;
Olson, Sara H.;
Kurtz, Robert C.;
Amundadottir, Laufey T.;
DeWan, Andrew T.;
Zhao, Hongyu;
Risch, Harvey A.

Publication type:

Article

A Southeast Asian origin for present-day non-African human Y chromosomes.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 299, doi. 10.1007/s00439-020-02204-9

By:

Hallast, Pille;
Agdzhoyan, Anastasia;
Balanovsky, Oleg;
Xue, Yali;
Tyler-Smith, Chris

Publication type:

Article

Interplay between probe design and test performance: overlap between genomic regions of interest, capture regions and high quality reference calls influence performance of WES-based assays.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 289, doi. 10.1007/s00439-020-02201-y

By:

Pranckeviciene, Erinija;
Racacho, Lemuel;
Ghani, Mahdi;
Nfonsam, Landry;
Potter, Ryan;
Sinclair-Bourque, Elizabeth;
Mettler, Gabrielle;
Smith, Amanda;
Bronicki, Lucas;
Huang, Lijia;
Jarinova, Olga

Publication type:

Article

Combi-CRISPR: combination of NHEJ and HDR provides efficient and precise plasmid-based knock-ins in mice and rats.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 277, doi. 10.1007/s00439-020-02198-4

By:

Yoshimi, Kazuto;
Oka, Yuichiro;
Miyasaka, Yoshiki;
Kotani, Yuko;
Yasumura, Misato;
Uno, Yoshihiro;
Hattori, Kosuke;
Tanigawa, Arisa;
Sato, Makoto;
Oya, Manami;
Nakamura, Kazuhiro;
Matsushita, Natsuki;
Kobayashi, Kazuto;
Mashimo, Tomoji

Publication type:

Article

Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease.

Published in:

Human Genetics, 2021, v. 140, n. 2, p. 333, doi. 10.1007/s00439-020-02200-z

By:

Fu, Fang;
Li, Ru;
Lei, Ting-ying;
Wang, Dan;
Yang, Xin;
Han, Jin;
Pan, Min;
Zhen, Li;
Li, Jian;
Li, Fa-tao;
Jing, Xiang-yi;
Li, Dong-zhi;
Liao, Can

Publication type:

Article