Works matching IS 03406717 AND DT 2024 AND VI 143 AND IP 1

Results: 7

Recombination map tailored to Native Hawaiians may improve robustness of genomic scans for positive selection.

Published in:

Human Genetics, 2024, v. 143, n. 1, p. 85, doi. 10.1007/s00439-023-02625-2

By:

Dinh, Bryan L.;
Tang, Echo;
Taparra, Kekoa;
Nakatsuka, Nathan;
Chen, Fei;
Chiang, Charleston W. K.

Publication type:

Article

Delineation of the adult phenotype of Coffin–Siris syndrome in 35 individuals.

Published in:

Human Genetics, 2024, v. 143, n. 1, p. 71, doi. 10.1007/s00439-023-02622-5

By:

Schmetz, Ariane;
Lüdecke, Hermann-Josef;
Surowy, Harald;
Sivalingam, Sugirtahn;
Bruel, Ange-Line;
Caumes, Roseline;
Charles, Perrine;
Chatron, Nicolas;
Chrzanowska, Krystyna;
Codina-Solà, Marta;
Colson, Cindy;
Cuscó, Ivon;
Denommé-Pichon, Anne-Sophie;
Edery, Patrick;
Faivre, Laurence;
Green, Andrew;
Heide, Solveig;
Hsieh, Tzung-Chien;
Hustinx, Alexander;
Kleinendorst, Lotte

Publication type:

Article

Genomic analysis of presumed perinatal stroke in Saudi Arabia reveals a strong monogenic contribution.

Published in:

Human Genetics, 2024, v. 143, n. 1, p. 59, doi. 10.1007/s00439-023-02621-6

By:

Alshammari, Muneera J.;
Shamseldin, Hanan E.;
Essbaiheen, Fahad;
Eltahir, Sara H.;
Alruwaili, Ashwag R.;
Abdulwahab, Firdous;
Alkuraya, Fowzan S.

Publication type:

Article

Unraveling phenotypic variance in metabolic syndrome through multi-omics.

Published in:

Human Genetics, 2024, v. 143, n. 1, p. 35, doi. 10.1007/s00439-023-02619-0

By:

Amente, Lamessa Dube;
Mills, Natalie T;
Le, Thuc Duy;
Hyppönen, Elina;
Lee, S. Hong

Publication type:

Article

rs10924104 in the expression enhancer motif of CD58 confers susceptibility to human autoimmune diseases.

Published in:

Human Genetics, 2024, v. 143, n. 1, p. 19, doi. 10.1007/s00439-023-02617-2

By:

Hitomi, Yuki;
Ueno, Kazuko;
Aiba, Yoshihiro;
Nishida, Nao;
Kawai, Yosuke;
Kawashima, Minae;
Khor, Seik-Soon;
Takada, Sanami;
Iwabuchi, Chisato;
Nagasaki, Masao;
Tokunaga, Katsushi;
Nakamura, Minoru

Publication type:

Article

Genome-wide association and Mendelian randomization analysis provide insights into the shared genetic architecture between high-dimensional electrocardiographic features and ischemic heart disease.

Published in:

Human Genetics, 2024, v. 143, n. 1, p. 49, doi. 10.1007/s00439-023-02614-5

By:

Wang, Xinfeng;
Qi, Mengling;
Zhang, Haoyang;
Yang, Yuedong;
Zhao, Huiying

Publication type:

Article

Genetics and epigenetics of diabetes and its complications in India.

Published in:

Human Genetics, 2024, v. 143, n. 1, p. 1, doi. 10.1007/s00439-023-02616-3

By:

Priyadarshini, Ankita;
Madan, Riya;
Das, Sadhan

Publication type:

Article