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
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
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

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

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

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

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

Unraveling phenotypic variance in metabolic syndrome through multi-omics.

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

Genetics and epigenetics of diabetes and its complications in India.

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