Yang H - Search Results

1

High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization.

Zhang X, Snijders A, Segraves R, Zhang X, Niebuhr A, Albertson D, Yang H, Gray J, Niebuhr E, Bolund L, Pinkel D. Zhang X, et al. Among authors: yang h. Am J Hum Genet. 2005 Feb;76(2):312-26. doi: 10.1086/427762. Epub 2005 Jan 4. Am J Hum Genet. 2005. PMID: 15635506 Free PMC article.

2

A deletion panel of the long arm of the X chromosome: subregional localization of 22 DNA probes.

Yang HM, Lund T, Niebuhr E, Nørby S, Schwartz M, Shen L. Yang HM, et al. Hum Genet. 1990 Jun;85(1):25-30. doi: 10.1007/BF00276321. Hum Genet. 1990. PMID: 1972695

3

Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia.

Schwartz M, Yang HM, Niebuhr E, Rosenberg T, Page DC. Schwartz M, et al. Among authors: yang hm. Hum Genet. 1988 Feb;78(2):156-60. doi: 10.1007/BF00278188. Hum Genet. 1988. PMID: 3422216

4

Exclusion mapping of 12 X-linked disease loci and 10 DNA probes from the long arm of the X-chromosome.

Yang HM, Lund T, Niebuhr E, Nørby S, Schwartz M, Shen L. Yang HM, et al. Clin Genet. 1990 Aug;38(2):94-104. doi: 10.1111/j.1399-0004.1990.tb03555.x. Clin Genet. 1990. PMID: 1976460

5

Choroideremia, congenital deafness and mental retardation in a family with an X chromosomal deletion.

Rosenberg T, Niebuhr E, Yang HM, Parving A, Schwartz M. Rosenberg T, et al. Among authors: yang hm. Ophthalmic Paediatr Genet. 1987 Nov;8(3):139-43. doi: 10.3109/13816818709031459. Ophthalmic Paediatr Genet. 1987. PMID: 3438052

6

Choroideremia: further evidence for assignment of the locus to Xq13-Xq21.

Schwartz M, Rosenberg T, Niebuhr E, Lundsteen C, Sardemann H, Andersen O, Yang HM, Lamm LU. Schwartz M, et al. Among authors: yang hm. Hum Genet. 1986 Dec;74(4):449-52. doi: 10.1007/BF00280505. Hum Genet. 1986. PMID: 2878872

7

Choroideremia in interstitial deletion of the X chromosome.

Rosenberg T, Schwartz M, Niebuhr E, Yang HM, Sardemann H, Andersen O, Lundsteen C. Rosenberg T, et al. Among authors: yang hm. Ophthalmic Paediatr Genet. 1986 Dec;7(3):205-10. doi: 10.3109/13816818609004140. Ophthalmic Paediatr Genet. 1986. PMID: 2882458

8

The Association of Mitochondrial tRNA^Cys G5783A Mutation with Major Depressive Disorder in Two Han Chinese Families.

Jing P, Yu H, Sun W, Liang M, Xia T, Yang H, Chen P, Li J, Zhang X. Jing P, et al. Among authors: yang h. Neuropsychiatr Dis Treat. 2025 Jan 3;21:15-24. doi: 10.2147/NDT.S465744. eCollection 2025. Neuropsychiatr Dis Treat. 2025. PMID: 39776895 Free PMC article.

9

Exploring causal relationships between immune cells and age-related macular degeneration through univariable, bidirectional, and multivariable Mendelian analysis.

Wei X, Yang H, Yin X, Fu Z, Xiong W. Wei X, et al. Among authors: yang h. Front Med (Lausanne). 2024 Dec 24;11:1444277. doi: 10.3389/fmed.2024.1444277. eCollection 2024. Front Med (Lausanne). 2024. PMID: 39776840 Free PMC article.

10

A specific and adaptable approach to track CD206⁺ macrophages by molecular MRI and fluorescence imaging.

Wang C, Jalali Motlagh N, Wojtkiewicz GR, Yang H, Kim HH, Chen JW. Wang C, et al. Among authors: yang h. Theranostics. 2025 Jan 1;15(3):1094-1109. doi: 10.7150/thno.96488. eCollection 2025. Theranostics. 2025. PMID: 39776805 Free PMC article.

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