Cram DS - Search Results

1

Long-Molecule Sequencing: A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and β-Thalassemia Carriers.

Xu L, Mao A, Liu H, Gui B, Choy KW, Huang H, Yu Q, Zhang X, Chen M, Lin N, Chen L, Han J, Wang Y, Zhang M, Li X, He D, Lin Y, Zhang J, Cram DS, Cao H. Xu L, et al. Among authors: cram ds. J Mol Diagn. 2020 Aug;22(8):1087-1095. doi: 10.1016/j.jmoldx.2020.05.004. Epub 2020 May 29. J Mol Diagn. 2020. PMID: 32473995 Free article.

2

A More Universal Approach to Comprehensive Analysis of Thalassemia Alleles (CATSA).

Liang Q, Gu W, Chen P, Li Y, Liu Y, Tian M, Zhou Q, Qi H, Zhang Y, He J, Li Q, Tang L, Tang J, Teng Y, Zhou Y, Huang S, Lu Z, Xu M, Hou W, Huang T, Li Y, Li R, Hu L, Li S, Guo Q, Zhuo Z, Mou Y, Cram DS, Wu L. Liang Q, et al. Among authors: cram ds. J Mol Diagn. 2021 Sep;23(9):1195-1204. doi: 10.1016/j.jmoldx.2021.06.008. Epub 2021 Jul 20. J Mol Diagn. 2021. PMID: 34293487 Free article.

3

Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes.

Liang D, Peng Y, Lv W, Deng L, Zhang Y, Li H, Yang P, Zhang J, Song Z, Xu G, Cram DS, Wu L. Liang D, et al. Among authors: cram ds. J Mol Diagn. 2014 Sep;16(5):519-526. doi: 10.1016/j.jmoldx.2014.05.002. Epub 2014 Jul 3. J Mol Diagn. 2014. PMID: 24998187 Free article.

4

Analysis of balanced reciprocal translocations in patients with subfertility using single-molecule optical mapping.

Wang H, Jia Z, Mao A, Xu B, Wang S, Wang L, Liu S, Zhang H, Zhang X, Yu T, Mu T, Xu M, Cram DS, Yao Y. Wang H, et al. Among authors: cram ds. J Assist Reprod Genet. 2020 Mar;37(3):509-516. doi: 10.1007/s10815-020-01702-z. Epub 2020 Feb 5. J Assist Reprod Genet. 2020. PMID: 32026199 Free PMC article.

5

Single-Molecule Sequencing: A New Approach for Preimplantation Testing and Noninvasive Prenatal Diagnosis Confirmation of Fetal Genotype.

Rechitsky S, Kuliev A, San Ramon G, Tur-Kaspa I, Wang Y, Wang W, Wu X, Wang L, Leigh D, Cram DS. Rechitsky S, et al. Among authors: cram ds. J Mol Diagn. 2020 Feb;22(2):220-227. doi: 10.1016/j.jmoldx.2019.10.001. Epub 2019 Nov 18. J Mol Diagn. 2020. PMID: 31751677 Free article.

6

Maternal X chromosome copy number variations are associated with discordant fetal sex chromosome aneuploidies detected by noninvasive prenatal testing.

Wang S, Huang S, Ma L, Liang L, Zhang J, Zhang J, Cram DS. Wang S, et al. Among authors: cram ds. Clin Chim Acta. 2015 Apr 15;444:113-6. doi: 10.1016/j.cca.2015.02.014. Epub 2015 Feb 14. Clin Chim Acta. 2015. PMID: 25689220

7

The Performance of Whole Genome Amplification Methods and Next-Generation Sequencing for Pre-Implantation Genetic Diagnosis of Chromosomal Abnormalities.

Li N, Wang L, Wang H, Ma M, Wang X, Li Y, Zhang W, Zhang J, Cram DS, Yao Y. Li N, et al. Among authors: cram ds. J Genet Genomics. 2015 Apr 20;42(4):151-9. doi: 10.1016/j.jgg.2015.03.001. Epub 2015 Mar 14. J Genet Genomics. 2015. PMID: 25953353

8

The clinical utility of next-generation sequencing for identifying chromosome disease syndromes in human embryos.

Fan J, Wang L, Wang H, Ma M, Wang S, Liu Z, Xu G, Zhang J, Cram DS, Yao Y. Fan J, et al. Among authors: cram ds. Reprod Biomed Online. 2015 Jul;31(1):62-70. doi: 10.1016/j.rbmo.2015.03.010. Epub 2015 Apr 9. Reprod Biomed Online. 2015. PMID: 25985995

9

Variant haplophasing by long-read sequencing: a new approach to preimplantation genetic testing workups.

M M YC, Yu Q, Ma M, Wang H, Tian S, Zhang W, M M JZ, Liu Y, Yang Q, Pan X, Liang H, Wang L, Leigh D, Cram DS, Yao Y. M M YC, et al. Among authors: cram ds. Fertil Steril. 2021 Sep;116(3):774-783. doi: 10.1016/j.fertnstert.2021.04.012. Epub 2021 May 19. Fertil Steril. 2021. PMID: 34020778 Free article.

10

A PGD pregnancy achieved by embryo copy number variation sequencing with confirmation by non-invasive prenatal diagnosis.

Wang H, Wang L, Ma M, Song Z, Zhang J, Xu G, Fan J, Li N, Cram DS, Yao Y. Wang H, et al. Among authors: cram ds. J Genet Genomics. 2014 Aug 20;41(8):453-6. doi: 10.1016/j.jgg.2014.06.007. Epub 2014 Jul 17. J Genet Genomics. 2014. PMID: 25160978 No abstract available.

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