Darmanian A[Author] - Search Results

Year	Number of Results
1999	1
2000	1
2001	2
2003	2
2004	1
2007	2
2008	1
2009	1
2010	2
2012	1
2013	1
2016	1
2021	1
2023	2
2024	0

1

Saliva DNA: An alternative biospecimen for single nucleotide polymorphism chromosomal microarray analysis in autism.

Wright DC, Baluyot ML, Carmichael J, Darmanian A, Jose N, Ngo C, Heaps LS, Yendle A, Holman K, Ziso S, Khan F, Masi A, Silove N, Eapen V. Wright DC, et al. Among authors: darmanian a. Am J Med Genet A. 2023 Dec;191(12):2913-2920. doi: 10.1002/ajmg.a.63400. Epub 2023 Sep 15. Am J Med Genet A. 2023. PMID: 37715344

2

Issues arising from the prenatal diagnosis of some rare trisomy mosaics--the importance of cryptic fetal mosaicism.

Daniel A, Wu Z, Darmanian A, Malafiej P, Tembe V, Peters G, Kennedy C, Adès L. Daniel A, et al. Among authors: darmanian a. Prenat Diagn. 2004 Jul;24(7):524-36. doi: 10.1002/pd.936. Prenat Diagn. 2004. PMID: 15300743 Review.

3

SNP chromosome microarray genotyping for detection of uniparental disomy in the clinical diagnostic laboratory.

Ngo C, Baluyot M, Bennetts B, Carmichael J, Clark A, Darmanian A, Gayagay T, Jones L, Nash B, Clark M, Jose N, Robinson S, St Heaps L, Wright D. Ngo C, et al. Among authors: darmanian a. Pathology. 2023 Oct;55(6):818-826. doi: 10.1016/j.pathol.2023.04.004. Epub 2023 Jun 16. Pathology. 2023. PMID: 37414616

4

Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalances.

Daniel A, Baker E, Chia N, Haan E, Malafiej P, Hinton L, Clarke N, Adès L, Darmanian A, Callen D. Daniel A, et al. Among authors: darmanian a. Am J Med Genet A. 2003 Feb 15;117A(1):57-64. doi: 10.1002/ajmg.a.10048. Am J Med Genet A. 2003. PMID: 12548741 Review.

5

Three different origins for apparent triploid/diploid mosaics.

Daniel A, Wu Z, Darmanian A, Collins F, Jackson J. Daniel A, et al. Among authors: darmanian a. Prenat Diagn. 2003 Jul;23(7):529-34. doi: 10.1002/pd.634. Prenat Diagn. 2003. PMID: 12868076

6

Validation of a Chromosomal Microarray for Prenatal Diagnosis Using a Prospective Cohort of Pregnancies with Increased Risk for Chromosome Abnormalities.

Wright D, Carey L, Battersby S, Nguyen T, Clarke M, Nash B, Gulesserian E, Cross J, Darmanian A. Wright D, et al. Among authors: darmanian a. Genet Test Mol Biomarkers. 2016 Dec;20(12):791-798. doi: 10.1089/gtmb.2016.0117. Epub 2016 Sep 30. Genet Test Mol Biomarkers. 2016. PMID: 27690282

7

Neuroblastoma Molecular Risk-Stratification of DNA Copy Number and ALK Genotyping via Cell-Free Circulating Tumor DNA Profiling.

Kahana-Edwin S, Cain LE, McCowage G, Darmanian A, Wright D, Mullins A, Saletta F, Karpelowsky J. Kahana-Edwin S, et al. Among authors: darmanian a. Cancers (Basel). 2021 Jul 5;13(13):3365. doi: 10.3390/cancers13133365. Cancers (Basel). 2021. PMID: 34282791 Free PMC article.

8

14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.

Ellaway CJ, Ho G, Bettella E, Knapman A, Collins F, Hackett A, McKenzie F, Darmanian A, Peters GB, Fagan K, Christodoulou J. Ellaway CJ, et al. Among authors: darmanian a. Eur J Hum Genet. 2013 May;21(5):522-7. doi: 10.1038/ejhg.2012.208. Epub 2012 Sep 12. Eur J Hum Genet. 2013. PMID: 22968132 Free PMC article.

9

Cyclin-dependent kinase-like 5 (CDKL5) mutation screening in Rett syndrome and related disorders.

White R, Ho G, Schmidt S, Scheffer IE, Fischer A, Yendle SC, Bienvenu T, Nectoux J, Ellaway CJ, Darmanian A, Tong X, Cloosterman D, Bennetts B, Kalra V, Fullston T, Gecz J, Cox TC, Christodoulou J. White R, et al. Among authors: darmanian a. Twin Res Hum Genet. 2010 Apr;13(2):168-78. doi: 10.1375/twin.13.2.168. Twin Res Hum Genet. 2010. PMID: 20397747

10

A melanoma-associated germline mutation in exon 1beta inactivates p14ARF.

Rizos H, Puig S, Badenas C, Malvehy J, Darmanian AP, Jiménez L, Milà M, Kefford RF. Rizos H, et al. Among authors: darmanian ap. Oncogene. 2001 Sep 6;20(39):5543-7. doi: 10.1038/sj.onc.1204728. Oncogene. 2001. PMID: 11571653

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