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Retinoblastoma genetics screening and clinical management.
BMC Med Genomics. 2021 Jul 22;14(1):188. doi: 10.1186/s12920-021-01034-6.
BMC Med Genomics. 2021.
PMID: 34294096
Free PMC article.
The GenomeAsia 100K Project enables genetic discoveries across Asia.
GenomeAsia100K Consortium.
GenomeAsia100K Consortium.
Nature. 2019 Dec;576(7785):106-111. doi: 10.1038/s41586-019-1793-z. Epub 2019 Dec 4.
Nature. 2019.
PMID: 31802016
Free PMC article.
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Myoneuropathic presentation of limb girdle muscular dystrophy R8 with a novel TRIM32 mutation.
Chandrasekharan SV, Sundaram S, Malaichamy S, Poyuran R, Nair SS.
Chandrasekharan SV, et al. Among authors: malaichamy s.
Neuromuscul Disord. 2021 Sep;31(9):886-890. doi: 10.1016/j.nmd.2021.06.003. Epub 2021 Jun 11.
Neuromuscul Disord. 2021.
PMID: 34244021
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Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness.
Neuillé M, Malaichamy S, Vadalà M, Michiels C, Condroyer C, Sachidanandam R, Srilekha S, Arokiasamy T, Letexier M, Démontant V, Sahel JA, Sen P, Audo I, Soumittra N, Zeitz C.
Neuillé M, et al. Among authors: malaichamy s.
Clin Genet. 2016 Jun;89(6):690-9. doi: 10.1111/cge.12746. Epub 2016 Mar 4.
Clin Genet. 2016.
PMID: 26822852
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Molecular profiling of complete congenital stationary night blindness: a pilot study on an Indian cohort.
Malaichamy S, Sen P, Sachidanandam R, Arokiasamy T, Lancelot ME, Audo I, Zeitz C, Soumittra N.
Malaichamy S, et al.
Mol Vis. 2014 Mar 21;20:341-51. eCollection 2014.
Mol Vis. 2014.
PMID: 24715752
Free PMC article.
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Identification of African-Specific Admixture between Modern and Archaic Humans.
Wall JD, Ratan A, Stawiski E; GenomeAsia 100K Consortium.
Wall JD, et al.
Am J Hum Genet. 2019 Dec 5;105(6):1254-1261. doi: 10.1016/j.ajhg.2019.11.005.
Am J Hum Genet. 2019.
PMID: 31809748
Free PMC article.
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