Moses E - Search Results

1

Prevalence of common sleep disorders in a middle-aged community sample.

McArdle N, Reynolds AC, Hillman D, Moses E, Maddison K, Melton P, Eastwood P. McArdle N, et al. Among authors: moses e. J Clin Sleep Med. 2022 Jun 1;18(6):1503-1514. doi: 10.5664/jcsm.9886. J Clin Sleep Med. 2022. PMID: 35082023 Free PMC article.

2

Genome-wide association study of autistic-like traits in a general population study of young adults.

Jones RM, Cadby G, Melton PE, Abraham LJ, Whitehouse AJ, Moses EK. Jones RM, et al. Among authors: moses ek. Front Hum Neurosci. 2013 Oct 11;7:658. doi: 10.3389/fnhum.2013.00658. eCollection 2013. Front Hum Neurosci. 2013. PMID: 24133439 Free PMC article.

3

Meta-analysis of human methylation data for evidence of sex-specific autosomal patterns.

McCarthy NS, Melton PE, Cadby G, Yazar S, Franchina M, Moses EK, Mackey DA, Hewitt AW. McCarthy NS, et al. Among authors: moses ek. BMC Genomics. 2014 Nov 18;15(1):981. doi: 10.1186/1471-2164-15-981. BMC Genomics. 2014. PMID: 25406947 Free PMC article.

4

Absence of germline mutations in BAP1 in sporadic cases of malignant mesothelioma.

Sneddon S, Leon JS, Dick IM, Cadby G, Olsen N, Brims F, Allcock RJ, Moses EK, Melton PE, de Klerk N, Musk AW, Robinson BW, Creaney J. Sneddon S, et al. Among authors: moses ek. Gene. 2015 May 25;563(1):103-5. doi: 10.1016/j.gene.2015.03.031. Epub 2015 Mar 18. Gene. 2015. PMID: 25796603 Free article.

5

Genome-wide transcriptome directed pathway analysis of maternal pre-eclampsia susceptibility genes.

Yong HE, Melton PE, Johnson MP, Freed KA, Kalionis B, Murthi P, Brennecke SP, Keogh RJ, Moses EK. Yong HE, et al. Among authors: moses ek. PLoS One. 2015 May 26;10(5):e0128230. doi: 10.1371/journal.pone.0128230. eCollection 2015. PLoS One. 2015. PMID: 26010865 Free PMC article. Clinical Trial.

6

The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia.

Thomsen LC, McCarthy NS, Melton PE, Cadby G, Austgulen R, Nygård OK, Johnson MP, Brennecke S, Moses EK, Bjørge L, Iversen AC. Thomsen LC, et al. Among authors: moses ek. J Hypertens. 2017 Jan;35(1):132-139. doi: 10.1097/HJH.0000000000001131. J Hypertens. 2017. PMID: 27755385 Free PMC article.

7

Exome array analysis suggests an increased variant burden in families with schizophrenia.

McCarthy NS, Melton PE, Ward SV, Allan SM, Dragovic M, Clark ML, Morar B, Rubio JP, Blangero J, Badcock JC, Morgan VA, Moses EK, Jablensky A. McCarthy NS, et al. Among authors: moses ek. Schizophr Res. 2017 Jul;185:9-16. doi: 10.1016/j.schres.2016.12.007. Epub 2016 Dec 9. Schizophr Res. 2017. PMID: 27939555

8

Assessment of Cognition and Personality as Potential Endophenotypes in the Western Australian Family Study of Schizophrenia.

McCarthy NS, Badcock JC, Clark ML, Knowles EEM, Cadby G, Melton PE, Morgan VA, Blangero J, Moses EK, Glahn DC, Jablensky A. McCarthy NS, et al. Among authors: moses ek. Schizophr Bull. 2018 Jun 6;44(4):908-921. doi: 10.1093/schbul/sbx141. Schizophr Bull. 2018. PMID: 29040798 Free PMC article.

9

Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study.

Cadby G, Melton PE, McCarthy NS, Almeida M, Williams-Blangero S, Curran JE, VandeBerg JL, Hui J, Beilby J, Musk AW, James AL, Hung J, Blangero J, Moses EK. Cadby G, et al. Among authors: moses ek. Hum Genet. 2018 Jan;137(1):45-53. doi: 10.1007/s00439-017-1856-x. Epub 2017 Nov 27. Hum Genet. 2018. PMID: 29181734

10

Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity.

Khan FF, Melton PE, McCarthy NS, Morar B, Blangero J, Moses EK, Jablensky A. Khan FF, et al. Among authors: moses ek. Schizophr Res. 2018 Jul;197:337-345. doi: 10.1016/j.schres.2018.02.034. Epub 2018 Feb 24. Schizophr Res. 2018. PMID: 29486958 Free article.

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