Sleiman P - Search Results

1

Assessing non-Mendelian inheritance in inherited axonopathies.

Bis-Brewer DM, Gan-Or Z, Sleiman P; Inherited Neuropathy Consortium; Hakonarson H, Fazal S, Courel S, Cintra V, Tao F, Estiar MA, Tarnopolsky M, Boycott KM, Yoon G, Suchowersky O, Dupré N, Cheng A, Lloyd TE, Rouleau G, Schüle R, Züchner S. Bis-Brewer DM, et al. Among authors: sleiman p. Genet Med. 2020 Dec;22(12):2114-2119. doi: 10.1038/s41436-020-0924-0. Epub 2020 Aug 3. Genet Med. 2020. PMID: 32741968 Free PMC article.

2

Genetic underpinnings of obstructive sleep apnea: are we making progress?

Sleiman P, Hakonarson H. Sleiman P, et al. Sleep. 2011 Nov 1;34(11):1449-52. doi: 10.5665/sleep.1366. Sleep. 2011. PMID: 22043111 Free PMC article. No abstract available.

3

Assessing the functional consequence of loss of function variants using electronic medical record and large-scale genomics consortium efforts.

Sleiman P, Bradfield J, Mentch F, Almoguera B, Connolly J, Hakonarson H. Sleiman P, et al. Front Genet. 2014 Apr 29;5:105. doi: 10.3389/fgene.2014.00105. eCollection 2014. Front Genet. 2014. PMID: 24808909 Free PMC article.

4

Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes.

Almoguera B, Vazquez L, Connolly JJ, Bradfield J, Sleiman P, Keating B, Hakonarson H. Almoguera B, et al. Among authors: sleiman p. Front Genet. 2014 May 12;5:96. doi: 10.3389/fgene.2014.00096. eCollection 2014. Front Genet. 2014. PMID: 24860591 Free PMC article.

5

From schizophrenia risk locus to schizophrenia genes.

Sleiman P, Hakonarson H. Sleiman P, et al. Nat Med. 2016 Jun 7;22(6):583-4. doi: 10.1038/nm.4122. Nat Med. 2016. PMID: 27270776 No abstract available.

6

Examination of genetic variants influencing lipid traits in pediatric populations.

Wang K, Zhang H, Mentch FD, Bradfield JP, Glessner JT, Qiu H, Guo Y, Hou C, Frackelton EC, Thomas K, Bender A, Albano A, Otieno G, Garris M, Seidler K, Moy A, Kim CE, Keating B, Chiavacci RM, Grundmeier R, Sleiman PA, Grant SF, Hakonarson H. Wang K, et al. Among authors: sleiman pa. J Pediatr Genet. 2012 Jun;1(2):85-98. doi: 10.3233/PGE-2012-016. J Pediatr Genet. 2012. PMID: 27625808 Free PMC article.

7

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.

Chang X, Zhao Y, Hou C, Glessner J, McDaniel L, Diamond MA, Thomas K, Li J, Wei Z, Liu Y, Guo Y, Mentch FD, Qiu H, Kim C, Evans P, Vaksman Z, Diskin SJ, Attiyeh EF, Sleiman P, Maris JM, Hakonarson H. Chang X, et al. Among authors: sleiman p. Nat Commun. 2017 Sep 18;8(1):569. doi: 10.1038/s41467-017-00408-8. Nat Commun. 2017. PMID: 28924153 Free PMC article.

8

Bayesian analysis of genome-wide inflammatory bowel disease data sets reveals new risk loci.

Zhang Y, Tian L, Sleiman P, Ghosh S, Hakonarson H; International IBD Genetics Consortium. Zhang Y, et al. Among authors: sleiman p. Eur J Hum Genet. 2018 Feb;26(2):265-274. doi: 10.1038/s41431-017-0041-y. Epub 2017 Dec 4. Eur J Hum Genet. 2018. PMID: 29203833 Free PMC article.

9

Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964).

Chang X, Li D, Tian L, Liu Y, March M, Wang T, Hou C, Pellegrino R, Levy R, Jen M, Soccio R, Sleiman P, Hakonarson H, Castelo-Soccio L. Chang X, et al. Among authors: sleiman p. J Pediatr. 2018 Mar;194:248-252.e2. doi: 10.1016/j.jpeds.2017.11.011. Epub 2017 Dec 18. J Pediatr. 2018. PMID: 29269196

10

Non-coding RNA dysregulation in the amygdala region of schizophrenia patients contributes to the pathogenesis of the disease.

Liu Y, Chang X, Hahn CG, Gur RE, Sleiman PAM, Hakonarson H. Liu Y, et al. Transl Psychiatry. 2018 Feb 2;8(1):44. doi: 10.1038/s41398-017-0030-5. Transl Psychiatry. 2018. PMID: 29391398 Free PMC article.

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