Abul-Husn NS - Search Results

1

Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35.

Cullina S, Wojcik GL, Shemirani R, Klarin D, Gorman BR, Sorokin EP, Gignoux CR, Belbin GM, Pyarajan S, Asgari S, Tsao PS, Damrauer SM, Abul-Husn NS, Kenny EE. Cullina S, et al. Among authors: abul husn ns. Front Genet. 2023 Aug 1;14:1181167. doi: 10.3389/fgene.2023.1181167. eCollection 2023. Front Genet. 2023. PMID: 37600667 Free PMC article.

2

Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system.

Belbin GM, Odgis J, Sorokin EP, Yee MC, Kohli S, Glicksberg BS, Gignoux CR, Wojcik GL, Van Vleck T, Jeff JM, Linderman M, Schurmann C, Ruderfer D, Cai X, Merkelson A, Justice AE, Young KL, Graff M, North KE, Peters U, James R, Hindorff L, Kornreich R, Edelmann L, Gottesman O, Stahl EE, Cho JH, Loos RJ, Bottinger EP, Nadkarni GN, Abul-Husn NS, Kenny EE. Belbin GM, et al. Elife. 2017 Sep 12;6:e25060. doi: 10.7554/eLife.25060. Elife. 2017. PMID: 28895531 Free PMC article.

3

Personalized Medicine and the Power of Electronic Health Records.

Abul-Husn NS, Kenny EE. Abul-Husn NS, et al. Cell. 2019 Mar 21;177(1):58-69. doi: 10.1016/j.cell.2019.02.039. Cell. 2019. PMID: 30901549 Free PMC article. Review.

4

Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry.

Damrauer SM, Chaudhary K, Cho JH, Liang LW, Argulian E, Chan L, Dobbyn A, Guerraty MA, Judy R, Kay J, Kember RL, Levin MG, Saha A, Van Vleck T, Verma SS, Weaver J, Abul-Husn NS, Baras A, Chirinos JA, Drachman B, Kenny EE, Loos RJF, Narula J, Overton J, Reid J, Ritchie M, Sirugo G, Nadkarni G, Rader DJ, Do R. Damrauer SM, et al. JAMA. 2019 Dec 10;322(22):2191-2202. doi: 10.1001/jama.2019.17935. JAMA. 2019. PMID: 31821430 Free PMC article.

5

Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank.

Abul-Husn NS, Soper ER, Odgis JA, Cullina S, Bobo D, Moscati A, Rodriguez JE; CBIPM Genomics Team; Regeneron Genetics Center; Loos RJF, Cho JH, Belbin GM, Suckiel SA, Kenny EE. Abul-Husn NS, et al. Genome Med. 2019 Dec 31;12(1):2. doi: 10.1186/s13073-019-0691-1. Genome Med. 2019. PMID: 31892343 Free PMC article.

6

A common variant in PNPLA3 is associated with age at diagnosis of NAFLD in patients from a multi-ethnic biobank.

Walker RW, Belbin GM, Sorokin EP, Van Vleck T, Wojcik GL, Moscati A, Gignoux CR, Cho J, Abul-Husn NS, Nadkarni G, Kenny EE, Loos RJF. Walker RW, et al. J Hepatol. 2020 Jun;72(6):1070-1081. doi: 10.1016/j.jhep.2020.01.029. Epub 2020 Mar 5. J Hepatol. 2020. PMID: 32145261 Free PMC article.

7

COVID-19 outcomes and the human genome.

Murray MF, Kenny EE, Ritchie MD, Rader DJ, Bale AE, Giovanni MA, Abul-Husn NS. Murray MF, et al. Genet Med. 2020 Jul;22(7):1175-1177. doi: 10.1038/s41436-020-0832-3. Epub 2020 May 12. Genet Med. 2020. PMID: 32393819 Free PMC article. No abstract available.

8

Lynch Syndrome-Associated Variants and Cancer Rates in an Ancestrally Diverse Biobank.

Rosenblum RE, Ang C, Suckiel SA, Soper ER, Sigireddi MR, Cullina S, Belbin GM, Lucas AL, Kenny EE, Abul-Husn NS. Rosenblum RE, et al. JCO Precis Oncol. 2020 Nov 23;4:PO.20.00290. doi: 10.1200/PO.20.00290. eCollection 2020. JCO Precis Oncol. 2020. PMID: 33283134 Free PMC article.

9

Genomic Screening Identifies Individuals at High Risk for Hereditary Transthyretin Amyloidosis.

Soper ER, Suckiel SA, Braganza GT, Kontorovich AR, Kenny EE, Abul-Husn NS. Soper ER, et al. J Pers Med. 2021 Jan 15;11(1):49. doi: 10.3390/jpm11010049. J Pers Med. 2021. PMID: 33467513 Free PMC article.

10

GUÍA: a digital platform to facilitate result disclosure in genetic counseling.

Suckiel SA, Odgis JA, Gallagher KM, Rodriguez JE, Watnick D, Bertier G, Sebastin M, Yelton N, Maria E, Lopez J, Ramos M, Kelly N, Teitelman N, Beren F, Kaszemacher T, Davis K, Laguerre I, Richardson LD, Diaz GA, Pearson NM, Ellis SB, Stolte C, Robinson M, Kovatch P, Horowitz CR, Gelb BD, Greally JM, Bauman LJ, Zinberg RE, Abul-Husn NS, Wasserstein MP, Kenny EE. Suckiel SA, et al. Genet Med. 2021 May;23(5):942-949. doi: 10.1038/s41436-020-01063-z. Epub 2021 Feb 2. Genet Med. 2021. PMID: 33531665 Free PMC article. Clinical Trial.

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