Haller G - Search Results

1

Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy.

Sadler B, Haller G, Agrawal A, Culverhouse R, Bucholz K, Brooks A, Tischfield J, Johnson EO, Edenberg H, Schuckit M, Saccone N, Bierut L, Goate A. Sadler B, et al. Among authors: haller g. Sci Rep. 2014 Mar 28;4:4497. doi: 10.1038/srep04497. Sci Rep. 2014. PMID: 24675634 Free PMC article.

2

Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence.

Haller G, Druley T, Vallania FL, Mitra RD, Li P, Akk G, Steinbach JH, Breslau N, Johnson E, Hatsukami D, Stitzel J, Bierut LJ, Goate AM. Haller G, et al. Hum Mol Genet. 2012 Feb 1;21(3):647-55. doi: 10.1093/hmg/ddr498. Epub 2011 Oct 31. Hum Mol Genet. 2012. PMID: 22042774 Free PMC article.

3

Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence.

Haller G, Kapoor M, Budde J, Xuei X, Edenberg H, Nurnberger J, Kramer J, Brooks A, Tischfield J, Almasy L, Agrawal A, Bucholz K, Rice J, Saccone N, Bierut L, Goate A. Haller G, et al. Hum Mol Genet. 2014 Feb 1;23(3):810-9. doi: 10.1093/hmg/ddt463. Epub 2013 Sep 20. Hum Mol Genet. 2014. PMID: 24057674 Free PMC article.

4

Functional characterization improves associations between rare non-synonymous variants in CHRNB4 and smoking behavior.

Haller G, Li P, Esch C, Hsu S, Goate AM, Steinbach JH. Haller G, et al. PLoS One. 2014 May 7;9(5):e96753. doi: 10.1371/journal.pone.0096753. eCollection 2014. PLoS One. 2014. PMID: 24804708 Free PMC article.

5

Positive Selection on Loci Associated with Drug and Alcohol Dependence.

Sadler B, Haller G, Edenberg H, Tischfield J, Brooks A, Kramer J, Schuckit M, Nurnberger J, Goate A. Sadler B, et al. Among authors: haller g. PLoS One. 2015 Aug 13;10(8):e0134393. doi: 10.1371/journal.pone.0134393. eCollection 2015. PLoS One. 2015. PMID: 26270548 Free PMC article.

6

A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis.

Haller G, Alvarado D, Mccall K, Yang P, Cruchaga C, Harms M, Goate A, Willing M, Morcuende JA, Baschal E, Miller NH, Wise C, Dobbs MB, Gurnett CA. Haller G, et al. Hum Mol Genet. 2016 Jan 1;25(1):202-9. doi: 10.1093/hmg/ddv463. Epub 2015 Nov 12. Hum Mol Genet. 2016. PMID: 26566670 Free PMC article.

7

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis.

Haller G, McCall K, Jenkitkasemwong S, Sadler B, Antunes L, Nikolov M, Whittle J, Upshaw Z, Shin J, Baschal E, Cruchaga C, Harms M, Raggio C, Morcuende JA, Giampietro P, Miller NH, Wise C, Gray RS, Solnica-Krezel L, Knutson M, Dobbs MB, Gurnett CA. Haller G, et al. Nat Commun. 2018 Oct 9;9(1):4171. doi: 10.1038/s41467-018-06705-0. Nat Commun. 2018. PMID: 30301978 Free PMC article.

8

von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene.

Sadler B, Christopherson PA, Haller G, Montgomery RR, Di Paola J. Sadler B, et al. Among authors: haller g. Blood. 2021 Jun 10;137(23):3277-3283. doi: 10.1182/blood.2020009999. Blood. 2021. PMID: 33556167 Free PMC article. Clinical Trial.

9

Elucidating the Genetic Basis of Chiari I Malformation.

Haller G, Sadler B. Haller G, et al. Neurosurg Clin N Am. 2023 Jan;34(1):55-60. doi: 10.1016/j.nec.2022.07.001. Neurosurg Clin N Am. 2023. PMID: 36424064 Review.

10

Characterization of copy-number variants in a large cohort of patients with von Willebrand disease reveals a relationship between disrupted regions and disease type.

Sadler B, Christopherson PA, Perry CL, Bellissimo DB, Haberichter SL, Haller G, Antunes L, Flood VH, Di Paola J, Montgomery RR; Zimmerman Program Investigators. Sadler B, et al. Among authors: haller g. Res Pract Thromb Haemost. 2023 Oct 14;7(7):102232. doi: 10.1016/j.rpth.2023.102232. eCollection 2023 Oct. Res Pract Thromb Haemost. 2023. PMID: 38077814 Free PMC article.

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