Genome Québec/International[Grants and Funding] - Search Results

Year	Number of Results
2018	6
2019	4
2020	1
2021	1
2024	0

1

Can Cyanobacterial Diversity in the Source Predict the Diversity in Sludge and the Risk of Toxin Release in a Drinking Water Treatment Plant?

Jalili F, Trigui H, Guerra Maldonado JF, Dorner S, Zamyadi A, Shapiro BJ, Terrat Y, Fortin N, Sauvé S, Prévost M. Jalili F, et al. Toxins (Basel). 2021 Jan 1;13(1):25. doi: 10.3390/toxins13010025. Toxins (Basel). 2021. PMID: 33401450 Free PMC article.

2

Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further research.

Innes AM, McInnes BL, Dyment DA. Innes AM, et al. Am J Med Genet C Semin Med Genet. 2018 Dec;178(4):387-397. doi: 10.1002/ajmg.c.31661. Am J Med Genet C Semin Med Genet. 2018. PMID: 30580484

3

Functions of stone cells and oleoresin terpenes in the conifer defense syndrome.

Whitehill JGA, Yuen MMS, Henderson H, Madilao L, Kshatriya K, Bryan J, Jaquish B, Bohlmann J. Whitehill JGA, et al. New Phytol. 2019 Feb;221(3):1503-1517. doi: 10.1111/nph.15477. Epub 2018 Oct 23. New Phytol. 2019. PMID: 30216451 Free article.

4

NID1 variant associated with occipital cephaloceles in a family expressing a spectrum of phenotypes.

McNiven V, Ito YA, Hartley T, Kernohan K, Miller E; Care4Rare Canada; Armour CM. McNiven V, et al. Am J Med Genet A. 2019 May;179(5):837-841. doi: 10.1002/ajmg.a.61095. Epub 2019 Feb 17. Am J Med Genet A. 2019. PMID: 30773799

5

Testing association of rare genetic variants with resistance to three common antiseizure medications.

Wolking S, Moreau C, Nies AT, Schaeffeler E, McCormack M, Auce P, Avbersek A, Becker F, Krenn M, Møller RS, Nikanorova M, Weber YG, Weckhuysen S, Cavalleri GL, Delanty N, Depondt C, Johnson MR, Koeleman BPC, Kunz WS, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Schwab M, Krause R, Sisodiya SM, Cossette P, Girard SL, Lerche H; EpiPGX Consortium. Wolking S, et al. Epilepsia. 2020 Apr;61(4):657-666. doi: 10.1111/epi.16467. Epub 2020 Mar 6. Epilepsia. 2020. PMID: 32141622 Free article.

6

Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in males.

Ambalavanan A, Chaumette B, Zhou S, Xie P, He Q, Spiegelman D, Dionne-Laporte A, Bourassa CV, Therrien M, Rochefort D, Xiong L, Dion PA, Joober R, Rapoport JL, Girard SL, Rouleau GA. Ambalavanan A, et al. Am J Med Genet B Neuropsychiatr Genet. 2019 Sep;180(6):335-340. doi: 10.1002/ajmg.b.32683. Epub 2018 Oct 30. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30378261

7

Neu-Laxova syndrome presenting prenatally with increased nuchal translucency and cystic hygroma: The utility of exome sequencing in deciphering the diagnosis.

Bourque DK, Cloutier M, Kernohan KD, Bareke E, Grynspan D, Michaud J; Care4Rare Canada Consortium; Boycott KM. Bourque DK, et al. Am J Med Genet A. 2019 May;179(5):813-816. doi: 10.1002/ajmg.a.61076. Epub 2019 Mar 5. Am J Med Genet A. 2019. PMID: 30838783

8

The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®.

Hartley T, Balcı TB, Rojas SK, Eaton A, Canada CR, Dyment DA, Boycott KM. Hartley T, et al. Am J Med Genet C Semin Med Genet. 2018 Dec;178(4):458-463. doi: 10.1002/ajmg.c.31662. Am J Med Genet C Semin Med Genet. 2018. PMID: 30580481

9

A Discrete Event Simulation Model to Assess the Economic Value of a Hypothetical Pharmacogenomics Test for Statin-Induced Myopathy in Patients Initiating a Statin in Secondary Cardiovascular Prevention.

Mitchell D, Guertin JR, Dubois A, Dubé MP, Tardif JC, Iliza AC, Fanton-Aita F, Matteau A, LeLorier J. Mitchell D, et al. Mol Diagn Ther. 2018 Apr;22(2):241-254. doi: 10.1007/s40291-018-0323-2. Mol Diagn Ther. 2018. PMID: 29651791 Free article.

10

Mosaic KRAS mutation in a patient with encephalocraniocutaneous lipomatosis and renovascular hypertension.

McDonell LM, Leung GK, Daoud H, Ip J, Chim S, Luk HM, Lan L; Care4Rare Canada Consortium; Boycott KM, Chung BH. McDonell LM, et al. Am J Med Genet A. 2018 Nov;176(11):2523-2527. doi: 10.1002/ajmg.a.40349. Epub 2018 Oct 5. Am J Med Genet A. 2018. PMID: 30289595 No abstract available.

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