Rouleau GA - Search Results

1

Adenylosuccinate lyase (ADSL) and infantile autism: absence of previously reported point mutation.

Fon EA, Sarrazin J, Meunier C, Alarcia J, Shevell MI, Philippe A, Leboyer M, Rouleau GA. Fon EA, et al. Among authors: rouleau ga. Am J Med Genet. 1995 Dec 18;60(6):554-7. doi: 10.1002/ajmg.1320600614. Am J Med Genet. 1995. PMID: 8825895

2

Mapping of the human adenylosuccinate lyase (ADSL) gene to chromosome 22q13.1-->q13.2.

Fon EA, Demczuk S, Delattre O, Thomas G, Rouleau GA. Fon EA, et al. Among authors: rouleau ga. Cytogenet Cell Genet. 1993;64(3-4):201-3. doi: 10.1159/000133575. Cytogenet Cell Genet. 1993. PMID: 8404037

3

Loss of heterozygosity on chromosome 22 in human gliomas does not inactivate the neurofibromatosis type 2 gene.

Watkins D, Ruttledge MH, Sarrazin J, Rangaratnam S, Poisson M, Delattre JY, Rouleau GA. Watkins D, et al. Among authors: rouleau ga. Cancer Genet Cytogenet. 1996 Nov;92(1):73-8. doi: 10.1016/s0165-4608(96)00149-5. Cancer Genet Cytogenet. 1996. PMID: 8956876

4

Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3.

Lafrenière RG, Kibar Z, Rochefort DL, Han FY, Fon EA, Dubé MP, Kang X, Baird S, Korneluk RG, Rommens JM, Rouleau GA. Lafrenière RG, et al. Among authors: rouleau ga. Gene. 1997 Oct 1;198(1-2):313-21. doi: 10.1016/s0378-1119(97)00333-8. Gene. 1997. PMID: 9370297

5

Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3.

Lafrenière RG, Rochefort DL, Kibar Z, Fon EA, Han F, Cochius J, Kang X, Baird S, Korneluk RG, Andermann E, Rommens JM, Rouleau GA. Lafrenière RG, et al. Among authors: rouleau ga. Genomics. 1996 Dec 15;38(3):264-72. doi: 10.1006/geno.1996.0627. Genomics. 1996. PMID: 8975701

6

Apolipoprotein E genotype in schizophrenia.

Joober R, Rouleau G, Fon E, Lal S, Palmour R, Bloom D, Labelle A, Benkelfat C. Joober R, et al. Am J Med Genet. 1996 Apr 9;67(2):235. doi: 10.1002/ajmg.1320670204. Am J Med Genet. 1996. PMID: 8723056 No abstract available.

7

Identification of three polymorphisms in the translated region of PLC-gamma1 and their investigation in lithium responsive bipolar disorder.

Ftouhi-Paquin N, Alda M, Grof P, Chretien N, Rouleau G, Turecki G. Ftouhi-Paquin N, et al. Am J Med Genet. 2001 Apr 8;105(3):301-5. doi: 10.1002/ajmg.1326. Am J Med Genet. 2001. PMID: 11353454

8

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.

Daoud H, Valdmanis PN, Kabashi E, Dion P, Dupré N, Camu W, Meininger V, Rouleau GA. Daoud H, et al. Among authors: rouleau ga. J Med Genet. 2009 Feb;46(2):112-4. doi: 10.1136/jmg.2008.062463. Epub 2008 Oct 17. J Med Genet. 2009. PMID: 18931000

9

Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.

Pramatarova A, Figlewicz DA, Krizus A, Han FY, Ceballos-Picot I, Nicole A, Dib M, Meininger V, Brown RH, Rouleau GA. Pramatarova A, et al. Among authors: rouleau ga. Am J Hum Genet. 1995 Mar;56(3):592-6. Am J Hum Genet. 1995. PMID: 7887412 Free PMC article.

10

Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease.

Ruttledge MH, Andermann AA, Phelan CM, Claudio JO, Han FY, Chretien N, Rangaratnam S, MacCollin M, Short P, Parry D, Michels V, Riccardi VM, Weksberg R, Kitamura K, Bradburn JM, Hall BD, Propping P, Rouleau GA. Ruttledge MH, et al. Among authors: rouleau ga. Am J Hum Genet. 1996 Aug;59(2):331-42. Am J Hum Genet. 1996. PMID: 8755919 Free PMC article.

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