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Family-based association study of TPH1 and TPH2 polymorphisms in autism.
Ramoz N, Cai G, Reichert JG, Corwin TE, Kryzak LA, Smith CJ, Silverman JM, Hollander E, Buxbaum JD. Ramoz N, et al. Among authors: silverman jm. Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):861-7. doi: 10.1002/ajmg.b.30356. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16958027
Symptom domains in autism and related conditions: evidence for familiality.
Silverman JM, Smith CJ, Schmeidler J, Hollander E, Lawlor BA, Fitzgerald M, Buxbaum JD, Delaney K, Galvin P; Autism Genetic Research Exchange Consortium. Silverman JM, et al. Am J Med Genet. 2002 Jan 8;114(1):64-73. doi: 10.1002/ajmg.10048. Am J Med Genet. 2002. PMID: 11840508
Association between a GABRB3 polymorphism and autism.
Buxbaum JD, Silverman JM, Smith CJ, Greenberg DA, Kilifarski M, Reichert J, Cook EH Jr, Fang Y, Song CY, Vitale R. Buxbaum JD, et al. Among authors: silverman jm. Mol Psychiatry. 2002;7(3):311-6. doi: 10.1038/sj.mp.4001011. Mol Psychiatry. 2002. PMID: 11920158
Phenotypic features of myoclonus-dystonia in three kindreds.
Doheny DO, Brin MF, Morrison CE, Smith CJ, Walker RH, Abbasi S, Müller B, Garrels J, Liu L, De Carvalho Aguiar P, Schilling K, Kramer P, De Leon D, Raymond D, Saunders-Pullman R, Klein C, Bressman SB, Schmand B, Tijssen MA, Ozelius LJ, Silverman JM. Doheny DO, et al. Among authors: silverman jm. Neurology. 2002 Oct 22;59(8):1187-96. doi: 10.1212/wnl.59.8.1187. Neurology. 2002. PMID: 12391346
342 results