CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

Rees, E (author)

Walters, JTR (author)

Chambert, KD (author)

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O'Dushlaine, C (author)

Szatkiewicz, J (author)

Richards, AL (author)

Georgieva, L (author)

Mahoney-Davies, G (author)

Legge, SE (author)

Moran, JL (author)

Genovese, G (author)

Levinson, D (author)

Morris, DW (author)

Cormican, P (author)

Kendler, KS (author)

O'Neill, FA (author)

Riley, B (author)

Gill, M (author)

Corvin, A (author)

Sklar, P (author)

Hultman, C (author)

Karolinska Institutet

Pato, C (author)

Pato, M (author)

Sullivan, PF (author)

Karolinska Institutet

Gejman, PV (author)

McCarroll, SA (author)

O'Donovan, MC (author)

Owen, MJ (author)

Kirov, G (author)

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 (creator_code:org_t)

2013-10-26

2014

English.

In: Human molecular genetics. - : Oxford University Press (OUP). - 1460-2083 .- 0964-6906. ; 23:6, s. 1669-1676

Related links:

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• Journal article (peer-reviewed)