Erratum: Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630))

Daniel Moreno-De-Luca; Jennifer G. Mulle; Erin B. Kaminsky; Stephan J. Sanders; Scott M. Myers; Margaret P. Adam; Amy T. Pakula; Nancy J. Eisenhauer; Kim Uhas; Luann Weik; Lisa Guy; Melanie E. Care; Chantal F. Morel; Charlotte Boni; Bonnie Anne Salbert; Ashadeep Chandrareddy; Laurie A. Demmer; Eva W.C. Chow; Urvashi Surti; Swaroop Aradhya; Diane L. Pickering; Denae M. Golden; Warren G. Sanger; Emily Aston; Arthur R. Brothman; Troy J. Gliem; Erik C. Thorland; Todd Ackley; Ram Iyer; Shuwen Huang; John C. Barber; John A. Crolla; Stephen T. Warren; Christa L. Martin; David H. Ledbetter

doi:10.1016/j.ajhg.2010.12.005

Erratum: Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630))

Daniel Moreno-De-Luca, Jennifer G. Mulle, Erin B. Kaminsky, Stephan J. Sanders, Scott M. Myers, Margaret P. Adam, Amy T. Pakula, Nancy J. Eisenhauer, Kim Uhas, Luann Weik, Lisa Guy, Melanie E. Care, Chantal F. Morel, Charlotte Boni, Bonnie Anne Salbert, Ashadeep Chandrareddy, Laurie A. Demmer, Eva W.C. Chow, Urvashi Surti, Swaroop AradhyaDiane L. Pickering, Denae M. Golden, Warren G. Sanger, Emily Aston, Arthur R. Brothman, Troy J. Gliem, Erik C. Thorland, Todd Ackley, Ram Iyer, Shuwen Huang, John C. Barber, John A. Crolla, Stephen T. Warren, Christa L. Martin, David H. Ledbetter

Research output: Contribution to journal › Comment/debate › peer-review

2 Scopus citations

Original language	English (US)
Pages (from-to)	121
Number of pages	1
Journal	American Journal of Human Genetics
Volume	88
Issue number	1
DOIs	https://doi.org/10.1016/j.ajhg.2010.12.005
State	Published - Jan 7 2011
Externally published	Yes

ASJC Scopus subject areas

Genetics
Genetics(clinical)

Access to Document

10.1016/j.ajhg.2010.12.005

Cite this

Moreno-De-Luca, D., Mulle, J. G., Kaminsky, E. B., Sanders, S. J., Myers, S. M., Adam, M. P., Pakula, A. T., Eisenhauer, N. J., Uhas, K., Weik, L., Guy, L., Care, M. E., Morel, C. F., Boni, C., Salbert, B. A., Chandrareddy, A., Demmer, L. A., Chow, E. W. C., Surti, U., ... Ledbetter, D. H. (2011). Erratum: Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630)). American Journal of Human Genetics, 88(1), 121. https://doi.org/10.1016/j.ajhg.2010.12.005

Erratum: Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630)). / Moreno-De-Luca, Daniel; Mulle, Jennifer G.; Kaminsky, Erin B. et al.
In: American Journal of Human Genetics, Vol. 88, No. 1, 07.01.2011, p. 121.

Research output: Contribution to journal › Comment/debate › peer-review

Moreno-De-Luca, D, Mulle, JG, Kaminsky, EB, Sanders, SJ, Myers, SM, Adam, MP, Pakula, AT, Eisenhauer, NJ, Uhas, K, Weik, L, Guy, L, Care, ME, Morel, CF, Boni, C, Salbert, BA, Chandrareddy, A, Demmer, LA, Chow, EWC, Surti, U, Aradhya, S, Pickering, DL, Golden, DM, Sanger, WG, Aston, E, Brothman, AR, Gliem, TJ, Thorland, EC, Ackley, T, Iyer, R, Huang, S, Barber, JC, Crolla, JA, Warren, ST, Martin, CL & Ledbetter, DH 2011, 'Erratum: Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630))', American Journal of Human Genetics, vol. 88, no. 1, pp. 121. https://doi.org/10.1016/j.ajhg.2010.12.005

@article{d7c6d2e192d6468c9453b1d958aa8fd9,

title = "Erratum: Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630))",

author = "Daniel Moreno-De-Luca and Mulle, {Jennifer G.} and Kaminsky, {Erin B.} and Sanders, {Stephan J.} and Myers, {Scott M.} and Adam, {Margaret P.} and Pakula, {Amy T.} and Eisenhauer, {Nancy J.} and Kim Uhas and Luann Weik and Lisa Guy and Care, {Melanie E.} and Morel, {Chantal F.} and Charlotte Boni and Salbert, {Bonnie Anne} and Ashadeep Chandrareddy and Demmer, {Laurie A.} and Chow, {Eva W.C.} and Urvashi Surti and Swaroop Aradhya and Pickering, {Diane L.} and Golden, {Denae M.} and Sanger, {Warren G.} and Emily Aston and Brothman, {Arthur R.} and Gliem, {Troy J.} and Thorland, {Erik C.} and Todd Ackley and Ram Iyer and Shuwen Huang and Barber, {John C.} and Crolla, {John A.} and Warren, {Stephen T.} and Martin, {Christa L.} and Ledbetter, {David H.}",

note = "Funding Information: This work was funded in part by NIH grants MH074090 (D.H.L. and C.L.M.), HD064525 (D.H.L. and C.L.M.), MH081754 (CLM), MH080583 (J.G.M.), MH080129 (S.T.W.), and MH071425 (K. Stefansson).",

year = "2011",

month = jan,

day = "7",

doi = "10.1016/j.ajhg.2010.12.005",

language = "English (US)",

volume = "88",

pages = "121",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "1",

}

TY - JOUR

T1 - Erratum

T2 - Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630))

AU - Moreno-De-Luca, Daniel

AU - Mulle, Jennifer G.

AU - Kaminsky, Erin B.

AU - Sanders, Stephan J.

AU - Myers, Scott M.

AU - Adam, Margaret P.

AU - Pakula, Amy T.

AU - Eisenhauer, Nancy J.

AU - Uhas, Kim

AU - Weik, Luann

AU - Guy, Lisa

AU - Care, Melanie E.

AU - Morel, Chantal F.

AU - Boni, Charlotte

AU - Salbert, Bonnie Anne

AU - Chandrareddy, Ashadeep

AU - Demmer, Laurie A.

AU - Chow, Eva W.C.

AU - Surti, Urvashi

AU - Aradhya, Swaroop

AU - Pickering, Diane L.

AU - Golden, Denae M.

AU - Sanger, Warren G.

AU - Aston, Emily

AU - Brothman, Arthur R.

AU - Gliem, Troy J.

AU - Thorland, Erik C.

AU - Ackley, Todd

AU - Iyer, Ram

AU - Huang, Shuwen

AU - Barber, John C.

AU - Crolla, John A.

AU - Warren, Stephen T.

AU - Martin, Christa L.

AU - Ledbetter, David H.

N1 - Funding Information: This work was funded in part by NIH grants MH074090 (D.H.L. and C.L.M.), HD064525 (D.H.L. and C.L.M.), MH081754 (CLM), MH080583 (J.G.M.), MH080129 (S.T.W.), and MH071425 (K. Stefansson).

PY - 2011/1/7

Y1 - 2011/1/7

UR - http://www.scopus.com/inward/record.url?scp=78650895861&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=78650895861&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2010.12.005

DO - 10.1016/j.ajhg.2010.12.005

M3 - Comment/debate

AN - SCOPUS:78650895861

SN - 0002-9297

VL - 88

SP - 121

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 1

ER -

Erratum: Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630))

ASJC Scopus subject areas

Access to Document

Other files and links

Cite this