Individual common variants exert weak effects on the risk for autism spectrum disorders.

Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, Corsello C, Crawford EL, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Gilbert J, Gillberg C, Glessner JT, Green A, Green J, Guter SJ, Heron EA, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Jacob S, Kenny GP, Kim C, Kolevzon A, Kustanovich V, Lajonchere CM, Lamb JA, Law-Smith M, Leboyer M, Le Couteur A, Leventhal BL, Liu XQ, Lombard F, Lord C, Lotspeich L, Lund SC, Magalhaes TR, Mantoulan C, McDougle CJ, Melhem NM, Merikangas A, Minshew NJ, Mirza GK, Munson J, Noakes C, Nygren G, Papanikolaou K, Pagnamenta AT, Parrini B, Paton T, Pickles A, Posey DJ, Poustka F, Ragoussis J, Regan R, Roberts W, Roeder K, Roge B, Rutter ML, Schlitt S, Shah N, Sheffield VC, Soorya L, Sousa I, Stoppioni V, Sykes N, Tancredi R, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Vorstman JA, Wallace S, Wing K, Wittemeyer K, Wood S, Zurawiecki D, Zwaigenbaum L, Bailey AJ, Battaglia A, Cantor RM, Coon H, Cuccaro ML, Dawson G, Ennis S, Freitag CM, Geschwind DH, Haines JL, Klauck SM, McMahon WM, Maestrini E, Miller J, Monaco AP, Nelson SF, Nurnberger JI Jr, Oliveira G, Parr JR, Pericak-Vance MA, Piven J, Schellenberg GD, Scherer SW, Vicente AM, Wassink TH, Wijsman EM, Betancur C, Buxbaum JD, Cook EH, Gallagher L, Gill M, Hallmayer J, Paterson AD, Sutcliffe JS, Szatmari P, Vieland VJ, Hakonarson H, Devlin B

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DOI: 10.1093/hmg/dds301
Published: 2012 Nov 1
Container: Human molecular genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1093/hmg/dds301,
  title = {Individual common variants exert weak effects on the risk for autism spectrum disorders.},
  author = {Anney R and Klei L and Pinto D and Almeida J and Bacchelli E and Baird G and Bolshakova N and Bölte S and Bolton PF and Bourgeron T and Brennan S and Brian J and Casey J and Conroy J and Correia C and Corsello C and Crawford EL and de Jonge M and Delorme R and Duketis E and Duque F and Estes A and Farrar P and Fernandez BA and Folstein SE and Fombonne E and Gilbert J and Gillberg C and Glessner JT and Green A and Green J and Guter SJ and Heron EA and Holt R and Howe JL and Hughes G and Hus V and Igliozzi R and Jacob S and Kenny GP and Kim C and Kolevzon A and Kustanovich V and Lajonchere CM and Lamb JA and Law-Smith M and Leboyer M and Le Couteur A and Leventhal BL and Liu XQ and Lombard F and Lord C and Lotspeich L and Lund SC and Magalhaes TR and Mantoulan C and McDougle CJ and Melhem NM and Merikangas A and Minshew NJ and Mirza GK and Munson J and Noakes C and Nygren G and Papanikolaou K and Pagnamenta AT and Parrini B and Paton T and Pickles A and Posey DJ and Poustka F and Ragoussis J and Regan R and Roberts W and Roeder K and Roge B and Rutter ML and Schlitt S and Shah N and Sheffield VC and Soorya L and Sousa I and Stoppioni V and Sykes N and Tancredi R and Thompson AP and Thomson S and Tryfon A and Tsiantis J and Van Engeland H and Vincent JB and Volkmar F and Vorstman JA and Wallace S and Wing K and Wittemeyer K and Wood S and Zurawiecki D and Zwaigenbaum L and Bailey AJ and Battaglia A and Cantor RM and Coon H and Cuccaro ML and Dawson G and Ennis S and Freitag CM and Geschwind DH and Haines JL and Klauck SM and McMahon WM and Maestrini E and Miller J and Monaco AP and Nelson SF and Nurnberger JI Jr and Oliveira G and Parr JR and Pericak-Vance MA and Piven J and Schellenberg GD and Scherer SW and Vicente AM and Wassink TH and Wijsman EM and Betancur C and Buxbaum JD and Cook EH and Gallagher L and Gill M and Hallmayer J and Paterson AD and Sutcliffe JS and Szatmari P and Vieland VJ and Hakonarson H and Devlin B},
  year = {2012},
  journal = {Human molecular genetics},
  doi = {10.1093/hmg/dds301},
  url = {https://doi.org/10.1093/hmg/dds301}
}

RIS

TY  - JOUR
TI  - Individual common variants exert weak effects on the risk for autism spectrum disorders.
AU  - Anney R
AU  - Klei L
AU  - Pinto D
AU  - Almeida J
AU  - Bacchelli E
AU  - Baird G
AU  - Bolshakova N
AU  - Bölte S
AU  - Bolton PF
AU  - Bourgeron T
AU  - Brennan S
AU  - Brian J
AU  - Casey J
AU  - Conroy J
AU  - Correia C
AU  - Corsello C
AU  - Crawford EL
AU  - de Jonge M
AU  - Delorme R
AU  - Duketis E
AU  - Duque F
AU  - Estes A
AU  - Farrar P
AU  - Fernandez BA
AU  - Folstein SE
AU  - Fombonne E
AU  - Gilbert J
AU  - Gillberg C
AU  - Glessner JT
AU  - Green A
AU  - Green J
AU  - Guter SJ
AU  - Heron EA
AU  - Holt R
AU  - Howe JL
AU  - Hughes G
AU  - Hus V
AU  - Igliozzi R
AU  - Jacob S
AU  - Kenny GP
AU  - Kim C
AU  - Kolevzon A
AU  - Kustanovich V
AU  - Lajonchere CM
AU  - Lamb JA
AU  - Law-Smith M
AU  - Leboyer M
AU  - Le Couteur A
AU  - Leventhal BL
AU  - Liu XQ
AU  - Lombard F
AU  - Lord C
AU  - Lotspeich L
AU  - Lund SC
AU  - Magalhaes TR
AU  - Mantoulan C
AU  - McDougle CJ
AU  - Melhem NM
AU  - Merikangas A
AU  - Minshew NJ
AU  - Mirza GK
AU  - Munson J
AU  - Noakes C
AU  - Nygren G
AU  - Papanikolaou K
AU  - Pagnamenta AT
AU  - Parrini B
AU  - Paton T
AU  - Pickles A
AU  - Posey DJ
AU  - Poustka F
AU  - Ragoussis J
AU  - Regan R
AU  - Roberts W
AU  - Roeder K
AU  - Roge B
AU  - Rutter ML
AU  - Schlitt S
AU  - Shah N
AU  - Sheffield VC
AU  - Soorya L
AU  - Sousa I
AU  - Stoppioni V
AU  - Sykes N
AU  - Tancredi R
AU  - Thompson AP
AU  - Thomson S
AU  - Tryfon A
AU  - Tsiantis J
AU  - Van Engeland H
AU  - Vincent JB
AU  - Volkmar F
AU  - Vorstman JA
AU  - Wallace S
AU  - Wing K
AU  - Wittemeyer K
AU  - Wood S
AU  - Zurawiecki D
AU  - Zwaigenbaum L
AU  - Bailey AJ
AU  - Battaglia A
AU  - Cantor RM
AU  - Coon H
AU  - Cuccaro ML
AU  - Dawson G
AU  - Ennis S
AU  - Freitag CM
AU  - Geschwind DH
AU  - Haines JL
AU  - Klauck SM
AU  - McMahon WM
AU  - Maestrini E
AU  - Miller J
AU  - Monaco AP
AU  - Nelson SF
AU  - Nurnberger JI Jr
AU  - Oliveira G
AU  - Parr JR
AU  - Pericak-Vance MA
AU  - Piven J
AU  - Schellenberg GD
AU  - Scherer SW
AU  - Vicente AM
AU  - Wassink TH
AU  - Wijsman EM
AU  - Betancur C
AU  - Buxbaum JD
AU  - Cook EH
AU  - Gallagher L
AU  - Gill M
AU  - Hallmayer J
AU  - Paterson AD
AU  - Sutcliffe JS
AU  - Szatmari P
AU  - Vieland VJ
AU  - Hakonarson H
AU  - Devlin B
PY  - 2012
JO  - Human molecular genetics
DO  - 10.1093/hmg/dds301
UR  - https://doi.org/10.1093/hmg/dds301
ER  -

APA

R, A., L, K., D, P., J, A., E, B., G, B., N, B., S, B., PF, B., T, B., S, B., J, B., J, C., J, C., C, C., C, C., EL, C., M, D. J., R, D., E, D., F, D., A, E., P, F., BA, F., SE, F., E, F., J, G., C, G., JT, G., A, G., J, G., SJ, G., EA, H., R, H., JL, H., G, H., V, H., R, I., S, J., GP, K., C, K., A, K., V, K., CM, L., JA, L., M, L., M, L., A, L. C., BL, L., XQ, L., F, L., C, L., L, L., SC, L., TR, M., C, M., CJ, M., NM, M., A, M., NJ, M., GK, M., J, M., C, N., G, N., K, P., AT, P., B, P., T, P., A, P., DJ, P., F, P., J, R., R, R., W, R., K, R., B, R., ML, R., S, S., N, S., VC, S., L, S., I, S., V, S., N, S., R, T., AP, T., S, T., A, T., J, T., H, V. E., JB, V., F, V., JA, V., S, W., K, W., K, W., S, W., D, Z., L, Z., AJ, B., A, B., RM, C., H, C., ML, C., G, D., S, E., CM, F., DH, G., JL, H., SM, K., WM, M., E, M., J, M., AP, M., SF, N., Jr, N. J., G, O., JR, P., MA, P., J, P., GD, S., SW, S., AM, V., TH, W., EM, W., C, B., JD, B., EH, C., L, G., M, G., J, H., AD, P., JS, S., P, S., VJ, V., H, H., & B, D. (2012). Individual common variants exert weak effects on the risk for autism spectrum disorders.. Human molecular genetics. https://doi.org/10.1093/hmg/dds301

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pubmed · retrieved 2026-09-25T02:06:05.831Z