A genome-wide scan for common alleles affecting risk for autism

R. Anney, L. Klei, D. Pinto, R. Regan, J. Conroy, T. R. Magalhaes, C. Correia, B. S. Abrahams, N. Sykes, A. T. Pagnamenta, J. Almeida, E. Bacchelli, A. J. Bailey, G. Baird, A. Battaglia, T. Berney, N. Bolshakova, S. Bolte, P. F. Bolton, T. Bourgeron, S. Brennan, J. Brian, A. R. Carson, G. Casallo, J. Casey, S. H. Chu, L. Cochrane, C. Corsello, E. L. Crawford, A. Crossett, G. Dawson, M. de Jonge, R. Delorme, I. Drmic, E. Duketis, F. Duque, A. Estes, P. Farrar, B. A. Fernandez, S. E. Folstein, E. Fombonne, C. M. Freitag, J. Gilbert, C. Gillberg, J. T. Glessner, J. Goldberg, J. Green, S. J. Guter, H. Hakonarson, E. A. Heron, M. Hill, R. Holt, J. L. Howe, G. Hughes, V. Hus, R. Igliozzi, C. Kim, S. M. Klauck, A. Kolevzon, O. Korvatska, V. Kustanovich, C. M. Lajonchere, J. A. Lamb, M. Laskawiec, M. Leboyer, A. Le Couteur, B. L. Leventhal, A. C. Lionel, X.-Q. Liu, C. Lord, L. Lotspeich, S. C. Lund, E. Maestrini, W. Mahoney, C. Mantoulan, C. R. Marshall, H. McConachie, C. J. McDougle, J. McGrath, W. M. McMahon, N. M. Melhem, A. Merikangas, O. Migita, N. J. Minshew, G. K. Mirza, J. Munson, S. F. Nelson, C. Noakes, A. Noor, G. Nygren, G. Oliveira, K. Papanikolaou, J. R. Parr, B. Parrini, T. Paton, A. Pickles, J. Piven, D. J. Posey, A. Poustka, F. Poustka, A. Prasad, J. Ragoussis, K. Renshaw, J. Rickaby, W. Roberts, K. Roeder, B. Roge, M. L. Rutter, L. J. Bierut, J. P. Rice, J. Salt, K. Sansom, D. Sato, R. Segurado, L. Senman, N. Shah, V. C. Sheffield, L. Soorya, I. Sousa, V. Stoppioni, C. Strawbridge, R. Tancredi, K. Tansey, B. Thiruvahindrapduram, A. P. Thompson, S. Thomson, A. Tryfon, J. Tsiantis, H. Van Engeland, J. B. Vincent, F. Volkmar, S. Wallace, K. Wang, Z. Wang, T. H. Wassink, K. Wing, K. Wittemeyer, S. Wood, B. L. Yaspan, D. Zurawiecki, L. Zwaigenbaum, C. Betancur, J. D. Buxbaum, R. M. Cantor, E. H. Cook, H. Coon, M. L. Cuccaro, L. Gallagher, D. H. Geschwind, M. Gill, J. L. Haines, J. Miller, A. P. Monaco, J. I. Nurnberger, A. D. Paterson, M. A. Pericak-Vance, G. D. Schellenberg, S. W. Scherer, J. S. Sutcliffe, P. Szatmari, A. M. Vicente, V. J. Vieland, E. M. Wijsman, B. Devlin, S. Ennis, J. Hallmayer

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DOI: 10.1093/hmg/ddq307
Published: 2010-07-27
Container: Human Molecular Genetics
Publisher: Oxford University Press (OUP)
Open access: unknown

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BibTeX

@article{allodium:10.1093/hmg/ddq307,
title = {A genome-wide scan for common alleles affecting risk for autism},
author = {R. Anney and L. Klei and D. Pinto and R. Regan and J. Conroy and T. R. Magalhaes and C. Correia and B. S. Abrahams and N. Sykes and A. T. Pagnamenta and J. Almeida and E. Bacchelli and A. J. Bailey and G. Baird and A. Battaglia and T. Berney and N. Bolshakova and S. Bolte and P. F. Bolton and T. Bourgeron and S. Brennan and J. Brian and A. R. Carson and G. Casallo and J. Casey and S. H. Chu and L. Cochrane and C. Corsello and E. L. Crawford and A. Crossett and G. Dawson and M. de Jonge and R. Delorme and I. Drmic and E. Duketis and F. Duque and A. Estes and P. Farrar and B. A. Fernandez and S. E. Folstein and E. Fombonne and C. M. Freitag and J. Gilbert and C. Gillberg and J. T. Glessner and J. Goldberg and J. Green and S. J. Guter and H. Hakonarson and E. A. Heron and M. Hill and R. Holt and J. L. Howe and G. Hughes and V. Hus and R. Igliozzi and C. Kim and S. M. Klauck and A. Kolevzon and O. Korvatska and V. Kustanovich and C. M. Lajonchere and J. A. Lamb and M. Laskawiec and M. Leboyer and A. Le Couteur and B. L. Leventhal and A. C. Lionel and X.-Q. Liu and C. Lord and L. Lotspeich and S. C. Lund and E. Maestrini and W. Mahoney and C. Mantoulan and C. R. Marshall and H. McConachie and C. J. McDougle and J. McGrath and W. M. McMahon and N. M. Melhem and A. Merikangas and O. Migita and N. J. Minshew and G. K. Mirza and J. Munson and S. F. Nelson and C. Noakes and A. Noor and G. Nygren and G. Oliveira and K. Papanikolaou and J. R. Parr and B. Parrini and T. Paton and A. Pickles and J. Piven and D. J. Posey and A. Poustka and F. Poustka and A. Prasad and J. Ragoussis and K. Renshaw and J. Rickaby and W. Roberts and K. Roeder and B. Roge and M. L. Rutter and L. J. Bierut and J. P. Rice and J. Salt and K. Sansom and D. Sato and R. Segurado and L. Senman and N. Shah and V. C. Sheffield and L. Soorya and I. Sousa and V. Stoppioni and C. Strawbridge and R. Tancredi and K. Tansey and B. Thiruvahindrapduram and A. P. Thompson and S. Thomson and A. Tryfon and J. Tsiantis and H. Van Engeland and J. B. Vincent and F. Volkmar and S. Wallace and K. Wang and Z. Wang and T. H. Wassink and K. Wing and K. Wittemeyer and S. Wood and B. L. Yaspan and D. Zurawiecki and L. Zwaigenbaum and C. Betancur and J. D. Buxbaum and R. M. Cantor and E. H. Cook and H. Coon and M. L. Cuccaro and L. Gallagher and D. H. Geschwind and M. Gill and J. L. Haines and J. Miller and A. P. Monaco and J. I. Nurnberger and A. D. Paterson and M. A. Pericak-Vance and G. D. Schellenberg and S. W. Scherer and J. S. Sutcliffe and P. Szatmari and A. M. Vicente and V. J. Vieland and E. M. Wijsman and B. Devlin and S. Ennis and J. Hallmayer},
year = {2010},
journal = {Human Molecular Genetics},
doi = {10.1093/hmg/ddq307},
url = {https://doi.org/10.1093/hmg/ddq307}
}

RIS

TY  - JOUR
TI  - A genome-wide scan for common alleles affecting risk for autism
AU  - R. Anney
AU  - L. Klei
AU  - D. Pinto
AU  - R. Regan
AU  - J. Conroy
AU  - T. R. Magalhaes
AU  - C. Correia
AU  - B. S. Abrahams
AU  - N. Sykes
AU  - A. T. Pagnamenta
AU  - J. Almeida
AU  - E. Bacchelli
AU  - A. J. Bailey
AU  - G. Baird
AU  - A. Battaglia
AU  - T. Berney
AU  - N. Bolshakova
AU  - S. Bolte
AU  - P. F. Bolton
AU  - T. Bourgeron
AU  - S. Brennan
AU  - J. Brian
AU  - A. R. Carson
AU  - G. Casallo
AU  - J. Casey
AU  - S. H. Chu
AU  - L. Cochrane
AU  - C. Corsello
AU  - E. L. Crawford
AU  - A. Crossett
AU  - G. Dawson
AU  - M. de Jonge
AU  - R. Delorme
AU  - I. Drmic
AU  - E. Duketis
AU  - F. Duque
AU  - A. Estes
AU  - P. Farrar
AU  - B. A. Fernandez
AU  - S. E. Folstein
AU  - E. Fombonne
AU  - C. M. Freitag
AU  - J. Gilbert
AU  - C. Gillberg
AU  - J. T. Glessner
AU  - J. Goldberg
AU  - J. Green
AU  - S. J. Guter
AU  - H. Hakonarson
AU  - E. A. Heron
AU  - M. Hill
AU  - R. Holt
AU  - J. L. Howe
AU  - G. Hughes
AU  - V. Hus
AU  - R. Igliozzi
AU  - C. Kim
AU  - S. M. Klauck
AU  - A. Kolevzon
AU  - O. Korvatska
AU  - V. Kustanovich
AU  - C. M. Lajonchere
AU  - J. A. Lamb
AU  - M. Laskawiec
AU  - M. Leboyer
AU  - A. Le Couteur
AU  - B. L. Leventhal
AU  - A. C. Lionel
AU  - X.-Q. Liu
AU  - C. Lord
AU  - L. Lotspeich
AU  - S. C. Lund
AU  - E. Maestrini
AU  - W. Mahoney
AU  - C. Mantoulan
AU  - C. R. Marshall
AU  - H. McConachie
AU  - C. J. McDougle
AU  - J. McGrath
AU  - W. M. McMahon
AU  - N. M. Melhem
AU  - A. Merikangas
AU  - O. Migita
AU  - N. J. Minshew
AU  - G. K. Mirza
AU  - J. Munson
AU  - S. F. Nelson
AU  - C. Noakes
AU  - A. Noor
AU  - G. Nygren
AU  - G. Oliveira
AU  - K. Papanikolaou
AU  - J. R. Parr
AU  - B. Parrini
AU  - T. Paton
AU  - A. Pickles
AU  - J. Piven
AU  - D. J. Posey
AU  - A. Poustka
AU  - F. Poustka
AU  - A. Prasad
AU  - J. Ragoussis
AU  - K. Renshaw
AU  - J. Rickaby
AU  - W. Roberts
AU  - K. Roeder
AU  - B. Roge
AU  - M. L. Rutter
AU  - L. J. Bierut
AU  - J. P. Rice
AU  - J. Salt
AU  - K. Sansom
AU  - D. Sato
AU  - R. Segurado
AU  - L. Senman
AU  - N. Shah
AU  - V. C. Sheffield
AU  - L. Soorya
AU  - I. Sousa
AU  - V. Stoppioni
AU  - C. Strawbridge
AU  - R. Tancredi
AU  - K. Tansey
AU  - B. Thiruvahindrapduram
AU  - A. P. Thompson
AU  - S. Thomson
AU  - A. Tryfon
AU  - J. Tsiantis
AU  - H. Van Engeland
AU  - J. B. Vincent
AU  - F. Volkmar
AU  - S. Wallace
AU  - K. Wang
AU  - Z. Wang
AU  - T. H. Wassink
AU  - K. Wing
AU  - K. Wittemeyer
AU  - S. Wood
AU  - B. L. Yaspan
AU  - D. Zurawiecki
AU  - L. Zwaigenbaum
AU  - C. Betancur
AU  - J. D. Buxbaum
AU  - R. M. Cantor
AU  - E. H. Cook
AU  - H. Coon
AU  - M. L. Cuccaro
AU  - L. Gallagher
AU  - D. H. Geschwind
AU  - M. Gill
AU  - J. L. Haines
AU  - J. Miller
AU  - A. P. Monaco
AU  - J. I. Nurnberger
AU  - A. D. Paterson
AU  - M. A. Pericak-Vance
AU  - G. D. Schellenberg
AU  - S. W. Scherer
AU  - J. S. Sutcliffe
AU  - P. Szatmari
AU  - A. M. Vicente
AU  - V. J. Vieland
AU  - E. M. Wijsman
AU  - B. Devlin
AU  - S. Ennis
AU  - J. Hallmayer
PY  - 2010
JO  - Human Molecular Genetics
DO  - 10.1093/hmg/ddq307
UR  - https://doi.org/10.1093/hmg/ddq307
ER  -

APA

Anney, R., Klei, L., Pinto, D., Regan, R., Conroy, J., Magalhaes, T. R., Correia, C., Abrahams, B. S., Sykes, N., Pagnamenta, A. T., Almeida, J., Bacchelli, E., Bailey, A. J., Baird, G., Battaglia, A., Berney, T., Bolshakova, N., Bolte, S., Bolton, P. F., Bourgeron, T., Brennan, S., Brian, J., Carson, A. R., Casallo, G., Casey, J., Chu, S. H., Cochrane, L., Corsello, C., Crawford, E. L., Crossett, A., Dawson, G., Jonge, M. D., Delorme, R., Drmic, I., Duketis, E., Duque, F., Estes, A., Farrar, P., Fernandez, B. A., Folstein, S. E., Fombonne, E., Freitag, C. M., Gilbert, J., Gillberg, C., Glessner, J. T., Goldberg, J., Green, J., Guter, S. J., Hakonarson, H., Heron, E. A., Hill, M., Holt, R., Howe, J. L., Hughes, G., Hus, V., Igliozzi, R., Kim, C., Klauck, S. M., Kolevzon, A., Korvatska, O., Kustanovich, V., Lajonchere, C. M., Lamb, J. A., Laskawiec, M., Leboyer, M., Couteur, A. L., Leventhal, B. L., Lionel, A. C., Liu, X., Lord, C., Lotspeich, L., Lund, S. C., Maestrini, E., Mahoney, W., Mantoulan, C., Marshall, C. R., McConachie, H., McDougle, C. J., McGrath, J., McMahon, W. M., Melhem, N. M., Merikangas, A., Migita, O., Minshew, N. J., Mirza, G. K., Munson, J., Nelson, S. F., Noakes, C., Noor, A., Nygren, G., Oliveira, G., Papanikolaou, K., Parr, J. R., Parrini, B., Paton, T., Pickles, A., Piven, J., Posey, D. J., Poustka, A., Poustka, F., Prasad, A., Ragoussis, J., Renshaw, K., Rickaby, J., Roberts, W., Roeder, K., Roge, B., Rutter, M. L., Bierut, L. J., Rice, J. P., Salt, J., Sansom, K., Sato, D., Segurado, R., Senman, L., Shah, N., Sheffield, V. C., Soorya, L., Sousa, I., Stoppioni, V., Strawbridge, C., Tancredi, R., Tansey, K., Thiruvahindrapduram, B., Thompson, A. P., Thomson, S., Tryfon, A., Tsiantis, J., Engeland, H. V., Vincent, J. B., Volkmar, F., Wallace, S., Wang, K., Wang, Z., Wassink, T. H., Wing, K., Wittemeyer, K., Wood, S., Yaspan, B. L., Zurawiecki, D., Zwaigenbaum, L., Betancur, C., Buxbaum, J. D., Cantor, R. M., Cook, E. H., Coon, H., Cuccaro, M. L., Gallagher, L., Geschwind, D. H., Gill, M., Haines, J. L., Miller, J., Monaco, A. P., Nurnberger, J. I., Paterson, A. D., Pericak-Vance, M. A., Schellenberg, G. D., Scherer, S. W., Sutcliffe, J. S., Szatmari, P., Vicente, A. M., Vieland, V. J., Wijsman, E. M., Devlin, B., Ennis, S., & Hallmayer, J. (2010). A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. https://doi.org/10.1093/hmg/ddq307

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