BetterScholar BetterScholar
12
Role
Title
Level Year L/R
🐜 Functional impact of global rare copy number variation in autism spectrum disorders
176 auth. D. Pinto, A. Pagnamenta, L. Klei, R. Anney, D. Merico, R. Regan, J. Conroy, T. Magalhães, C. Correia, B. Abrahams, J. Almeida, E. Bacchelli, Gary D Bader, A. Bailey, G. Baird, ... A. Battaglia, T. Berney, N. Bolshakova, S. Bölte, P. Bolton, T. Bourgeron, Sean Brennan, J. Brian, S. Bryson, A. Carson, G. Casallo, J. Casey, B. Chung, L. Cochrane, Christina M. Corsello, Emily L. Crawford, Andrew Crossett, C. Cytrynbaum, G. Dawson, M. Jonge, R. Delorme, Irene Drmic, E. Duketis, F. Duque, A. Estes, Penny Farrar, B. Fernandez, S. Folstein, E. Fombonne, C. Freitag, J. Gilbert, C. Gillberg, J. Glessner, J. Goldberg, A. Green, Jonathan Green, Stephen J. Guter, H. Hakonarson, E. Heron, M. Hill, R. Holt, J. Howe, G. Hughes, Vanessa Hus, R. Igliozzi, Cecilia Kim, S. Klauck, A. Kolevzon, Olena Korvatska, Vlad Kustanovich, C. Lajonchere, J. Lamb, Magdalena Laskawiec, M. Leboyer, A. Couteur, B. Leventhal, A. C. Lionel, Xiao-qing Liu, C. Lord, L. Lotspeich, Sabata C. Lund, E. Maestrini, W. Mahoney, Carine Mantoulan, C. Marshall, H. McConachie, C. McDougle, J. McGrath, W. McMahon, Alison K. Merikangas, O. Migita, N. Minshew, G. Mirza, J. Munson, S. Nelson, Carolyn Noakes, A. Noor, G. Nygren, G. Oliveira, K. Papanikolaou, J. Parr, B. Parrini, T. Paton, A. Pickles, M. Pilorge, J. Piven, C. Ponting, D. Posey, A. Poustka, F. Poustka, Aparna Prasad, J. Ragoussis, Katy Renshaw, Jessica Rickaby, W. Roberts, K. Roeder, B. Rogé, M. Rutter, L. Bierut, J. Rice, Jeff Salt, K. Sansom, Daisuke Sato, R. Segurado, A. Sequeira, Lili Senman, N. Shah, V. Sheffield, L. Soorya, I. Sousa, O. Stein, N. Sykes, Vera Stoppioni, Christina P Strawbridge, R. Tancredi, K. Tansey, Bhooma Thiruvahindrapduram, A. Thompson, Susanne A. Thomson, A. Tryfon, J. Tsiantis, H. Engeland, J. Vincent, F. Volkmar, S. Wallace, Kai Wang, Zhouzhi Wang, T. Wassink, C. Webber, R. Weksberg, Kirsty Wing, Kerstin Wittemeyer, Shawn Wood, B. Yaspan, Danielle M Zurawiecki, L. Zwaigenbaum, J. Buxbaum, R. Cantor, E. Cook, H. Coon, M. Cuccaro, B. Devlin, S. Ennis, L. Gallagher, D. Geschwind, M. Gill, J. Haines, Joachim Hallmayer, Judith S Miller, A. Monaco, J. Nurnberger, A. Paterson, M. Pericak-Vance, G. Schellenberg, P. Szatmari, A. Vicente, V. Vieland, E. Wijsman, S. Scherer, J. Sutcliffe, C. Betancur
10 2010
10
🐜
🐜 Mapping autism risk loci using genetic linkage and chromosomal rearrangements
138 auth. P. Szatmari, A. Paterson, L. Zwaigenbaum, W. Roberts, J. Brian, Xiao-qing Liu, J. Vincent, J. Skaug, A. Thompson, Lili Senman, L. Feuk, Cheng Qian, S. Bryson, Marshall B. Jones, C. Marshall, ... S. Scherer, V. Vieland, Christopher Bartlett, L. Mangin, R. Goedken, Alberto Maria Segre, M. Pericak-Vance, M. Cuccaro, J. Gilbert, H. Wright, R. Abramson, C. Betancur, T. Bourgeron, C. Gillberg, M. Leboyer, J. Buxbaum, K. Davis, E. Hollander, J. Silverman, Joachim Hallmayer, L. Lotspeich, J. Sutcliffe, J. Haines, S. Folstein, J. Piven, T. Wassink, V. Sheffield, D. Geschwind, M. Bucan, W. Brown, R. Cantor, J. Constantino, T. Gilliam, M. Herbert, C. Lajonchere, D. Ledbetter, Christa Lese-Martin, Janet Miller, S. Nelson, C. Samango-Sprouse, S. Spence, M. State, R. Tanzi, H. Coon, G. Dawson, B. Devlin, A. Estes, P. Flodman, L. Klei, W. McMahon, N. Minshew, J. Munson, E. Korvatska, P. Rodier, G. Schellenberg, Moyra J. Smith, M. Spence, C. Stodgell, P. Tepper, E. Wijsman, Chang-En Yu, B. Rogé, Carine Mantoulan, Kerstin Wittemeyer, A. Poustka, B. Felder, S. Klauck, C. Schuster, F. Poustka, S. Bölte, Sabine Feineis-Matthews, Evelyn Herbrecht, G. Schmötzer, J. Tsiantis, K. Papanikolaou, E. Maestrini, E. Bacchelli, F. Blasi, Simona Carone, Claudio Toma, H. van Engeland, M. D. de Jonge, C. Kemner, F. Koop, M. Langemeijer, Channa T. Hijmans, W. Staal, G. Baird, P. Bolton, M. Rutter, E. Weisblatt, Jonathan Green, C. Aldred, J. Wilkinson, A. Pickles, A. Le Couteur, T. Berney, H. McConachie, A. Bailey, Kostas Francis, Gemma Honeyman, A. Hutchinson, J. Parr, S. Wallace, A. Monaco, G. Barnby, Kazuhiro Kobayashi, J. Lamb, I. Sousa, N. Sykes, E. Cook, Stephen J. Guter, B. Leventhal, Jeff Salt, C. Lord, Christina M. Corsello, Vanessa Hus, D. Weeks, F. Volkmar, M. Tauber, E. Fombonne, A. Shih, Kacie J. Meyer
10 2007
10
🐜
🐜 A genome-wide scan for common alleles affecting risk for autism
166 auth. R. Anney, L. Klei, D. Pinto, R. Regan, J. Conroy, T. Magalhães, C. Correia, B. Abrahams, N. Sykes, A. Pagnamenta, J. Almeida, E. Bacchelli, A. Bailey, G. Baird, A. Battaglia, ... T. Berney, N. Bolshakova, S. Bölte, P. Bolton, T. Bourgeron, Sean Brennan, J. Brian, A. Carson, G. Casallo, J. Casey, S. Chu, L. Cochrane, Christina M. Corsello, Emily L. Crawford, Andrew Crossett, G. Dawson, M. D. de Jonge, R. Delorme, Irene Drmic, E. Duketis, F. Duque, A. Estes, Penny Farrar, B. Fernandez, S. Folstein, E. Fombonne, C. Freitag, J. Gilbert, C. Gillberg, J. Glessner, J. Goldberg, Jonathan Green, Stephen J. Guter, H. Hakonarson, E. Heron, M. Hill, R. Holt, J. Howe, G. Hughes, Vanessa Hus, R. Igliozzi, Cecilia Kim, S. Klauck, A. Kolevzon, Olena Korvatska, Vlad Kustanovich, C. Lajonchere, J. Lamb, Magdalena Laskawiec, M. Leboyer, A. Le Couteur, B. Leventhal, A. C. Lionel, Xiao-qing Liu, C. Lord, L. Lotspeich, Sabata C. Lund, E. Maestrini, W. Mahoney, Carine Mantoulan, C. Marshall, H. McConachie, C. McDougle, J. McGrath, W. McMahon, N. Melhem, Alison K. Merikangas, O. Migita, N. Minshew, G. Mirza, J. Munson, S. Nelson, Carolyn Noakes, A. Noor, G. Nygren, G. Oliveira, K. Papanikolaou, J. Parr, B. Parrini, T. Paton, A. Pickles, J. Piven, D. Posey, A. Poustka, F. Poustka, Aparna Prasad, J. Ragoussis, Katy Renshaw, Jessica Rickaby, W. Roberts, K. Roeder, B. Rogé, M. Rutter, L. Bierut, J. Rice, Jeff Salt, K. Sansom, Daisuke Sato, R. Segurado, Lili Senman, N. Shah, V. Sheffield, L. Soorya, I. Sousa, Vera Stoppioni, Christina P Strawbridge, R. Tancredi, K. Tansey, Bhooma Thiruvahindrapduram, A. Thompson, Susanne A. Thomson, A. Tryfon, J. Tsiantis, H. van Engeland, J. Vincent, F. Volkmar, S. Wallace, Kai Wang, Zhouzhi Wang, T. Wassink, Kirsty Wing, Kerstin Wittemeyer, Shawn Wood, B. Yaspan, Danielle M Zurawiecki, L. Zwaigenbaum, C. Betancur, J. Buxbaum, R. Cantor, E. Cook, H. Coon, M. Cuccaro, L. Gallagher, D. Geschwind, M. Gill, J. Haines, Judith S Miller, A. Monaco, J. Nurnberger, A. Paterson, M. Pericak-Vance, G. Schellenberg, S. Scherer, J. Sutcliffe, P. Szatmari, A. Vicente, V. Vieland, E. Wijsman, B. Devlin, S. Ennis, Joachim Hallmayer
9 2010
9
🐜
🐜 A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.
64 auth. A. Bailey, A. Hervás, Nicola Matthews, S. Palferman, S. Wallace, Anne Aubin, J. Michelotti, Catherine Wainhouse, K. Papanikolaou, M. Rutter, E. Maestrini, A. Marlow, D. Weeks, J. Lamb, C. Francks, ... G. Kearsley, Pat Scudder, A. Monaco, G. Baird, A. Cox, H. Cockerill, Fleming Nuffield, A. Couteur, T. Berney, Hayley Cooper, T. Kelly, Jonathan Green, J. Whittaker, A. Gilchrist, P. Bolton, Anne Schönewald, M. Daker, C. Ogilvie, Z. Docherty, Z. Deans, Bryan D. Bolton, R. Packer, F. Poustka, D. Rühl, Gabriele Schmötzer, S. Bölte, S. Klauck, Anja Spieler, A. Poustka, H. Engeland, C. Kemner, M. Jonge, I. D. Hartog, C. Lord, E. Cook, B. Leventhal, F. Volkmar, D. Pauls, A. Klin, S. Smalley, E. Fombonne, B. Rogé, M. Tauber, E. Arti-Vartayan, Jeanne Fremolle-Kruck, L. Pederson, D. Haracopos, K. Brøndum‐Nielsen, R. Cotterill
9 1998
9
🐜
🐜 A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.
83 auth. S. Palferman, Nicola Matthews, M. Turner, Janette Moore, A. Hervás, Anne Aubin, S. Wallace, J. Michelotti, Catherine Wainhouse, A. Paul, E. Thompson, Ramyani P Gupta, C. Garner, Marianne Murin, C. Freitag, ... N. Ryder, E. Cottington, J. Parr, A. Pickles, M. Rutter, A. Bailey, G. Barnby, J. Lamb, A. Marlow, Pat Scudder, A. Monaco, G. Baird, A. Cox, Z. Docherty, P. Warburton, Elizabeth P. Green, S. Abbs, A. Couteur, H. McConachie, T. Berney, T. Kelly, P. D. Vries, P. Bolton, Jonathan Green, A. Gilchrist, J. Whittacker, Bryan D. Bolton, R. Packer, E. Maestrini, F. Blasi, H. Engeland, M. Jonge, C. Kemner, S. Klauck, K. S. Beyer, Sabine Epp, A. Poustka, A. Benner, Jw Goethe, F. Poustka, D. Rühl, Gabriele Schmötzer, S. Boolte, Sabine Feineis-Matthews, E. Fombonne, B. Rogee, Jeanne Fremolle-Kruck, C. Pienkowski, M. Tauber, Lennart Pedersen, Kb Nielsen, G. Eriksen, D. Haracopos, R. Cotterill, J. Tsiantis, K. Papanikolaou, C. Lord, Christina M. Corsello, Stephen J. Guter, B. Leventhal, E. Cook, S. Smalley, J. Bailey, J. McGough, J. Levitt, D. Pauls, F. Volkmar, D. Weeks
8 2001
8
🐜
🐜 Individual common variants exert weak effects on the risk for autism spectrum disorders
137 auth. R. Anney, L. Klei, D. Pinto, J. Almeida, E. Bacchelli, G. Baird, N. Bolshakova, S. Bölte, P. Bolton, T. Bourgeron, Sean Brennan, J. Brian, J. Casey, J. Conroy, C. Correia, ... Christina M. Corsello, Emily L. Crawford, M. D. de Jonge, R. Delorme, E. Duketis, F. Duque, A. Estes, Penny Farrar, B. Fernandez, S. Folstein, E. Fombonne, J. Gilbert, C. Gillberg, J. Glessner, A. Green, Jonathan Green, Stephen J. Guter, E. Heron, R. Holt, J. Howe, G. Hughes, Vanessa Hus, R. Igliozzi, Suma Jacob, G. Kenny, Cecilia Kim, A. Kolevzon, Vlad Kustanovich, C. Lajonchere, J. Lamb, Miriam Law-Smith, M. Leboyer, A. Le Couteur, B. Leventhal, Xiao-qing Liu, Frances Lombard, C. Lord, L. Lotspeich, Sabata C. Lund, T. Magalhães, Carine Mantoulan, C. McDougle, N. Melhem, Alison K. Merikangas, N. Minshew, G. Mirza, J. Munson, Carolyn Noakes, G. Nygren, K. Papanikolaou, A. Pagnamenta, B. Parrini, T. Paton, A. Pickles, D. Posey, F. Poustka, J. Ragoussis, R. Regan, W. Roberts, K. Roeder, B. Rogé, M. Rutter, S. Schlitt, N. Shah, V. Sheffield, L. Soorya, I. Sousa, Vera Stoppioni, N. Sykes, R. Tancredi, A. Thompson, Susanne A. Thomson, A. Tryfon, J. Tsiantis, H. van Engeland, J. Vincent, F. Volkmar, J. Vorstman, S. Wallace, Kirsty Wing, Kerstin Wittemeyer, Shawn Wood, Danielle M Zurawiecki, L. Zwaigenbaum, A. Bailey, A. Battaglia, R. Cantor, H. Coon, M. Cuccaro, G. Dawson, S. Ennis, C. Freitag, D. Geschwind, J. Haines, S. Klauck, W. McMahon, E. Maestrini, Judith S Miller, A. Monaco, S. Nelson, J. Nurnberger, G. Oliveira, J. Parr, M. Pericak-Vance, J. Piven, G. Schellenberg, S. Scherer, A. Vicente, T. Wassink, E. Wijsman, C. Betancur, J. Buxbaum, E. Cook, L. Gallagher, M. Gill, Joachim Hallmayer, A. Paterson, J. Sutcliffe, P. Szatmari, V. Vieland, H. Hakonarson, B. Devlin
8 2012
8
🐜
🐜 Variable expression of the autism broader phenotype: findings from extended pedigrees.
8 auth. A. Pickles, Elizabeth M. Starr, S. Kazak, P. Bolton, K. Papanikolaou, A. Bailey, ... R. Goodman, Michael Rutter
8 2000
8
🐜
🐜 A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
126 auth. J. Casey, T. Magalhães, J. Conroy, R. Regan, N. Shah, R. Anney, D. Shields, B. Abrahams, J. Almeida, E. Bacchelli, A. Bailey, G. Baird, A. Battaglia, T. Berney, N. Bolshakova, ... P. Bolton, T. Bourgeron, Sean Brennan, Philip W. Cali, C. Correia, Christina M. Corsello, M. Coutanche, G. Dawson, M. D. de Jonge, R. Delorme, E. Duketis, F. Duque, A. Estes, Penny Farrar, B. Fernandez, S. Folstein, S. Foley, E. Fombonne, C. Freitag, J. Gilbert, C. Gillberg, J. Glessner, Jonathan Green, Stephen J. Guter, H. Hakonarson, R. Holt, G. Hughes, Vanessa Hus, R. Igliozzi, Cecilia Kim, S. Klauck, A. Kolevzon, J. Lamb, M. Leboyer, A. Le Couteur, B. Leventhal, C. Lord, Sabata C. Lund, E. Maestrini, Carine Mantoulan, C. Marshall, H. McConachie, C. McDougle, J. McGrath, W. McMahon, Alison K. Merikangas, Judith S Miller, Fiorella Minopoli, G. Mirza, J. Munson, S. Nelson, G. Nygren, G. Oliveira, A. Pagnamenta, K. Papanikolaou, J. Parr, B. Parrini, A. Pickles, D. Pinto, J. Piven, D. Posey, A. Poustka, F. Poustka, J. Ragoussis, B. Rogé, M. Rutter, A. Sequeira, L. Soorya, I. Sousa, N. Sykes, Vera Stoppioni, R. Tancredi, M. Tauber, A. Thompson, Susanne A. Thomson, J. Tsiantis, H. van Engeland, J. Vincent, F. Volkmar, J. Vorstman, S. Wallace, Kai Wang, T. Wassink, K. White, Kirsty Wing, Kerstin Wittemeyer, B. Yaspan, L. Zwaigenbaum, C. Betancur, J. Buxbaum, R. Cantor, E. Cook, H. Coon, M. Cuccaro, D. Geschwind, J. Haines, Joachim Hallmayer, A. Monaco, J. Nurnberger, M. Pericak-Vance, G. Schellenberg, S. Scherer, J. Sutcliffe, P. Szatmari, V. Vieland, E. Wijsman, A. Green, M. Gill, L. Gallagher, A. Vicente, S. Ennis
7 2011
7
🐜
🐜 Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.
67 auth. S. Palferman, Nicola Matthews, M. Turner, Janette Moore, A. Hervás, Anne Aubin, S. Wallace, J. Michelotti, Catherine Wainhouse, A. Paul, E. Thompson, Marianne Murin, Ramyani P Gupta, C. Garner, A. Pickles, ... M. Rutter, A. Bailey, J. Lamb, A. Marlow, Pat Scudder, G. Barnby, A. Monaco, G. Baird, A. Cox, Z. Docherty, P. Warburton, Elizabeth P. Green, S. Abbs, H. McConachie, T. Berney, T. Kelly, P. Vries, P. Bolton, Jonathan Green, A. Gilchrist, J. Whittacker, Bryan D. Bolton, R. Packer, H. Engeland, M. Jonge, S. Klauck, K. S. Beyer, Sabine Epp, A. Poustka, A. Benner, F. Poustka, D. Rühl, E. Fombonne, Jeanne Fremolle-Kruck, C. Pienkowski, M. Tauber, Lennart Pedersen, G. Eriksen, J. Tsiantis, K. Papanikolaou, C. Lord, Christina M. Corsello, Stephen J. Guter, B. Leventhal, S. Smalley, J. Bailey, Amy Liu, Martha Dedricks, Lisa Chrzanowski, J. Levitt, D. Pauls, F. Volkmar
7 2001
7
🐜
🐜 High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility
72 auth. R. Holt, Kirsty Wing, Michael Rutter, J. Parr, S. Wallace, K. White, M. Coutanche, Suzanne Foley, Katy Renshaw, Kerstin Wittemeyer, Magdalena Laskawiec, P. Bolton, G. Baird, V. Slonims, Z. Docherty, ... S. Abbs, C. Ogilvie, P. Warburton, A. Pickles, Jonathan Green, C. Aldred, J. Wilkinson, A. Couteur, Tomi D. Berney, H. McConachie, E. Weisblatt, Lennart Pedersen, D. Haracopos, T. Isager, Birgitte Viskum, E. Sørensen, K. Brøndum‐Nielsen, B. Rogé, Jeanne Fremolle-Kruck, Carine Mantoulan, Inci Unsaldi-Cordier, F. Poustka, Gabriele Schmoetzer, E. Duketis, Sven Boelte, Sabine Feineis Matthews, S. Schlitt, A. Poustka, S. Klauck, B. Felder, G. Pakalapati, J. Tsiantis, K. Papanikolaou, E. Giouroukou, Elena Paliokosta, Simona Carone, F. Blasi, Fiorella Minopoli, A. Battaglia, T. Filippi, R. Tancredi, B. Parrini, R. Igliozzi, H. Engeland, M. Jonge, C. Kemner, M. Langemeijer, Channa T. Hijmans, F. Koop, W. Staal, C. Lord, E. Cook, Stephen J. Guter, Jeff Salt, Bennett L. Leventhal, F. Volkmar, E. Fombonne
7 2009
7
🐜
🐬 Association Between Family Divorce and Children's BMI and Meal Patterns: The GENDAI Study
M. Yannakoulia, K. Papanikolaou, Ioanna Hatzopoulou, E. Efstathiou, C. Papoutsakis, G. Dedoussis
6 2008
6
🐬
🦁 Using the Autism Diagnostic Interview-Revised and the Autism Diagnostic Observation Schedule-Generic for the Diagnosis of Autism Spectrum Disorders in a Greek Sample with a Wide Range of Intellectual Abilities
8 auth. K. Papanikolaou, Elena Paliokosta, G. Houliaras, Sofia Vgenopoulou, E. Giouroukou, A. Pehlivanidis, ... V. Tomaras, Ioannis Tsiantis
6 2009
6
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