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Refinado por: Nome da Publicação: American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics remover assunto: Biological And Medical Sciences remover
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1
Genome-wide association study in German patients with attention deficit/hyperactivity disorder
Genome-wide association study in German patients with attention deficit/hyperactivity disorder
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Genome-wide association study in German patients with attention deficit/hyperactivity disorder

Hinney, Anke ; Scherag, André ; Jarick, Ivonne ; Albayrak, Özgür ; Pütter, Carolin ; Pechlivanis, Sonali ; Dauvermann, Maria R. ; Beck, Sebastian ; Weber, Heike ; Scherag, Susann ; Nguyen, Trang T. ; Volckmar, Anna-Lena ; Knoll, Nadja ; Faraone, Stephen V. ; Neale, Benjamin M. ; Franke, Barbara ; Cichon, Sven ; Hoffmann, Per ; Nöthen, Markus M. ; Schreiber, Stefan ; Jöckel, Karl-Heinz ; Wichmann, H.-Erich ; Freitag, Christine ; Lempp, Thomas ; Meyer, Jobst ; Gilsbach, Susanne ; Herpertz-Dahlmann, Beate ; Sinzig, Judith ; Lehmkuhl, Gerd ; Renner, Tobias J. ; Warnke, Andreas ; Romanos, Marcel ; Lesch, Klaus-Peter ; Reif, Andreas ; Schimmelmann, Benno G. ; Hebebrand, Johannes

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-12, Vol.156B (8), p.888-897 [Periódico revisado por pares]

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2
No evidence that extended tracts of homozygosity are associated with Alzheimer's disease
No evidence that extended tracts of homozygosity are associated with Alzheimer's disease
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No evidence that extended tracts of homozygosity are associated with Alzheimer's disease

Sims, Rebecca ; Dwyer, Sarah ; Harold, Denise ; Gerrish, Amy ; Hollingworth, Paul ; Chapman, Jade ; Jones, Nicola ; Abraham, Richard ; Ivanov, Dobril ; Pahwa, Jaspreet Singh ; Moskvina, Valentina ; Dowzell, Kimberley ; Thomas, Charlene ; Stretton, Alexandra ; Lovestone, Simon ; Powell, John ; Proitsi, Petroula ; Lupton, Michelle K. ; Brayne, Carol ; Rubinsztein, David C. ; Gill, Michael ; Lawlor, Brian ; Lynch, Aoibhinn ; Morgan, Kevin ; Brown, Kristelle S. ; Passmore, Peter A. ; Craig, David ; McGuiness, Bernadette ; Todd, Stephen ; Johnston, Janet A. ; Holmes, Clive ; Mann, David ; Smith, A. David ; Love, Seth ; Kehoe, Patrick G. ; Hardy, John ; Mead, Simon ; Fox, Nick ; Rossor, Martin ; Collinge, John ; Livingston, Gill ; Bass, Nicholas J. ; Gurling, Hugh ; McQuillin, Andrew ; Jones, Lesley ; Holmans, Peter A. ; O'Donovan, Michael ; Owen, Michael J. ; Williams, Julie

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-12, Vol.156B (7), p.764-771 [Periódico revisado por pares]

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3
The role of ECE1 variants in cognitive ability in old age and Alzheimer's disease risk
The role of ECE1 variants in cognitive ability in old age and Alzheimer's disease risk
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The role of ECE1 variants in cognitive ability in old age and Alzheimer's disease risk

Hamilton, Gillian ; Harris, Sarah E. ; Davies, Gail ; Liewald, David C. ; Tenesa, Albert ; Payton, Antony ; Horan, Michael A. ; Ollier, William E.R. ; Pendleton, Neil ; Starr, John M. ; Porteous, David ; Deary, Ian J.

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2012-09, Vol.159B (6), p.696-709 [Periódico revisado por pares]

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4
A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12
A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12
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A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12

Butler, Amy W. ; Breen, Gerome ; Tozzi, Federica ; Craddock, Nick ; Gill, Mike ; Korszun, Ania ; Maier, Wolfgang ; Middleton, Lefkos T. ; Mors, Ole ; Owen, Michael J. ; Perry, Julia ; Preisig, Martin ; Rice, John P. ; Rietschel, Marcella ; Jones, Lisa ; Farmer, Anne E. ; Lewis, Cathryn M. ; McGuffin, Peter

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-12, Vol.153B (8), p.1465-1473 [Periódico revisado por pares]

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5
Dissecting the Genetic Heterogeneity of Depression Through Age at Onset
Dissecting the Genetic Heterogeneity of Depression Through Age at Onset
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Dissecting the Genetic Heterogeneity of Depression Through Age at Onset

Power, Robert A. ; Keers, Robert ; Ng, Mandy Y. ; Butler, Amy W. ; Uher, Rudolf ; Cohen-Woods, Sarah ; Ising, Marcus ; Craddock, Nick ; Owen, Michael J. ; Korszun, Ania ; Jones, Lisa ; Jones, Ian ; Gill, Michael ; Rice, John P. ; Hauser, Joanna ; Henigsberg, Neven ; Maier, Wolfgang ; Zobel, Astrid ; Mors, Ole ; Placentino, Anna S. ; Rietschel, Marcella ; Souery, Daniel ; Kozel, Dejan ; Preisig, Martin ; Lucae, Susanne ; Binder, Elisabeth B. ; Aitchison, Katherine J. ; Tozzi, Federica ; Muglia, Pierandrea ; Breen, Gerome ; Craig, Ian W. ; Farmer, Anne E. ; Müller-Myhsok, Bertram ; McGuffin, Peter ; Lewis, Cathryn M.

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2012-10, Vol.159B (7), p.859-868 [Periódico revisado por pares]

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6
Association of DRD4 in children with ADHD and comorbid conduct problems
Association of DRD4 in children with ADHD and comorbid conduct problems
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Association of DRD4 in children with ADHD and comorbid conduct problems

Holmes, Jane ; Payton, Antony ; Barrett, Jennifer ; Harrington, Richard ; McGuffin, Peter ; Owen, Michael ; Ollier, William ; Worthington, Jane ; Gill, Michael ; Kirley, Aiveen ; Hawi, Ziarih ; Fitzgerald, Michael ; Asherson, Philip ; Curran, Sarah ; Mill, John ; Gould, Alison ; Taylor, Eric ; Kent, Lyndsey ; Craddock, Nick ; Thapar, Anita

American journal of medical genetics, 2002-03, Vol.114 (2), p.150-153 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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7
Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1
Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1
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Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1

Dawson, Elisabeth ; Parfitt, Elizabeth ; Roberts, Queta ; Daniels, Jo ; Lim, Lionel ; Sham, Pak ; Nöthen, Markus ; Propping, Peter ; Lanczik, Mario ; Maier, Wolfgang ; Reuner, Ulrike ; Weissenbach, Jean ; Gill, Michael ; Powell, John ; McGuffin, Peter ; Owen, Mike ; Craddock, Nick

American journal of medical genetics, 1995-04, Vol.60 (2), p.94-102 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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8
A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12
A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12
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A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12

Gill, Michael ; Vallada, Homero ; Collier, David ; Sham, Pak ; Holmans, Peter ; Murray, Robin ; McGuffin, Peter ; Nanko, Shin ; Owen, Mike ; Antonarakis, Stylianos ; Housman, David ; Kazazian, Haig ; Nestadt, Gerald ; Pulver, Ann E. ; Straub, Richard E. ; MacLean, Charles J. ; Walsh, Dermot ; Kendler, Kenneth S. ; DeLisi, Lynn ; Polymeropoulos, Mihael ; Coon, Hilary ; Byerley, William ; Lofthouse, Ray ; Gershon, Elliot ; Golden, Lynn ; Crow, Timothy ; Byerley, William ; Freedman, Robert ; Laurent, Claudine ; Bodeau-Pean, Sylvie ; d'Amato, Thierry ; Jay, Maurice ; Campion, Dominique ; Mallet, Jacques ; Wildenauer, Dieter B. ; Lerer, Bernard ; Albus, Margot ; Ackenheil, Manfred ; Ebstein, Richard P. ; Hallmayer, Joachim ; Maier, Wolfgang ; Gurling, Hugh ; Curtis, David ; Kalsi, Gusharon ; Brynjolfsson, Jon ; Sigmundson, Thordur ; Petursson, Hannes ; Blackwood, Douglas ; Muir, Walter ; St. Clair, David ; He, Lin ; Maguire, Susan ; Moises, Hans W. ; Hwu, Hai-Gwo ; Yang, Liu ; Wiese, Claudia ; Tao, Li ; Liu, Xiehe ; Kristbjarnason, Helgi ; Levinson, Douglas F. ; Mowry, Bryan J. ; Donis-Keller, Helen ; Hayward, Nicholas K. ; Crowe, Raymond R. ; Silverman, Jeremy M. ; Nancarrow, Derek J. ; Read, Christina M.

American journal of medical genetics, 1996-02, Vol.67 (1), p.40-45 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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9
Linkage studies on chromosome 22 in familial schizophrenia
Linkage studies on chromosome 22 in familial schizophrenia
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Linkage studies on chromosome 22 in familial schizophrenia

Vallada, Homero P. ; Gill, Michael ; Sham, Pak ; Lim, Lionel C. C. ; Nanko, Shin ; Asherson, Philip ; Murray, Robin M. ; McGuffin, Peter ; Owen, Michael ; Collier, David

American journal of medical genetics, 1995-04, Vol.60 (2), p.139-146 [Periódico revisado por pares]

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10
DSM-IV Combined Type ADHD Shows Familial Association With Sibling Trait Scores : A Sampling Strategy For QTL Linkage: Special Issue on the Genetics of ADHD Dedicated to the Memory of Richard Todd
DSM-IV Combined Type ADHD Shows Familial Association With Sibling Trait Scores : A Sampling Strategy For QTL Linkage: Special Issue on the Genetics of ADHD Dedicated to the Memory of Richard Todd
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DSM-IV Combined Type ADHD Shows Familial Association With Sibling Trait Scores : A Sampling Strategy For QTL Linkage: Special Issue on the Genetics of ADHD Dedicated to the Memory of Richard Todd

WAI CHEN ; KAIXIN ZHOU ; ALTINK, Marieke ; BOER, Frits ; BOHOLST, Mary Jane ; BUSCHGENS, Cathelijne ; BUTLER, Louise ; CHRISTIANSEN, Hanna ; FLIERS, Ellen ; HOWE-FORBES, Raoul ; GABRIËLS, Isabel ; HEISE, Alexander ; SHAM, Pak ; KORN-LUBETZKI, Isabelle ; MARCO, Rafaela ; MEDAD, Sheera ; MINDERAA, Ruud ; MULLER, Ueli C ; MULLIGAN, Aisling ; PSYCHOGIOU, Lamprini ; ROMMELSE, Nanda ; SETHNA, Vaheshta ; UEBEL, Henrik ; FRANKE, Barbara ; MEGUFFIN, Peter ; PLOMIN, Robert ; BANASCHEWSKI, Tobias ; BUITELAAR, Jan ; EBSTEIN, Richard ; EISENBERG, Jacques ; GILL, Michael ; MANOR, Iris ; MIRANDA, Ana ; MULAS, Fernando ; KUNTSI, Jonna ; OADES, Robert D ; ROEYERS, Herbert ; ROTHENBERGER, Aribert ; SERGEANT, Joseph ; SONUGA-BARKE, Edmund ; STEINHAUSEN, Hans-Christoph ; TAYLOR, Eric ; THOMPSON, Margaret ; FARAONE, Stephen V ; ASHERSONL, Philip ; CAMPBELL, Desmond ; FLEISCHMAN, Karin ; KNIGHT, Jo ; ANDREOU, Penny ; ARNOLD, Renée

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008, Vol.147 (8), p.1450-1460 [Periódico revisado por pares]

Hoboken, NJ: Wiley-Liss

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