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1

Chipping away at the old block حسب Nigel Williams

منشور في 2003

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Artigo

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2

Is the Dysbindin Gene (DTNBP1) a Susceptibility Gene for Schizophrenia? حسب Nigel Williams

منشور في 2005

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Revisão

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3

Spontaneous pneumoperitoneum and other nonsurgical causes of intraperitoneal free gas حسب Nigel Williams, D F L Watkin

منشور في 1997

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Revisão

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4

The molecular genetics of schizophrenia: new findings promise new insights حسب Michael J. Owen, Nigel Williams, Michael O’Donovan

منشور في 2003

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Revisão

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5

Recent advances in the genetics of schizophrenia حسب Michael O’Donovan, Nigel Williams, M J Owen

منشور في 2003

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Revisão

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6

The relative contribution of common and rare genetic variants to ADHD حسب Joanna Martin, Michael O’Donovan, Anita Thapar, K. Langley, Nigel Williams

منشور في 2015

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Artigo

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7

Substance, structure and stigma: Parents in the UK accounting for opioid substitution therapy during the antenatal and postnatal periods حسب Amy Chandler, Anne Whittaker, Sarah Cunningham‐Burley, Nigel Williams, Kelly McGorm, Gillian Mathews

منشور في 2013

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Artigo

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8

Concentration-effect relationships with carbamazepine and its epoxide on psychomotor and cognitive function in epileptic patients. حسب Ruth Gillham, Nigel Williams, Klaus D. Wiedmann, Elaine Butler, John G. Larkin, M J Brodie

منشور في 1988

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Artigo

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9

A Simple Method for Analyzing Microsatellite Allele Image Patterns Generated from DNA Pools and Its Application to Allelic Association Studies حسب Johanna Daniels, Peter Holmans, Nigel Williams, Dragana Turic, Peter McGuffin, Robert Plomin, Michael J. Owen

منشور في 1998

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Artigo

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10

Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use حسب Stanley Zammit, Gillian Spurlock, Hywel Williams, Nadine Norton, Nigel Williams, Michael O’Donovan, Michael J. Owen

منشور في 2007

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Artigo

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11

Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney disease حسب Keshwar Baboolal, David Ravine, Joe Parkin Daniels, Nigel Williams, Peter Holmans, Gerald A. Coles, J. D. Williams

منشور في 1997

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Artigo

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12

A Haplotype Implicated in Schizophrenia Susceptibility Is Associated with Reduced COMT Expression in Human Brain حسب Nicholas J. Bray, Paul R. Buckland, Nigel Williams, Hywel Williams, Nadine Norton, Michael J. Owen, Michael O’Donovan

منشور في 2003

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Artigo

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13

Genetic risk and age in Parkinson's disease: Continuum not stratum حسب Mike A. Nalls, Valentina Escott‐Price, Nigel Williams, Steven Lubbe, Margaux F. Keller, Huw R. Morris, Andrew Singleton

منشور في 2015

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Artigo

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14

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression حسب Nicholas J. Bray, Anna Preece, Nigel Williams, Valentina Moskvina, Paul R. Buckland, Michael J. Owen, Michael O’Donovan

منشور في 2005

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Artigo

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15

Convergent Evidence for 2′,3′-Cyclic Nucleotide 3′-Phosphodiesterase as a Possible Susceptibility Gene for Schizophrenia حسب T Peirce, Nicholas J. Bray, Nigel Williams, Nadine Norton, Valentina Moskvina, Anna Preece, Vahram Haroutunian, Joseph D. Buxbaum, Michael J. Owen, Michael O’Donovan

منشور في 2006

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Artigo

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16

Epigenetic insights into neuropsychiatric and cognitive symptoms in Parkinson’s disease: A DNA co-methylation network analysis حسب Joshua Harvey, Adam R. Smith, Luke Weymouth, Rebecca G. Smith, Isabel Castanho, Leon Hubbard, Byron Creese, Catherine Bresner, Nigel Williams, Ehsan Pishva, Katie Lunnon

منشور في 2025

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Artigo

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17

Polygenic risk of <scp>P</scp>arkinson disease is correlated with disease age at onset حسب Valentina Escott‐Price, Mike A. Nalls, Huw R. Morris, Steven Lubbe, Alexis Brice, Thomas Gasser, Peter Heutink, Nicholas Wood, John Hardy, Andrew Singleton, Nigel Williams

منشور في 2015

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Artigo

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18

Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p حسب Justin Pearson, Nigel Williams, Elisa Majounie, Adrian J. Waite, J. Randall Stott, Victoria Newsway, Alex Murray, Dena Hernandez, Rita Guerreiro, Andrew Singleton, James Neal, Huw R. Morris

منشور في 2010

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Artigo

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19

Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD حسب Evie Stergiakouli, Marian L. Hamshere, Peter Holmans, K. Langley, Irina Zaharieva, Ziarih Hawi, Lindsey Kent, Michael Gill, Nigel Williams, Michael J. Owen, Michael O’Donovan, Anita Thapar

منشور في 2011

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Artigo

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20

C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism حسب Seán O’Dowd, Denis Curtin, Adrian J. Waite, Kinley Roberts, Niall Pender, Valerie Reid, Martin O’Connell, Nigel Williams, Huw R. Morris, Bryan J. Traynor, Timothy Lynch

منشور في 2012

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Carta

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Chipping away at the old block حسب Nigel Williams

Is the Dysbindin Gene (DTNBP1) a Susceptibility Gene for Schizophrenia? حسب Nigel Williams

Spontaneous pneumoperitoneum and other nonsurgical causes of intraperitoneal free gas حسب Nigel Williams, D F L Watkin

The molecular genetics of schizophrenia: new findings promise new insights حسب Michael J. Owen, Nigel Williams, Michael O’Donovan

Recent advances in the genetics of schizophrenia حسب Michael O’Donovan, Nigel Williams, M J Owen

The relative contribution of common and rare genetic variants to ADHD حسب Joanna Martin, Michael O’Donovan, Anita Thapar, K. Langley, Nigel Williams

Substance, structure and stigma: Parents in the UK accounting for opioid substitution therapy during the antenatal and postnatal periods حسب Amy Chandler, Anne Whittaker, Sarah Cunningham‐Burley, Nigel Williams, Kelly McGorm, Gillian Mathews

Concentration-effect relationships with carbamazepine and its epoxide on psychomotor and cognitive function in epileptic patients. حسب Ruth Gillham, Nigel Williams, Klaus D. Wiedmann, Elaine Butler, John G. Larkin, M J Brodie

A Simple Method for Analyzing Microsatellite Allele Image Patterns Generated from DNA Pools and Its Application to Allelic Association Studies حسب Johanna Daniels, Peter Holmans, Nigel Williams, Dragana Turic, Peter McGuffin, Robert Plomin, Michael J. Owen

<b>Genotype effects of <i>CHRNA7, CNR1</i> and <i>COMT</i> in schizophrenia: interactions with tobacco and cannabis use</b> حسب Stanley Zammit, Gillian Spurlock, Hywel Williams, Nadine Norton, Nigel Williams, Michael O’Donovan, Michael J. Owen

Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney disease حسب Keshwar Baboolal, David Ravine, Joe Parkin Daniels, Nigel Williams, Peter Holmans, Gerald A. Coles, J. D. Williams

A Haplotype Implicated in Schizophrenia Susceptibility Is Associated with Reduced COMT Expression in Human Brain حسب Nicholas J. Bray, Paul R. Buckland, Nigel Williams, Hywel Williams, Nadine Norton, Michael J. Owen, Michael O’Donovan

Genetic risk and age in Parkinson's disease: Continuum not stratum حسب Mike A. Nalls, Valentina Escott‐Price, Nigel Williams, Steven Lubbe, Margaux F. Keller, Huw R. Morris, Andrew Singleton

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression حسب Nicholas J. Bray, Anna Preece, Nigel Williams, Valentina Moskvina, Paul R. Buckland, Michael J. Owen, Michael O’Donovan

Polygenic risk of <scp>P</scp>arkinson disease is correlated with disease age at onset حسب Valentina Escott‐Price, Mike A. Nalls, Huw R. Morris, Steven Lubbe, Alexis Brice, Thomas Gasser, Peter Heutink, Nicholas Wood, John Hardy, Andrew Singleton, Nigel Williams

Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD حسب Evie Stergiakouli, Marian L. Hamshere, Peter Holmans, K. Langley, Irina Zaharieva, Ziarih Hawi, Lindsey Kent, Michael Gill, Nigel Williams, Michael J. Owen, Michael O’Donovan, Anita Thapar

<i>C9ORF72</i> expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism حسب Seán O’Dowd, Denis Curtin, Adrian J. Waite, Kinley Roberts, Niall Pender, Valerie Reid, Martin O’Connell, Nigel Williams, Huw R. Morris, Bryan J. Traynor, Timothy Lynch

نتائج البحث - Nigel Williams

Chipping away at the old block حسب Nigel Williams

Is the Dysbindin Gene (DTNBP1) a Susceptibility Gene for Schizophrenia? حسب Nigel Williams

Spontaneous pneumoperitoneum and other nonsurgical causes of intraperitoneal free gas حسب Nigel Williams, D F L Watkin

The molecular genetics of schizophrenia: new findings promise new insights حسب Michael J. Owen, Nigel Williams, Michael O’Donovan

Recent advances in the genetics of schizophrenia حسب Michael O’Donovan, Nigel Williams, M J Owen

The relative contribution of common and rare genetic variants to ADHD حسب Joanna Martin, Michael O’Donovan, Anita Thapar, K. Langley, Nigel Williams

Substance, structure and stigma: Parents in the UK accounting for opioid substitution therapy during the antenatal and postnatal periods حسب Amy Chandler, Anne Whittaker, Sarah Cunningham‐Burley, Nigel Williams, Kelly McGorm, Gillian Mathews

Concentration-effect relationships with carbamazepine and its epoxide on psychomotor and cognitive function in epileptic patients. حسب Ruth Gillham, Nigel Williams, Klaus D. Wiedmann, Elaine Butler, John G. Larkin, M J Brodie

A Simple Method for Analyzing Microsatellite Allele Image Patterns Generated from DNA Pools and Its Application to Allelic Association Studies حسب Johanna Daniels, Peter Holmans, Nigel Williams, Dragana Turic, Peter McGuffin, Robert Plomin, Michael J. Owen

<b>Genotype effects of <i>CHRNA7, CNR1</i> and <i>COMT</i> in schizophrenia: interactions with tobacco and cannabis use</b> حسب Stanley Zammit, Gillian Spurlock, Hywel Williams, Nadine Norton, Nigel Williams, Michael O’Donovan, Michael J. Owen

Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney disease حسب Keshwar Baboolal, David Ravine, Joe Parkin Daniels, Nigel Williams, Peter Holmans, Gerald A. Coles, J. D. Williams

A Haplotype Implicated in Schizophrenia Susceptibility Is Associated with Reduced COMT Expression in Human Brain حسب Nicholas J. Bray, Paul R. Buckland, Nigel Williams, Hywel Williams, Nadine Norton, Michael J. Owen, Michael O’Donovan

Genetic risk and age in Parkinson's disease: Continuum not stratum حسب Mike A. Nalls, Valentina Escott‐Price, Nigel Williams, Steven Lubbe, Margaux F. Keller, Huw R. Morris, Andrew Singleton

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression حسب Nicholas J. Bray, Anna Preece, Nigel Williams, Valentina Moskvina, Paul R. Buckland, Michael J. Owen, Michael O’Donovan

Polygenic risk of <scp>P</scp>arkinson disease is correlated with disease age at onset حسب Valentina Escott‐Price, Mike A. Nalls, Huw R. Morris, Steven Lubbe, Alexis Brice, Thomas Gasser, Peter Heutink, Nicholas Wood, John Hardy, Andrew Singleton, Nigel Williams

Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD حسب Evie Stergiakouli, Marian L. Hamshere, Peter Holmans, K. Langley, Irina Zaharieva, Ziarih Hawi, Lindsey Kent, Michael Gill, Nigel Williams, Michael J. Owen, Michael O’Donovan, Anita Thapar

<i>C9ORF72</i> expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism حسب Seán O’Dowd, Denis Curtin, Adrian J. Waite, Kinley Roberts, Niall Pender, Valerie Reid, Martin O’Connell, Nigel Williams, Huw R. Morris, Bryan J. Traynor, Timothy Lynch

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