Peter Robert Schofield
#134,833
Most Influential Person Now
Peter Robert Schofield's AcademicInfluence.com Rankings
Peter Robert Schofieldphilosophy Degrees
Philosophy
#6746
World Rank
#9841
Historical Rank
Logic
#3867
World Rank
#5090
Historical Rank
Peter Robert Schofieldbiology Degrees
Biology
#9145
World Rank
#12315
Historical Rank
Neuroscience
#1314
World Rank
#1359
Historical Rank
Download Badge
Philosophy Biology
Peter Robert Schofield's Degrees
- PhD Neuroscience University of California, San Francisco
- Doctorate Medicine Stanford University
Why Is Peter Robert Schofield Influential?
(Suggest an Edit or Addition)Peter Robert Schofield's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 (1998) (3363)
- Clinical and biomarker changes in dominantly inherited Alzheimer's disease. (2012) (2815)
- Analysis of shared heritability in common disorders of the brain (2016) (1385)
- Importance of a novel GABAA receptor subunit for benzodiazepine pharmacology (1989) (1327)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
- Common genetic variants influence human subcortical brain structures (2015) (731)
- Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data (2014) (646)
- Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. (2003) (592)
- Two novel GABAA receptor subunits exist in distinct neuronal subpopulations (1989) (533)
- Interactions between BDNF Val66Met polymorphism and early life stress predict brain and arousal pathways to syndromal depression and anxiety (2009) (518)
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
- Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer’s disease (2019) (487)
- Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer’s disease (2019) (487)
- Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group (2017) (482)
- Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (2018) (417)
- The genetic architecture of the human cerebral cortex (2018) (355)
- White matter hyperintensities are a core feature of Alzheimer's disease: Evidence from the dominantly inherited Alzheimer network (2016) (341)
- Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report (2013) (340)
- Symptom onset in autosomal dominant Alzheimer disease (2014) (338)
- Longitudinal Change in CSF Biomarkers in Autosomal-Dominant Alzheimer’s Disease (2014) (335)
- Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949) (2015) (328)
- The glycine receptor. (1997) (325)
- Regional variability of imaging biomarkers in autosomal dominant Alzheimer’s disease (2013) (318)
- Spatial patterns of neuroimaging biomarker change in individuals from families with autosomal dominant Alzheimer disease: a longitudinal study (2018) (316)
- Life events, first depression onset and the serotonin transporter gene (2006) (315)
- Genome-wide association study reveals two new risk loci for bipolar disorder (2014) (311)
- Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. (2011) (286)
- Frontotemporal dementia and its subtypes: a genome-wide association study (2014) (262)
- Genetics of dementia (2013) (259)
- Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study (2016) (258)
- A soluble phosphorylated tau signature links tau, amyloid and the evolution of stages of dominantly inherited Alzheimer’s disease (2020) (252)
- A soluble phosphorylated tau signature links tau, amyloid and the evolution of stages of dominantly inherited Alzheimer’s disease (2020) (252)
- Specific and common genes implicated across major mental disorders: a review of meta-analysis studies. (2015) (250)
- Transient expression shows ligand gating and allosteric potentiation of GABAA receptor subunits. (1988) (247)
- Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) (240)
- Novel genetic loci associated with hippocampal volume (2017) (238)
- Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene (2000) (223)
- Identification of intracellular and extracellular domains mediating signal transduction in the inhibitory glycine receptor chloride channel (1997) (222)
- Molecular evidence of N-methyl-D-aspartate receptor hypofunction in schizophrenia (2012) (220)
- Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative (2007) (218)
- Structural and functional characterization of the gamma 1 subunit of GABAA/benzodiazepine receptors. (1990) (207)
- Ligand-gated ion channels: mechanisms underlying ion selectivity. (2004) (205)
- GSK3B polymorphisms alter transcription and splicing in Parkinson's disease (2005) (204)
- Novel genetic loci underlying human intracranial volume identified through genome-wide association (2016) (192)
- Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration–motor neuron disease (2010) (192)
- Developing an international network for Alzheimer research: The Dominantly Inherited Alzheimer Network. (2012) (186)
- Partial volume correction in quantitative amyloid imaging (2015) (182)
- Heterozygous neuregulin 1 mice are more sensitive to the behavioural effects of Δ9-tetrahydrocannabinol (2007) (177)
- Two novel (M233T and ρ278T) presenilin‐1 mutations in early‐onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin‐1 mutations with a novel phenotype (1997) (171)
- A missense mutation in the gene encoding the α1 subunit of the inhibitory glycine receptor in the spasmodic mouse (1994) (169)
- Altered motor activity, exploration and anxiety in heterozygous neuregulin 1 mutant mice: implications for understanding schizophrenia (2007) (165)
- Longitudinal cognitive and biomarker changes in dominantly inherited Alzheimer disease (2018) (163)
- Tau haplotypes regulate transcription and are associated with Parkinson's disease (2004) (161)
- Molecular cloning and amino acid sequence of rat enkephalinase. (1987) (158)
- Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations. (2000) (157)
- A single amino acid determines differences in ethanol actions on strychnine-sensitive glycine receptors. (1996) (156)
- Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB). (2002) (153)
- Mutation of an arginine residue in the human glycine receptor transforms β-alanine and taurine from agonists into competitive antagonists (1995) (153)
- Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. (2016) (153)
- Hedgehog overexpression is associated with stromal interactions and predicts for poor outcome in breast cancer. (2011) (151)
- Functional chloride channels by mammalian cell expression of rat glycine receptor subunit (1989) (149)
- Genetic architecture of subcortical brain structures in 38,851 individuals (2019) (148)
- Impaired default network functional connectivity in autosomal dominant Alzheimer disease (2013) (146)
- Structure of the precursor to an enzyme mediating COOH-terminal amidation in peptide biosynthesis. (1987) (142)
- The contribution of apolipoprotein E alleles on cognitive performance and dynamic neural activity over six decades (2007) (141)
- Brain aging in major depressive disorder: results from the ENIGMA major depressive disorder working group (2019) (140)
- The Brain-Derived Neurotrophic Factor Val66Met Polymorphism Predicts Response to Exposure Therapy in Posttraumatic Stress Disorder (2013) (138)
- ‘Negativity bias’ in risk for depression and anxiety: Brain–body fear circuitry correlates, 5-HTT-LPR and early life stress (2009) (135)
- Distinct agonist- and antagonist-binding sites on the glycine receptor (1992) (133)
- Disturbances in selective information processing associated with the BDNF Val66Met polymorphism: Evidence from cognition, the P300 and fronto-hippocampal systems (2009) (130)
- Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia (2017) (129)
- Evidence for Genetic Exchange and Recombination of Rhizobium Symbiotic Plasmids in a Soil Population (1987) (128)
- Preclinical trials in autosomal dominant AD: implementation of the DIAN-TU trial. (2013) (127)
- Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia. (2003) (126)
- Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification (2013) (124)
- Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study (2017) (122)
- Serotonin transporter gene status predicts caudate nucleus but not amygdala or hippocampal volumes in older persons with major depression. (2007) (122)
- Mutations Affecting the Glycine Receptor Agonist Transduction Mechanism Convert the Competitive Antagonist, Picrotoxin, into an Allosteric Potentiator (*) (1995) (119)
- Startle disease mutations reduce the agonist sensitivity of the human inhibitory glycine receptor. (1994) (118)
- M2 pore mutations convert the glycine receptor channel from being anion- to cation-selective. (2000) (118)
- Adjunctive raloxifene treatment improves attention and memory in men and women with schizophrenia (2015) (117)
- Antagonism of ligand-gated ion channel receptors: two domains of the glycine receptor alpha subunit form the strychnine-binding site. (1992) (113)
- Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic disease (1989) (113)
- C9ORF72 repeat expansion in clinical and neuropathologic frontotemporal dementia cohorts (2012) (110)
- The GABAA receptor: molecular biology reveals a complex picture. (1989) (107)
- COMT Val108/158Met polymorphism effects on emotional brain function and negativity bias (2010) (106)
- Implications of genetic risk information in families with a high density of bipolar disorder: an exploratory study. (2005) (106)
- Specific roles for the asparagine-linked carbohydrate residues of recombinant human follicle stimulating hormone in receptor binding and signal transduction. (1994) (106)
- Functional connectivity in autosomal dominant and late-onset Alzheimer disease. (2014) (106)
- Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals (2019) (105)
- Preliminary Evidence of the Short Allele of the Serotonin Transporter Gene Predicting Poor Response to Cognitive Behavior Therapy in Posttraumatic Stress Disorder (2010) (103)
- DNA sequence of Rhizobium trifolii nodulation genes reveals a reiterated and potentially regulatory sequence preceding nodABC and nodFE. (1986) (103)
- Mutations in progranulin explain atypical phenotypes with variants in MAPT. (2006) (102)
- Common variant at 16p11.2 conferring risk of psychosis (2014) (100)
- The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
- Cation-selective Mutations in the M2 Domain of the Inhibitory Glycine Receptor Channel Reveal Determinants of Ion-Charge Selectivity (2002) (98)
- BDNF Val66Met Polymorphism Is Associated with Body Mass Index in Healthy Adults (2006) (97)
- Pedigree with frontotemporal lobar degeneration – motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9 (2008) (97)
- Novel Leu723Pro amyloid precursor protein mutation increases amyloid β42(43) peptide levels and induces apoptosis (2000) (94)
- Widespread expression of GABAA receptor subunits in peripheral tissues (1999) (94)
- A threonine residue in the seventh transmembrane domain of the human A1 adenosine receptor mediates specific agonist binding. (1994) (94)
- White matter diffusion alterations precede symptom onset in autosomal dominant Alzheimer’s disease (2018) (93)
- The role of receptor subtype diversity in the CNS (1990) (91)
- A susceptibility locus for bipolar affective disorder on chromosome 4q35. (1998) (90)
- Virtual Histology of Cortical Thickness and Shared Neurobiology in 6 Psychiatric Disorders. (2020) (89)
- Early Life Stress Combined with Serotonin 3A Receptor and Brain-Derived Neurotrophic Factor Valine 66 to Methionine Genotypes Impacts Emotional Brain and Arousal Correlates of Risk for Depression (2010) (89)
- The human glycine receptor beta subunit: primary structure, functional characterisation and chromosomal localisation of the human and murine genes. (1996) (87)
- Variable phenotype of Alzheimer's disease with spastic paraparesis (2001) (87)
- A Polymorphism of the MAOA Gene is Associated with Emotional Brain Markers and Personality Traits on an Antisocial Index (2009) (87)
- Public interest in predictive genetic testing, including direct-to-consumer testing, for susceptibility to major depression: preliminary findings (2010) (85)
- Variation in the oxytocin receptor gene is associated with increased risk for anxiety, stress and depression in individuals with a history of exposure to early life stress. (2014) (83)
- Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia. (2018) (81)
- Sequence and expression of human GABAA receptor α1 and β1 subunits (1989) (81)
- Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss (2001) (81)
- Both of the beta-subunit carbohydrate residues of follicle-stimulating hormone determine the metabolic clearance rate and in vivo potency. (1995) (78)
- Identification of shared risk loci and pathways for bipolar disorder and schizophrenia (2017) (78)
- Zinc Potentiation of the Glycine Receptor Chloride Channel Is Mediated by Allosteric Pathways (1998) (76)
- The prevalence of SDHB, SDHC, and SDHD mutations in patients with head and neck paraganglioma and association of mutations with clinical features (2004) (75)
- Compound heterozygosity and nonsense mutations in the α1-subunit of the inhibitory glycine receptor in hyperekplexia (2001) (74)
- Association between BDNF Val66Met polymorphism and trait depression is mediated via resting EEG alpha band activity (2008) (73)
- Attitudes towards childbearing, causal attributions for bipolar disorder and psychological distress: a study of families with multiple cases of bipolar disorder (2007) (72)
- Schizophrenia-associated HapICE haplotype is associated with increased NRG1 type III expression and high nucleotide diversity (2012) (72)
- Left frontal hub connectivity delays cognitive impairment in autosomal-dominant and sporadic Alzheimer’s disease (2018) (71)
- Identification of Sialyltransferase 8B as a Generalized Susceptibility Gene for Psychotic and Mood Disorders on Chromosome 15q25-26 (2012) (70)
- Early behavioural changes in familial Alzheimer's disease in the Dominantly Inherited Alzheimer Network. (2015) (70)
- Role of Charged Residues in Coupling Ligand Binding and Channel Activation in the Extracellular Domain of the Glycine Receptor* (2003) (69)
- White matter hyperintensities and the mediating role of cerebral amyloid angiopathy in dominantly-inherited Alzheimer’s disease (2018) (68)
- The heritability of mental health and wellbeing defined using COMPAS-W, a new composite measure of wellbeing (2014) (68)
- The pattern of atrophy in familial Alzheimer disease (2013) (68)
- A Comprehensive Neuropsychiatric Study of Elderly Twins: The Older Australian Twins Study (2009) (67)
- The Surface Accessibility of the Glycine Receptor M2–M3 Loop Is Increased in the Channel Open State (2001) (67)
- Familial idiopathic basal ganglia calcification (Fahr's disease) without neurological, cognitive and psychiatric symptoms is not linked to the IBGC1 locus on chromosome 14q (2001) (67)
- Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors (2020) (66)
- Molecular mechanisms of inherited startle syndromes (1995) (65)
- A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19 (2002) (65)
- Memory decline in healthy older people (2001) (64)
- C9ORF72 Repeat Expansion in Australian and Spanish Frontotemporal Dementia Patients (2013) (64)
- Molecular biology of the GABAA receptor. (1988) (63)
- Preferential degradation of cognitive networks differentiates Alzheimer’s disease from ageing (2018) (63)
- Review and meta-analysis of genetic polymorphisms associated with exceptional human longevity (2018) (63)
- Glycogen synthase kinase‐3β and tau genes interact in Alzheimer's disease (2008) (62)
- Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele (2006) (62)
- Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder (2015) (61)
- Behavioral profile of a heterozygous mutant mouse model for EGF-like domain neuregulin 1. (2008) (60)
- BDNF Val66Met moderates memory impairment, hippocampal function and tau in preclinical autosomal dominant Alzheimer's disease. (2016) (59)
- Gating mechanisms in Cys-loop receptors (2009) (58)
- Two novel presenilin‐1 mutations (Ser169Leu and Pro436Gln) associated with very early onset Alzheimer's disease (1998) (57)
- Neurological manifestations of autosomal dominant familial Alzheimer’s disease: a comparison of the published literature with the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS) (2016) (57)
- Cerebral small vessel disease genomics and its implications across the lifespan (2020) (56)
- Distinct Physiological Mechanisms Underlie Altered Glycinergic Synaptic Transmission in the Murine Mutants spastic, spasmodic, and oscillator (2006) (56)
- Altered inhibitory synaptic transmission in superficial dorsal horn neurones in spastic and oscillator mice. (2003) (56)
- Alzheimer's disease with spastic paraparesis and 'cotton wool' plaques: two pedigrees with PS-1 exon 9 deletions. (2003) (55)
- Aging, exceptional longevity and comparisons of the Hannum and Horvath epigenetic clocks. (2017) (55)
- The integrate model of emotion, thinking and self regulation: an application to the "paradox of aging". (2008) (55)
- Isoelectric charge of recombinant human follicle-stimulating hormone isoforms determines receptor affinity and in vitro bioactivity. (1993) (55)
- The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders (2017) (54)
- Presenilin-1 Mutation L271V Results in Altered Exon 8 Splicing and Alzheimer's Disease with Non-cored Plaques and No Neuritic Dystrophy* (2003) (53)
- Pick bodies in a family with presenilin‐1 Alzheimer's disease (2005) (53)
- Thermodynamics of full agonist, partial agonist, and antagonist binding to wild-type and mutant adenosine A1 receptors. (1998) (52)
- Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility (2012) (52)
- CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis. (2020) (52)
- Tn5 mutagenesis of Rhizobium trifolii host-specific nodulation genes result in mutants with altered host-range ability (1985) (52)
- Kinetic Determinants of Agonist Action at the Recombinant Human Glycine Receptor (2003) (51)
- The startle disease mutation Q266H, in the second transmembrane domain of the human glycine receptor, impairs channel gating. (1999) (51)
- Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies (2004) (50)
- Associations between the COMT Val/Met polymorphism, early life stress, and personality among healthy adults (2006) (49)
- A novel subtype of muscarinic receptor identified by homology screening. (1987) (48)
- Microarray gene expression profiling of mouse brain mRNA in a model of lithium treatment (2008) (48)
- A Missense Mutation in Kynurenine Aminotransferase-1 in Spontaneously Hypertensive Rats* (2002) (48)
- Attitudes to genetic testing in families with multiple cases of bipolar disorder. (2008) (47)
- A Nonsense Mutation in the α1 Subunit of the Inhibitory Glycine Receptor Associated with Bovine Myoclonus (2001) (47)
- Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. (2020) (47)
- Memory decline in healthy older people: Implications for identifying mild cognitive impairment (2001) (47)
- The Association Between Familial Risk and Brain Abnormalities Is Disease Specific: An ENIGMA-Relatives Study of Schizophrenia and Bipolar Disorder (2019) (47)
- Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults (2020) (46)
- Quantitative Amyloid Imaging in Autosomal Dominant Alzheimer’s Disease: Results from the DIAN Study Group (2016) (46)
- Habitual exercise levels are associated with cerebral amyloid load in presymptomatic autosomal dominant Alzheimer's disease (2017) (46)
- The BDNFVal66Met SNP modulates the association between beta-amyloid and hippocampal disconnection in Alzheimer’s disease (2019) (46)
- Relationship between physical activity, cognition, and Alzheimer pathology in autosomal dominant Alzheimer's disease (2018) (46)
- The TWIN-E Project in Emotional Wellbeing: Study Protocol and Preliminary Heritability Results Across Four MRI and DTI Measures (2012) (45)
- The Genetics of White Matter Lesions (2011) (44)
- A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q (2001) (44)
- Characterization and chromosomal localization of the human A2a adenosine receptor gene: ADORA2A. (1996) (43)
- Single Channel Analysis of Conductance and Rectification in Cation-selective, Mutant Glycine Receptor Channels (2002) (43)
- Variable phenotype of Alzheimer’s disease with spastic paraparesis (2007) (42)
- The Long and the Short of It: Associations Between 5-HTT Genotypes and Coping With Stress (2007) (42)
- A meta-analysis of the risk of major affective disorder in relatives of individuals affected by major depressive disorder or bipolar disorder. (2014) (42)
- Nonparametric simulation-based statistical analyses for bipolar affective disorder locus on chromosome 21q22.3. (1999) (41)
- Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities (2020) (41)
- Decreased body mass index in the preclinical stage of autosomal dominant Alzheimer’s disease (2017) (40)
- Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region (1997) (40)
- Assessing oxidative pathway genes as risk factors for bipolar disorder. (2010) (40)
- Cloning, characterisation and chromosomal assignment of the human adenosine A3 receptor (ADORA3) gene 1 GenBank™ accession numbers: L77729 and L77730. 1 (1997) (40)
- Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2018) (40)
- Differences in regional brain atrophy in genetic forms of Alzheimer's disease (2006) (40)
- A genotype-endophenotype-phenotype path model of depressed mood: integrating cognitive and emotional markers. (2007) (39)
- Identification of a New Ligand Binding Domain in the α1 Subunit of the Inhibitory Glycine Receptor (1999) (39)
- Gene-microRNA interactions associated with antipsychotic mechanisms and the metabolic side effects of olanzapine (2013) (39)
- A Role for Transcription Factor GTF2IRD2 in Executive Function in Williams-Beuren Syndrome (2012) (39)
- Positional effects of presenilin-1 mutations on tau phosphorylation in cortical plaques (2004) (38)
- Exclusion of close linkage of bipolar disorder to the Gs-alpha subunit gene in nine Australian pedigrees. (1994) (38)
- Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At‐Risk Individuals (2015) (37)
- Association of polygenic score for major depression with response to lithium in patients with bipolar disorder (2020) (37)
- Community interest in predictive genetic testing for susceptibility to major depressive disorder in a large national sample (2010) (36)
- Issues concerning feedback about genetic testing and risk of depression (2009) (36)
- Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophrenia (2005) (36)
- Altered potassium channel function in the superficial dorsal horn of the spastic mouse (2007) (35)
- The association between the oxytocin receptor gene (OXTR) and hypnotizability (2013) (35)
- Heritable mutations in the glycine, GABAA, and nicotinic acetylcholine receptors provide new insights into the ligand-gated ion channel receptor superfamily. (1998) (35)
- Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group (2018) (35)
- Predicting sporadic Alzheimer’s disease progression via inherited Alzheimer’s disease-informed machine-learning (2020) (35)
- Coregulation of genes in the mouse brain following treatment with clozapine, haloperidol, or olanzapine implicates altered potassium channel subunit expression in the mechanism of antipsychotic drug action (2008) (35)
- An examination of multiple classes of rare variants in extended families with bipolar disorder (2018) (34)
- Predictive and diagnostic genetic testing in psychiatry. (2010) (34)
- Localization of the adenosine A1 receptor subtype gene (ADORA1) to chromosome 1q32.1. (1995) (33)
- Intraneuronal advanced glycation endproducts in presenilin‐1 Alzheimer's disease (2002) (33)
- Predicted structure of the extracellular region of ligand‐gated ion‐channel receptors shows SH2‐like and SH3‐like domains forming the ligand‐binding site (1997) (33)
- Probing glycine receptor stoichiometry in superficial dorsal horn neurones using the spasmodic mouse (2011) (33)
- A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26 (2009) (33)
- The contribution of proline 250 (P-2′) to pore diameter and ion selectivity in the human glycine receptor channel (2003) (32)
- A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers (2018) (30)
- Primary structure of the human beta-adrenergic receptor gene. (1987) (30)
- Bovine myoclonus: Model of human hyperekplexia (Startle disease) (2002) (30)
- Clinical, pathophysiological and genetic features of motor symptoms in autosomal dominant Alzheimer's disease. (2019) (30)
- Integrating objective gene-brain-behavior markers of psychiatric disorders. (2007) (30)
- A mutation in codon 717 of the amyloid precursor protein gene in an Australian family with Alzheimer's disease (1995) (30)
- Similar early clinical presentations in familial and non-familial frontotemporal dementia (2004) (30)
- Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (2017) (29)
- Hemorrhage is uncommon in new Alzheimer family with Flemish amyloid precursor protein mutation (2004) (28)
- Characterisation of Genetic Variation in ST8SIA2 and Its Interaction Region in NCAM1 in Patients with Bipolar Disorder (2014) (28)
- Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide (2017) (28)
- Genetic variants associated with longitudinal changes in brain structure across the lifespan (2021) (27)
- Neurological Manifestations of Autosomal Dominant Alzheimer’s Disease from the DIAN cohort and a meta-analysis (2016) (27)
- Altered gene expression in mice treated with the mood stabilizer sodium valproate. (2006) (27)
- The extracellular disulfide loop motif of the inhibitory glycine receptor does not form the agonist binding site. (1993) (27)
- Presymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial magnetic resonance imaging study (2017) (27)
- Ymer, S. et al. Structural and functional characterization of the 1 subunit of GABAA/benzodiazepine receptors. EMBO J. 9, 3261−3267 (1990) (27)
- Host-specific nodulation is encoded on a 14kb DNA fragment in Rhizobium trifolii (2004) (26)
- Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium (2018) (26)
- Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium (2018) (26)
- Cerebral amyloidosis associated with cognitive decline in autosomal dominant Alzheimer disease (2015) (26)
- Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume (2018) (26)
- Investigation of MCPH1 G37995C and ASPM A44871G polymorphisms and brain size in a healthy cohort (2007) (26)
- Genetics of ageing-related changes in brain white matter integrity – A review (2013) (25)
- Structure‐Function Relationships of the Human Glycine Receptor: Insights from Hyperekplexia Mutations (1999) (25)
- A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood (2018) (25)
- Rhizobium nodulation genes involved in root hair curling (Hac) are functionally conserved (1985) (25)
- Carrier-bound odorant delivery to olfactory receptors (1988) (24)
- Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting (2019) (24)
- BDNF Genotype Interacts with Motor Function to Influence Rehabilitation Responsiveness Poststroke (2016) (24)
- Diurnal cortisol variation and cortisol response to an MRI stressor in schizophrenia and bipolar disorder (2016) (24)
- Two-Dimensional Genome Scan Identifies Multiple Genetic Interactions in Bipolar Affective Disorder (2010) (24)
- Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder (2018) (24)
- Anion-cation permeability correlates with hydrated counterion size in glycine receptor channels. (2008) (23)
- Seizures as an early symptom of autosomal dominant Alzheimer's disease (2019) (23)
- Molecular and genetic insights into ligand binding and signal transduction at the inhibitory glycine receptor. (1996) (23)
- Frontotemporal dementia–amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1–q12.2: genetic, clinical and neuropathological analysis (2013) (23)
- Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders (2018) (23)
- Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis? (2015) (22)
- Sequence of Alzheimer disease biomarker changes in cognitively normal adults (2020) (22)
- Association between the serotonin 2A receptor gene and bipolar affective disorder in an Australian cohort (2009) (22)
- Starch swelling power and amylose content of triticale and Triticum timopheevii germplasm (2009) (22)
- Mutations in the glycine receptor α1 subunit (GLRA1) gene in hereditary hyperekplexia pedigrees: evidence for non-penetrance of mutation Y279C (2001) (21)
- Genetic refinement and physical mapping of a 2.3 Mb probable disease region associated with a bipolar affective disorder susceptibility locus on chromosome 4q35 (2003) (21)
- A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19 (2002) (21)
- Effect of BDNFVal66Met on disease markers in dominantly inherited Alzheimer's disease (2018) (21)
- Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders (2021) (21)
- Neuronal fiber bundle lengths in healthy adult carriers of the ApoE4 allele: A quantitative tractography DTI study (2013) (21)
- Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder (2016) (20)
- Association of Longitudinal Changes in Cerebrospinal Fluid Total Tau and Phosphorylated Tau 181 and Brain Atrophy With Disease Progression in Patients With Alzheimer Disease (2019) (20)
- Association between body mass index and subcortical brain volumes in bipolar disorders–ENIGMA study in 2735 individuals (2021) (20)
- Nodulation of specific legumes is controlled by several distinct loci in Rhizobium trifolii (1986) (20)
- 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans (2021) (20)
- A molecular linkage map of nitrogenase and nodulation genes in Rhizobium trifolii (1983) (19)
- Association of SORL1 gene variants with hippocampal and cerebral atrophy and Alzheimer's disease. (2014) (19)
- Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study (2018) (19)
- Attenuated glycine receptor function reduces excitability of mouse medial vestibular nucleus neurons (2010) (19)
- Pore Structure of the Cys-loop Ligand-gated Ion Channels (2009) (19)
- Sequence and expression of a novel GABAA receptor alpha subunit. (1989) (18)
- Localization of the adenosine A2b receptor subtype gene (ADORA2B) to chromosome 17p11.2-p12 by FISH and PCR screening of somatic cell hybrids. (1995) (18)
- Localization of the glycine receptor α1 subunit gene (GLRA1) to chromosome 5q32 by FISH (1994) (17)
- Genetics of Microstructure of the Corpus Callosum in Older Adults (2014) (17)
- Comparison of CSF biomarkers in Down syndrome and autosomal dominant Alzheimer's disease: a cross-sectional study (2021) (17)
- Variant-dependent heterogeneity in amyloid β burden in autosomal dominant Alzheimer's disease: cross-sectional and longitudinal analyses of an observational study (2022) (17)
- Biphasic cortical macro‐ and microstructural changes in autosomal dominant Alzheimer's disease (2020) (17)
- Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs (2021) (16)
- Intrinsic and synaptic homeostatic plasticity in motoneurons from mice with glycine receptor mutations. (2014) (16)
- Dynamics of Brain Structure and its Genetic Architecture over the Lifespan (2020) (16)
- IMPLICATIONS OF THE USE OF GENETIC TESTS IN PSYCHIATRY, WITH A FOCUS ON MAJOR DEPRESSIVE DISORDER: A REVIEW (2013) (16)
- Erratum to “Preclinical trials in autosomal dominant AD: Implementation of the DIAN-TU trial” [Rev. Neurol. 169 (10) (2013) 737–743] (2013) (16)
- Renin-angiotensin system genetic polymorphisms and brain white matter lesions in older Australians. (2014) (15)
- Investigating the Genetics of Hippocampal Volume in Older Adults without Dementia (2015) (15)
- Sequence and expression of human GABAA receptor alpha 1 and beta 1 subunits. (1989) (15)
- Genetics of hand grip strength in mid to late life (2015) (15)
- Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. (2018) (15)
- Australian Brain Alliance (2016) (15)
- Attitudes of medical genetics practitioners and psychiatrists toward communicating with patients about genetic risk for psychiatric disorders (2014) (15)
- PARK2 mutations and clinical features in a Chinese population with early-onset Parkinson’s disease (2008) (15)
- [Accepted Manuscript] Presymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial MRI study. (2017) (15)
- The shared and unique genetic relationship between mental well-being, depression and anxiety symptoms and cognitive function in healthy twins (2017) (14)
- Exploration of experiences with and understanding of polygenic risk scores for bipolar disorder. (2020) (14)
- Raloxifene increases prefrontal activity during emotional inhibition in schizophrenia based on estrogen receptor genotype (2016) (14)
- Genetic correlations between wellbeing, depression and anxiety symptoms and behavioral responses to the emotional faces task in healthy twins (2018) (14)
- Conservation of nif- and species-specific domains within repeated promoter sequences from fast-growing Rhizobium species. (1985) (13)
- Predictive and diagnostic genetic testing in psychiatry. (2010) (13)
- Diverse phenotypic measurements of wellbeing: Heritability, temporal stability and the variance explained by polygenic scores (2020) (13)
- Common polymorphisms in dopamine-related genes combine to produce a ‘schizophrenia-like' prefrontal hypoactivity (2014) (13)
- Exclusion of linkage between bipolar affective disorder and chromosome 16 in 12 Australian pedigrees. (1997) (12)
- Combining schizophrenia and depression polygenic risk scores improves the genetic prediction of lithium response in bipolar disorder patients (2021) (12)
- A negative association between brainstem pontine grey-matter volume, well-being and resilience in healthy twins. (2018) (12)
- Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360) (2017) (12)
- Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. (2016) (12)
- Is CHCHD 10 Pro 34 Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis ? (2015) (12)
- Vulnerability of white matter tracts and cognition to the SOD2 polymorphism: A preliminary study of antioxidant defense genes in brain aging (2017) (12)
- Intelligence, educational attainment, and brain structure in those at familial high‐risk for schizophrenia or bipolar disorder (2020) (12)
- A transcript map encompassing a susceptibility locus for bipolar affective disorder on chromosome 4q35 (2002) (11)
- Endogenous progesterone levels and frontotemporal dementia: modulation of TDP-43 and Tau levels in vitro and treatment of the A315T TARDBP mouse model (2013) (11)
- Autosomal dominantly inherited alzheimer disease: Analysis of genetic subgroups by machine learning (2020) (11)
- Investigating the influence of KIBRA and CLSTN2 genetic polymorphisms on cross-sectional and longitudinal measures of memory performance and hippocampal volume in older individuals (2015) (11)
- Modeling autosomal dominant Alzheimer's disease with machine learning (2021) (11)
- Association between serotonin transporter promoter polymorphisms and psychological distress in a diabetic population (2012) (11)
- Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes. (2020) (11)
- A Neuroethics Framework for the Australian Brain Initiative (2019) (10)
- Preferences Regarding Targeted Education and Risk Assessment in People with a Family History of Major Depressive Disorder (2014) (10)
- Organisation of nodulation and nitrogen fixation genes on a Rhizobium trifolii symbiotic plasmid (1984) (10)
- Molecular pharmacology and drug action: structural information casts light on ligand binding. (1989) (10)
- Impact of the AGTR1 A1166C polymorphism on subcortical hyperintensities and cognition in healthy older adults (2014) (10)
- Neuromarkers of the common angiotensinogen polymorphism in healthy older adults: A comprehensive assessment of white matter integrity and cognition (2016) (10)
- Community attitudes to genetic susceptibility-based mental health interventions for healthy people in a large national sample. (2011) (9)
- Resting-State Functional Connectivity Disruption as a Pathological Biomarker in Autosomal Dominant Alzheimer Disease (2021) (9)
- The role of glycine and glycine receptors in myoclonus and startle syndromes. (2002) (9)
- GSK3B and MAPT Polymorphisms Are Associated with Grey Matter and Intracranial Volume in Healthy Individuals (2013) (9)
- Human Embryonic Stem Cell Research: An Australian Perspective (2007) (9)
- A Western Australian kindred with Dutch cerebral amyloid angiopathy (2005) (9)
- De Novo Gene Variants and Familial Bipolar Disorder (2020) (9)
- Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders (2017) (9)
- Genetic and environmental determinants of variation in the plasma lipidome of older Australian twins (2020) (9)
- Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders (2020) (8)
- Correction: Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals (2019) (8)
- Longitudinal Accumulation of Cerebral Microhemorrhages in Dominantly Inherited Alzheimer Disease (2021) (8)
- Relationships between big‐five personality factors and Alzheimer's disease pathology in autosomal dominant Alzheimer's disease (2020) (8)
- Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes (2021) (8)
- Single-subject grey matter network trajectories over the disease course of autosomal dominant Alzheimer’s disease (2020) (8)
- Does perfectionism in bipolar disorder pedigrees mediate associations between anxiety/stress and mood symptoms? (2017) (8)
- Kv channel interacting protein 3 expression and regulation by haloperidol in midbrain dopaminergic neurons (2009) (8)
- Comparing cortical signatures of atrophy between late-onset and autosomal dominant Alzheimer disease (2020) (8)
- Effect of Fluvoxamine on Amyloid-β Peptide Generation and Memory. (2018) (8)
- Molecular Cloning and Organisation of Genes Involved in Symbiotic Nitrogen Fixation in Different Rhizobium Species (1984) (7)
- Species-specific, symbiotic plasmid-located repeated DNA sequences in Rhizobium trifolii (1985) (7)
- Identification of Sialyltransferase 8 B as a Generalized Susceptibility Gene for Psychotic and Mood Disorders on Chromosome 15 q 25-26 (2012) (7)
- Electroencephalography profiles as a biomarker of wellbeing: A twin study. (2020) (7)
- A cluster randomized controlled trial of an online psychoeducational intervention for people with a family history of depression (2019) (7)
- CHAPTER 21 – Inhibitory Ligand-Gated Ion Channel Receptors: Molecular Biology and Pharmacology of GABAA and Glycine Receptors (1994) (7)
- Baculoviruses expressing the human familial Alzheimer's disease presenilin 1 mutation lacking exon 9 increase levels of an amyloid beta-like protein in Sf9 cells (2004) (7)
- Characterisation of age and polarity at onset in bipolar disorder (2021) (7)
- Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (2019) (7)
- Prediction of lithium response using genomic data (2021) (6)
- Localization of the glycine receptor alpha 1 subunit gene (GLRA1) to chromosome 5q32 by FISH. (1994) (6)
- Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach (2022) (6)
- Exceptional Longevity and Polygenic Risk for Cardiovascular Health (2019) (6)
- Correction: Quantitative Amyloid Imaging in Autosomal Dominant Alzheimer’s Disease: Results from the DIAN Study Group (2016) (6)
- Cluster randomized controlled trial of a psycho-educational intervention for people with a family history of depression for use in general practice (2013) (6)
- Alzheimer Amyloid Precursor Aspartyl Proteinase Activity in CHAPSO Homogenates of Spodoptera frugiperda Cells (2004) (6)
- Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011) (2011) (6)
- Association of BDNF Val66Met With Tau Hyperphosphorylation and Cognition in Dominantly Inherited Alzheimer Disease. (2022) (6)
- Differential effect of disease-associated ST8SIA2 haplotype on cerebral white matter diffusion properties in schizophrenia and healthy controls (2018) (6)
- Autosomal dominant and sporadic late onset Alzheimer disease share a common in vivo pathophysiology. (2022) (6)
- Exploring Culture-Specific Differences in Beliefs about Causes, Kinship and the Heritability of Major Depressive Disorder: The Views of Anglo-Celtic and Chinese-Australians (2013) (5)
- Circular RNA detection identifies circPSEN1 alterations in brain specific to autosomal dominant Alzheimer's disease (2022) (5)
- Plant-Secreted Factors Induce The Expression of R.Trifolii Nodulation and Host-Range Genes (1985) (5)
- Association analysis of transcripts from the bipolar susceptibility locus on chromosome 4q35, exclusion of a pathogenic role for eight positional candidate genes (2005) (5)
- Genome screen of 15 Australian bipolar affective disorder pedigrees supports previously identified loci for bipolar susceptibility genes (2008) (5)
- Parental sex effects in bipolar affective disorder pedigrees (1997) (5)
- Psychosocial implications of living with familial risk of a psychiatric disorder and attitudes to psychiatric genetic testing: A systematic review of the literature (2020) (5)
- Plasma Amyloid-Beta Levels in a Pre-Symptomatic Dutch-Type Hereditary Cerebral Amyloid Angiopathy Pedigree: A Cross-Sectional and Longitudinal Investigation (2021) (5)
- A Psycho-Educational Intervention for People with a Family History of Depression: Pilot Results (2017) (5)
- DBH −1021C>T and COMT Val108/158Met genotype are not associated with the P300 ERP in an auditory oddball task (2013) (5)
- Triallelic relationships between the serotonin transporter polymorphism and cognition among healthy older adults (2014) (5)
- Variable presentation of Alzheimer's disease and/or spastic paraparesis phenotypes in pedigrees with a novel PS-1 exon 9 gene deletion or exon 9 splice acceptor mutations (2000) (5)
- Cortical mediation of relationships between dopamine receptor D2 and cognition is absent in youth at risk of bipolar disorder (2021) (5)
- HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders (2021) (4)
- Propping Mapping of the human adenosine A 2 a receptor gene : relationship to potential schizophrenia loci on chromosome 22 q and exclusion from the CATCH 22 region (4)
- The impact of online brain training exercises on experiences of depression, anxiety and emotional wellbeing in a twin sample. (2020) (4)
- Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification (2013) (4)
- Erratum: Early behavioural changes in familial Alzheimers disease in the Dominantly Inherited Alzheimer Network (Brain (2015) 138 (103645) (10.1093/brain/awv004)) (2015) (4)
- Presymptomatic Dutch-Type Hereditary Cerebral Amyloid Angiopathy-Related Blood Metabolite Alterations. (2020) (4)
- Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis (2020) (3)
- Decreased secretion of amyloid precursor protein in Chinese hamster ovary cells overexpressing presenilin 1 (1999) (3)
- Antibodies as a breeding aid in the production of novel designer wheats with unique health attributes (2008) (3)
- Association of Attention-Deficit/Hyperactivity Disorder and Depression Polygenic Scores with Lithium Response: A Consortium for Lithium Genetics Study (2021) (3)
- No association of spastic paraparesis genes in PSEN1 Alzheimer's disease with spastic paraparesis (2007) (3)
- Rhizobium Trifolii Nodulation and Nitrogen Fixation Genes - A Genetic and Molecular Characterization (1984) (3)
- Neuroimaging within the Dominantly Inherited Alzheimer’s Network (DIAN): PET and MRI (2022) (3)
- A novel hardness-related and starch granule-associated protein marker in wheat: LMW-GS-‘S’ (2012) (3)
- Genetic markers of cholesterol transport and gray matter diffusion: a preliminary study of the CETP I405V polymorphism (2015) (3)
- Biological Activities of Recombinant Human Follicle Stimulating Hormone (1992) (3)
- A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21 (2021) (3)
- Techniques for the Identification of Genes Involved in Psychiatric Disorders (2005) (3)
- Diagnosis of bipolar disorders and body mass index predict clustering based on similarities in cortical thickness—ENIGMA study in 2436 individuals (2021) (3)
- A transient hyperekplexia phenotype associated with compound heterozygote mutations in the human beta-subunit of the inhibitory glycine receptor (GLRB). (2000) (2)
- Imaging and genetic studies in youth at high risk for bipolar disorder (2013) (2)
- ARE WHITE MATTER HYPERINTENSITIES A CORE FEATURE OF ALZHEIMER’S DISEASE OR JUST A REFLECTION OF AMYLOID ANGIOPATHY? EVIDENCE FROM THE DOMINANTLY INHERITED ALZHEIMER NETWORK (DIAN) (2016) (2)
- Physiologically generated presenilin 1 lacking exon 8 fails to rescue brain PS1−/− phenotype and forms complexes with wildtype PS1 and nicastrin (2015) (2)
- A Neuroethics Framework for the Australian Brain Initiative (2020) (2)
- Molecular Anatomy of the Symbiotic Region in Rhizobium trifolii and Rhizobium parasponia (1983) (2)
- Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities (2019) (2)
- Alzheimer’s disease research progress in Australia: The Alzheimer’s Association International Conference Satellite Symposium in Sydney (2021) (2)
- Identification, characterization, and association analysis of novel genes from the bipolar disorder susceptibility locus on chromosome 4q35 (2005) (2)
- Covariance-based vs. correlation-based functional connectivity dissociates healthy aging from Alzheimer disease (2022) (2)
- LONGITUDINAL BIOMARKER CHANGES IN AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE FROM THE DIAN STUDY (2017) (2)
- Different rates of cognitive decline in autosomal dominant and late‐onset Alzheimer disease (2021) (2)
- Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (2018) (2)
- Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning (2022) (2)
- Nonlinkage of D6S260, a putative schizophrenia locus, to bipolar affective disorder. (1996) (2)
- High polygenic risk score for exceptional longevity is associated with a healthy metabolic profile (2022) (2)
- Planar cell polarity pathway and development of the human visual cortex (2018) (2)
- Djinn Lite: a tool for customised gene transcript modelling, annotation-data enrichment and exploration (2006) (2)
- Conservation of Root Hair Curling (HAC) Functions in Fast-Growing Rhizobia (1984) (2)
- Major leads in the search for susceptibility genes for depression (2003) (1)
- Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume (2018) (1)
- Diimidazo[1,2-c:4',5'-e]pyrimidines: adenosine agonist activity demonstrated by microphysiometry. (1998) (1)
- Immune-related genetic enrichment in frontotemporal dementia (2017) (1)
- Genetic architecture of subcortical brain structures in 38,851 individuals (2019) (1)
- Pattern and implications of neurological examination findings in autosomal dominant Alzheimer disease (2022) (1)
- Investigating Olfactory Gene Variation and Odour Identification in Older Adults (2021) (1)
- CSF Tau phosphorylation at Thr205 is associated with loss of white matter integrity in autosomal dominant Alzheimer disease (2022) (1)
- White matter hyperintensities and the mediating role of cerebral amyloid angiopathy in dominantlyinherited Alzheimer’s disease (2018) (1)
- Circular RNA detection identifies circPSEN1 alterations in brain specific to autosomal dominant Alzheimer's disease (2021) (1)
- Polygenic scores for major depressive disorder and depressive symptoms predict response to lithium in patients with bipolar disorder (2018) (1)
- GENOTYPIC VARIANCE MAY EXPLAIN THE BALANCE OF EARLY CORTICAL VERSUS STRIATAL AMYLOID DEPOSITION IN AUTOSOMAL DOMINANT AD (2017) (1)
- High genetic loading of schizophrenia predicts poor response to lithium in patients with bipolar disorder: A polygenic score and cross-trait genetic analysis (2017) (1)
- A genetic and molecular analysis of the nodulation genes of rhizobium trifolii (1984) (1)
- Comment: The Epidemiology of the Genetic Liability for Schizophrenia (2000) (1)
- Memory in Neurodegenerative Disease: Biological and psychosocial risk factors for dementia and memory loss (1998) (1)
- Pattern and degree of individual brain atrophy predicts dementia onset in dominantly inherited Alzheimer's disease (2021) (1)
- Analysis of a bipolar affective disorder susceptibility locus on chromosome 4q35 (2000) (1)
- across RNA cell death gene networks is implicated in the semantic variant of primary progressive aphasia. (2019) (1)
- Characterization of Age and Polarity at Onset in Bipolar Disorder (2021) (1)
- Functional expression inXenopusoocytesofthe strychnine binding 48kdsubunit oftheglycine receptor (1989) (1)
- Coregulation of genes in the mouse brain following antipsychotic drug treatment (2006) (1)
- Brain network decoupling with increased serum neurofilament and reduced cognitive function in Alzheimer's disease. (2023) (1)
- Familial Alzheimer’s disease in Australia (2020) (1)
- Plasma glial fibrillary acidic protein in autosomal dominant Alzheimer's disease: Associations with Aβ-PET, neurodegeneration, and cognition. (2022) (1)
- Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia (2019) (1)
- P1-217 Beta amyloid toxicity in Alzheimer's disease (2004) (1)
- Dementia Incidence, APOE Genotype, and Risk Factors for Cognitive Decline in Aboriginal Australians (2022) (1)
- HABITUAL EXERCISE LEVELS ARE ASSOCIATED WITH CEREBRAL AMYLOID LOAD IN PRE-SYMPTOMATIC AUTOSOMAL DOMINANT ALZHEIMER’S DISEASE (2017) (0)
- Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer’s disease (2019) (0)
- White matter hyperintensities and the mediating role of cerebral amyloid angiopathy in dominantly-inherited Alzheimerâ•Žs disease (2019) (0)
- CHAPTER H4 – Bovine Hyperekplexia (2005) (0)
- A Novel Engineered Single-Chain Antibody Fragment for Targeting Pediatric Philadelphia Chromosome-like Acute Lymphoblastic Leukemia (2020) (0)
- Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (2020) (0)
- SA29 ADDRESSING THE IMPACT OF RARE GENETIC VARIANTS IN EXTENDED/MULTIPLEX BIPOLAR FAMILIES (2019) (0)
- Effect of BDNFVal66Met on disease markers in dominantly inherited AD (2018) (0)
- The TWIN-E project: identifying risk and resilience gene-brain markers of emotional well-being (2012) (0)
- MRI results from the DIAN study The pattern of atrophy in familial Alzheimer disease : Volumetric (0)
- Symposium Biology of ligand-gated ion channels (1997) (0)
- Cellular Expression of Cloned and Mutated Ion Channels (2019) (0)
- Identification Of A novel FTD-MND gene on chromosome 16 (2016) (0)
- SIGMAR1 Association Analysis With Dementia And Parkinsonism Phenotypes (2009) (0)
- P3-312 Functional consequences of tau haplotype and subhaplotypes in human brains (2006) (0)
- Biological activity and metabolic clearance of recombinant human follicle stimulating hormone produced in Sp2/0 myeloma cells (1996) (0)
- Clinical Importance of Paraganglioma Genetics (2005) (0)
- Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach – CORRIGENDUM (2022) (0)
- Prediction of lithium response using genomic data (2021) (0)
- Reply to García‐Gorostiaga, et al. (2009) (0)
- A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19 (2004) (0)
- Erratum: A Neuroethics Framework for the Australian Brain Initiative (Neuron (2019) 101(3) (365–369), (S0896627319300054), (10.1016/j.neuron.2019.01.004)) (2020) (0)
- Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia (2019) (0)
- Physical activity, cognition, and Alzheimer pathology in autosomal dominant Alzheimer`s disease (2018) (0)
- P1-332 Glycogen synthase kinase -3 beta polymorphisms interact with Tau haplotypes in Alzheimer’s disease (2006) (0)
- ADDRESSING RARE VARIANT CONTRIBUTIONS TO THE GENETIC ARCHITECTURE OF BIPOLAR DISORDER, UTILIZING EXTENDED FAMILIES WITH HIGHLY PENETRANT FORMS OF ILLNESS (2017) (0)
- Herpes simplex virus and rates of cognitive decline or whole brain atrophy in the Dominantly Inherited Alzheimer Network (2022) (0)
- Higher systolic blood pressure in early-mid adulthood is associated with poorer cognitive performance in those with a dominantly inherited Alzheimer's disease mutation but not in non-carriers. Results from the DIAN study. (2023) (0)
- Perceptions of Predictive Genetic Testing Measure (2014) (0)
- Axonal damage and astrocytosis are biological correlates of grey matter network integrity loss: a cohort study in autosomal dominant Alzheimer disease (2023) (0)
- Molecular studies of synaptic neurotran fission: Development of transgenic animal models (1999) (0)
- Positional cloning identifies SIGMAR1 gene as a causative locus for FTLD-MND in a large Australian pedigree (2011) (0)
- P4-087 Familial Alzheimer's disease and cerebral haemorrhage: a second family with the flemish APP ALA692GLY mutation (2004) (0)
- The role of depolarising and repolarising currents in the induction of early afterdepolarisations during acute hypoxia in ventricular myocytes (2008) (0)
- The NARF symposium - Australian Advances in Alzheimers Research (1998) (0)
- Mega-analysis of association between obesity and cortical morphology in bipolar disorders: ENIGMA study in 2832 participants. (2023) (0)
- SORL1 gene variants are associated with brain white matter hyperintensities and dementia (2010) (0)
- Compositions and methods for synthesis and analysis of enkephalinase. (1987) (0)
- SA39 A CLUSTER RANDOMIZED CONTROLLED TRIAL OF A PSYCHOEDUCATIONAL INTERVENTION FOR PEOPLE WITH A FAMILY HISTORY OF DEPRESSION FOR USE IN GENERAL PRACTICE (2019) (0)
- P1-318 A novel Alzheimer’s disease locus associated with atypical ‘plaque-predominant’ neuropathology (2006) (0)
- AD‐causing variants that affect PSEN1 transmembrane domains are associated with faster neurodegeneration and cognitive decline compared to those affecting cytoplasmic domains. (2022) (0)
- Successful ageing in older adults with intellectual disabilities: predictors and correlates of cognitive decline (2013) (0)
- A soluble phosphorylated tau signature links tau, amyloid and the evolution of stages of dominantly inherited Alzheimer’s disease (2020) (0)
- THE DEVELOPING BRAIN DEVELOPING PSYCHOPATHOLOGY (2017) (0)
- Functional Characterisation of Mirna Implicated in Psychiatric Syndromes (2017) (0)
- Identification of a bipolar disorder susceptibility locus on chromosome 15Q (2006) (0)
- Age related changes in heritability of white matter (2013) (0)
- 118.4 Diurnal Cortisol Variation and Cortisol Response to an MRI Stressor in Schizophrenia and Bipolar Disorder (2017) (0)
- Investigation of circadian disruption in bipolar disorder (2006) (0)
- The genetics of familial dementias (2009) (0)
- Presenilin 1 mutations in Australian Alzheimer's Disease pedigrees and their role in altering APP metabolism (1997) (0)
- Purification and Characterization of Recombinant Human Follicle Stimulating Hormone (1992) (0)
- MOTOR SYMPTOMS IN FAMILIAL ALZHEIMER’S DISEASE: FREQUENCY, SEVERITY AND PREDICTIVE VALUE (2017) (0)
- M49 EPIGENOME-WIDE ASSOCIATION STUDY (EWAS) OF YOUNG PEOPLE WITH FAMILIAL RISK OF BIPOLAR DISORDER (2019) (0)
- forming the ligand-binding site ion-channel receptors shows SH 2-like and SH 3-like domains Predicted structure of the extracellular region of ligand-gated (2002) (0)
- INCREASED FREQUENCY OF NOVEL NRG1 GENE VARIANTS IN SCHIZOPHRENIA AND THE EFFECT OF NUCLEOTIDE VARIATION ON MRNA ISOFORM TRANSCRIPTIONAL REGULATION (2010) (0)
- VKučinskas-2001-2016 (2016) (0)
- Author response: Bundle-specific associations between white matter microstructure and Aβ and tau pathology in preclinical Alzheimer’s disease (2021) (0)
- Factors influencing the decision to learn 5-HTT genotype results and subsequent impact on the individual (2006) (0)
- University of Groningen Brain Aging in Major Depressive Disorder: Results from the ENIGMA Major Depressive Disorder working group ‘for the ENIGMA-MDD Consortium’; Han, (2019) (0)
- PDGF Receptor Alpha Inhibition Prevents High Blood Flow-induced Atherosclerotic Plaque Regression (2018) (0)
- Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 (2016) (0)
- Comparison of amyloid accumulation between Down syndrome and autosomal‐dominant Alzheimer disease (2022) (0)
- The location of PSEN1 pathogenic variants in transmembrane vs. cytoplasmic domains may alter neurodegenerative and cognitive trajectories: Findings from the DIAN study (2021) (0)
- What now for Alzheimer's disease? An epidemiological evaluation of the AD2000 trial (2005) (0)
- Cover Image, Volume 186B, Number 8, December 2021 (2021) (0)
- AD‐causing variants that affect PSEN1 transmembrane domains are associated with faster neurodegeneration and cognitive decline compared to those affecting cytoplasmic domains (2022) (0)
- Channel gating in the LGIC receptor superfamily – insights into the signal: Recent papers on ligand-gated ion channels reveal more molecular detail on the conformational changes that follow ligand binding and lead to pore opening (2005) (0)
- P-18-15 Linkage analyses of chromosomes 6 (pter-p22), 16, 18 (pericentromeric) and 21 (q22.3) in bipolar disorder pedigrees (1996) (0)
- Identification and analysis of candidate genes from the bipolar disorder susceptibility locus on chromosome 4q35 (2004) (0)
- A negative association between brainstem pontine grey-matter volume, well-being and resilience in healthy twins (2018) (0)
- Change in cerebrospinal fluid tau microtubule binding region detects symptom onset, cognitive decline, tangles, and atrophy in Dominantly Inherited Alzheimer's Disease. (2023) (0)
- Biomarker clustering in autosomal dominant Alzheimer's disease (2022) (0)
- First presentation with neuropsychiatric symptoms in autosomal dominant Alzheimer’s disease: the Dominantly Inherited Alzheimer’s Network Study (2022) (0)
- PREDICTING CONVERSION TO BIPOLAR DISORDER IN A PROSPECTIVE LONGITUDINAL GENETICALLY HIGH-RISK SAMPLE (2017) (0)
- 417: A consanguineous family with Frontotemporal Dementia/Motor Neuron Disease (2008) (0)
- Altered inhibitory synaptic transmission in superficial dorsal horn neurones in spastic and oscillator mice (2003) (0)
- AuPS/ASB Meeting-Newcastle 2007 Free communications: Ion channels (2007) (0)
- Schizophrenia and Cognitive Dysfunction Associated with the Estrogen Receptor 1 Genotype (2016) (0)
- Stress Sampler I: psychosocial adjustment and psychiatric and physical comorbidity in diabetes mellitus (2006) (0)
- Comparison of amyloid accumulation between Down syndrome and autosomal‐dominant Alzheimer disease (2022) (0)
- Table of Contents (1995) (0)
- Selective errors in declarative memory and hippocampal function associated with brain derived neurotrophic factor polymorphism (2005) (0)
- Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia (2018) (0)
- Positional cloning, association analysis, and expression studies provide convergent evidence that the cadherin gene fat contains a bipolar disorder susceptibility allele (2005) (0)
- LONGITUDINAL CLINICAL AND BIOMARKER CHANGES IN DOMINANTLY INHERITED ALZHEIMER'S DISEASE: THE DOMINANTLY INHERITED ALZHEIMER NETWORK (2016) (0)
- C59 DIVERSE ETIOLOGIES AND CONVERGENCE OF PATHOLOGY IN ALS (2011) (0)
- CSF Biomarkers in Down Syndrome and Autosomal Dominant Alzheimer Disease (2021) (0)
- Environmental modulation of phenotype in neuregulin 1 mutants (2008) (0)
- Erratum: Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific reports (2017) 7 1 (8899)) (2018) (0)
- M68 THE RELATIONSHIP BETWEEN FUNCTIONAL DOPAMINE D2 RECEPTOR HAPLOTYPES AND COGNITIVE OUTCOMES, AS MEDIATED BY REGIONAL BRAIN STRUCTURE: A COMPARISON OF CONTROL, AT-RISK, AND BIPOLAR DISORDER SUBJECTS (2019) (0)
- Haplotype analysis defines a 4.7Mb probable disease region for a bipolar affective disorder susceptibility locus on chromosome 4q35 (2001) (0)
- Stylized transcript map of chromosome 4q35 encompassing the locus for a bipolar disorder susceptibility gene (2002) (0)
This paper list is powered by the following services:
What Schools Are Affiliated With Peter Robert Schofield?
Peter Robert Schofield is affiliated with the following schools:
