# | Title | Journal | Year | Citations |
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1 | Evaluating the comparability of gene expression in blood and brain | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2006 | 512 |
2 | Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2006 | 494 |
3 | Autism spectrum disorders and autistic traits: A decade of new twin studies | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2011 | 475 |
4 | Hypermethylation of the reelin (RELN) promoter in the brain of schizophrenic patients: A preliminary report | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 347 |
5 | Genome‐wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2008 | 335 |
6 | Differential immune system DNA methylation and cytokine regulation in post‐traumatic stress disorder | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2011 | 294 |
7 | Novel de novo SHANK3 mutation in autistic patients | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2009 | 289 |
8 | CAG‐repeat length and the age of onset in Huntington disease (HD): A review and validation study of statistical approaches | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2010 | 289 |
9 | DNA extracted from saliva for methylation studies of psychiatric traits: Evidence tissue specificity and relatedness to brain | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2015 | 281 |
10 | Prevalence of psychiatric disorders in 4 to 16-year-olds with Williams syndrome | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2006 | 256 |
11 | Suggestive evidence for association of the circadian genesPERIOD3andARNTLwith bipolar disorder | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2006 | 254 |
12 | The relationship of 5HTT (SLC6A4) methylation and genotype on mRNA expression and liability to major depression and alcohol dependence in subjects from the Iowa Adoption Studies | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2008 | 254 |
13 | Relationship between dopaminergic neurotransmission, alcoholism, and reward deficiency syndrome | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 248 |
14 | Mutation screening of thePTEN gene in patients with autism spectrum disorders and macrocephaly | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2007 | 248 |
15 | Defining key features of the broad autism phenotype: A comparison across parents of multiple‐ and single‐incidence autism families | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2008 | 245 |
16 | Meta-analysis of the association of a functional serotonin transporter promoter polymorphism with alcohol dependence | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 244 |
17 | Coordinated changes in AHRR methylation in lymphoblasts and pulmonary macrophages from smokers | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2012 | 230 |
18 | 5‐HTTLPR genotype and anxiety‐related personality traits: A meta‐analysis and new data | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2009 | 229 |
19 | Genome‐wide association scan of attention deficit hyperactivity disorder | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2008 | 228 |
20 | The involvement ofErbB4 with schizophrenia: Association and expression studies | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2006 | 226 |
21 | Transcriptional analysis of multiple brain regions in Parkinson's disease supports the involvement of specific protein processing, energy metabolism, and signaling pathways, and suggests novel disease mechanisms | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 220 |
22 | Monoamine oxidase A (MAOA) and antisocial behaviors in the presence of childhood and adolescent maltreatment | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 217 |
23 | Deletions of NRXN1 (neurexin‐1) predispose to a wide spectrum of developmental disorders | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2010 | 217 |
24 | A family study of early-onset obsessive-compulsive disorder | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 215 |
25 | Abnormal elevation ofFMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 215 |
26 | Meta-analysis of the association between two polymorphisms in the serotonin transporter gene and affective disorders | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 214 |
27 | Mood and anxiety disorders in females with the FMR1 premutation | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2009 | 214 |
28 | Methylation at SLC6A4 is linked to family history of child abuse: An examination of the Iowa Adoptee sample | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2010 | 209 |
29 | On the outside, looking in: A review and evaluation of the comparability of blood and brain “‐omes” | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2013 | 208 |
30 | Assessing the validity of blood-based gene expression profiles for the classification of schizophrenia and bipolar disorder: A preliminary report | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 205 |
31 | Genome‐wide association study of schizophrenia in Ashkenazi Jews | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2015 | 203 |
32 | The 3111T/C polymorphism ofhClock is associated with evening preference and delayed sleep timing in a Japanese population sample | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 198 |
33 | Indexing disease progression at study entry with individuals at‐risk for Huntington disease | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2011 | 193 |
34 | Human brain derived neurotrophic factor (BDNF) genes, splicing patterns, and assessments of associations with substance abuse and Parkinson's Disease | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 192 |
35 | Cytogenetic and molecular characterization of A2BP1 / FOX1 as a candidate gene for autism | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2007 | 192 |
36 | Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2009 | 192 |
37 | Familial aggregation of quantitative autistic traits in multiplex versus simplex autism | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2009 | 190 |
38 | Analysis of DRD4 and DAT polymorphisms and behavioral inhibition in healthy adults: Implications for impulsivity | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2008 | 188 |
39 | Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2006 | 187 |
40 | Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2008 | 182 |
41 | Support for association between ADHD and two candidate genes:NET1andDRD1 | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2005 | 180 |
42 | Actimetric evidence that CLOCK 3111 T/C SNP influences sleep and activity patterns in patients affected by bipolar depression | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2007 | 179 |
43 | Convergent functional genomics of genome‐wide association data for bipolar disorder: Comprehensive identification of candidate genes, pathways and mechanisms | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2009 | 178 |
44 | Brain derived neurotrophic factor (BDNF) gene variants and Alzheimer's disease, affective disorders, posttraumatic stress disorder, schizophrenia, and substance dependence | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2006 | 170 |
45 | Sapap3 and pathological grooming in humans: Results from the OCD collaborative genetics study | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2009 | 170 |
46 | Three major haplotypes of the β2 adrenergic receptor define psychological profile, blood pressure, and the risk for development of a common musculoskeletal pain disorder | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2006 | 169 |
47 | Association of the SLC1A1 glutamate transporter gene and obsessive‐compulsive disorder | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2007 | 165 |
48 | Microbiome, inflammation, epigenetic alterations, and mental diseases | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2017 | 165 |
49 | Understanding comorbidity: A twin study of reading disability and attention-deficit/hyperactivity disorder | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2007 | 164 |
50 | Serotonin transporter mRNA levels are associated with the methylation of an upstream CpG island | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2007 | 163 |