Published in Am J Hum Genet on February 05, 2009
Human genetic disorders of axon guidance. Cold Spring Harb Perspect Biol (2010) 1.49
The genetics of colored sequence synesthesia: suggestive evidence of linkage to 16q and genetic heterogeneity for the condition. Behav Brain Res (2011) 1.14
Misophonia: physiological investigations and case descriptions. Front Hum Neurosci (2013) 1.13
Enhanced cortical excitability in grapheme-color synesthesia and its modulation. Curr Biol (2011) 1.02
Pseudo-synesthesia through reading books with colored letters. PLoS One (2012) 0.98
Defining the biological bases of individual differences in musicality. Philos Trans R Soc Lond B Biol Sci (2015) 0.97
Survival of the synesthesia gene: why do people hear colors and taste words? PLoS Biol (2011) 0.96
A longitudinal study of grapheme-color synesthesia in childhood: 6/7 years to 10/11 years. Front Hum Neurosci (2013) 0.94
Grapheme-color synaesthesia is associated with a distinct cognitive style. Front Psychol (2013) 0.94
Why vicarious experience is not an instance of synesthesia. Front Hum Neurosci (2013) 0.92
Absolute pitch exhibits phenotypic and genetic overlap with synesthesia. Hum Mol Genet (2013) 0.92
Mirror-touch and ticker tape experiences in synesthesia. Front Psychol (2013) 0.88
Impaired acquisition of novel grapheme-color correspondences in synesthesia. Front Hum Neurosci (2013) 0.87
What is the link between synaesthesia and sound symbolism? Cognition (2014) 0.84
Adults can be trained to acquire synesthetic experiences. Sci Rep (2014) 0.83
Is synesthesia more common in patients with Asperger syndrome? Front Hum Neurosci (2013) 0.82
Training, hypnosis, and drugs: artificial synaesthesia, or artificial paradises? Front Psychol (2013) 0.82
Serotonergic hyperactivity as a potential factor in developmental, acquired and drug-induced synesthesia. Front Hum Neurosci (2013) 0.81
Combined structural and functional imaging reveals cortical deactivations in grapheme-color synaesthesia. Front Psychol (2013) 0.80
Colored halos around faces and emotion-evoked colors: a new form of synesthesia. Neurocase (2011) 0.80
The effect of listening to music on human transcriptome. PeerJ (2015) 0.80
Defining (trained) grapheme-color synesthesia. Front Hum Neurosci (2014) 0.79
Is synaesthesia more common in autism? Mol Autism (2013) 0.79
Synesthesia, pseudo-synesthesia, and irritable bowel syndrome. Dig Dis Sci (2012) 0.79
Color associations for days and letters across different languages. Front Psychol (2014) 0.79
The Influence of Pathologies upon Sensory Perception and Sensory Coordination in Children with Developmental Dyslexia and Learning Disorders: A Unified Theory of Developmental Dyslexia. N Am J Med Sci (2012) 0.78
The immune hypothesis of synesthesia. Front Hum Neurosci (2013) 0.78
Creative Activities in Music - A Genome-Wide Linkage Analysis. PLoS One (2016) 0.77
Is synaesthesia a dominantly female trait? Cogn Neurosci (2015) 0.77
Training synesthetic letter-color associations by reading in color. J Vis Exp (2014) 0.76
Sensory perception: lessons from synesthesia: using synesthesia to inform the understanding of sensory perception. Yale J Biol Med (2013) 0.76
Do sequence-space synaesthetes have better spatial imagery skills? Yes, but there are individual differences. Cogn Process (2015) 0.76
Grapheme-color synesthesia and posttraumatic stress disorder: preliminary results from the veterans health study. Psychosom Med (2012) 0.76
Convergent evidence for the molecular basis of musical traits. Sci Rep (2016) 0.75
Implicit associative learning in synesthetes and nonsynesthetes. Psychon Bull Rev (2016) 0.75
Mirror-Touch Synaesthesia Is Not Associated with Heightened Empathy, and Can Occur with Autism. PLoS One (2016) 0.75
Absolute Pitch and Synesthesia: Two Sides of the Same Coin? Shared and Distinct Neural Substrates of Music Listening. ICMPC (2012) 0.75
Synesthesia and release phenomena in sensory and motor grounding. Cases of disinhibited embodiment? Front Psychol (2015) 0.75
Atypical sensory sensitivity as a shared feature between synaesthesia and autism. Sci Rep (2017) 0.75
The Emergence of Synaesthesia in a Neuronal Network Model via Changes in Perceptual Sensitivity and Plasticity. PLoS Comput Biol (2016) 0.75
Explicit Associative Learning and Memory in Synesthetes and Nonsynesthetes. Iperception (2016) 0.75
Synesthesia and the McCollough Effect. Iperception (2017) 0.75
Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol (2000) 128.08
Merlin--rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet (2001) 53.16
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet (1995) 49.77
PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet (1998) 23.25
Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet (1997) 13.93
A class of tests for linkage using affected pedigree members. Biometrics (1994) 10.40
Genetic enhancement of learning and memory in mice. Nature (1999) 8.06
Tbr1 regulates differentiation of the preplate and layer 6. Neuron (2001) 5.19
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2. Nat Genet (2000) 5.05
Autism and abnormal development of brain connectivity. J Neurosci (2004) 4.93
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am J Hum Genet (2001) 3.54
On the cellular and network bases of epileptic seizures. Annu Rev Physiol (2001) 3.27
Nuclear translocation and transcription regulation by the membrane-associated guanylate kinase CASK/LIN-2. Nature (2000) 2.74
Eagle-eyed visual acuity: an experimental investigation of enhanced perception in autism. Biol Psychiatry (2008) 2.53
Sodium channels SCN1A, SCN2A and SCN3A in familial autism. Mol Psychiatry (2003) 2.48
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat Genet (2001) 2.48
Increased structural connectivity in grapheme-color synesthesia. Nat Neurosci (2007) 2.46
NMDA receptor-dependent synaptic reinforcement as a crucial process for memory consolidation. Science (2000) 2.37
DCDC2 is associated with reading disability and modulates neuronal development in the brain. Proc Natl Acad Sci U S A (2005) 2.35
Localisation of a gene implicated in a severe speech and language disorder. Nat Genet (1998) 2.33
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet (2006) 2.14
Unconscious priming eliminates automatic binding of colour and alphanumeric form in synaesthesia. Nature (2001) 2.06
Synaesthesia: the prevalence of atypical cross-modal experiences. Perception (2006) 2.06
Functional magnetic resonance imaging of synesthesia: activation of V4/V8 by spoken words. Nat Neurosci (2002) 2.05
Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus. Am J Hum Genet (2001) 2.01
Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nat Genet (2004) 1.98
T-brain-1: a homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex. Neuron (1995) 1.84
The genetic lexicon of dyslexia. Annu Rev Genomics Hum Genet (2007) 1.72
Sound-colour synaesthesia: to what extent does it use cross-modal mechanisms common to us all? Cortex (2006) 1.72
Psychophysical investigations into the neural basis of synaesthesia. Proc Biol Sci (2001) 1.64
Comparative distribution of voltage-gated sodium channel proteins in human brain. Brain Res Mol Brain Res (2001) 1.60
Cortical and thalamic axon pathfinding defects in Tbr1, Gbx2, and Pax6 mutant mice: evidence that cortical and thalamic axons interact and guide each other. J Comp Neurol (2002) 1.56
Non-random associations of graphemes to colours in synaesthetic and non-synaesthetic populations. Cogn Neuropsychol (2005) 1.56
Autism at the beginning: microstructural and growth abnormalities underlying the cognitive and behavioral phenotype of autism. Dev Psychopathol (2005) 1.55
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene. Mol Psychiatry (2003) 1.47
Colored hearing synesthesia: an investigation of neural factors. Neurology (1989) 1.44
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates. BMC Med Genet (2005) 1.44
Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy. Ann Neurol (2004) 1.40
SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum. Epilepsia (2007) 1.40
A family of proteins implicated in axon guidance and outgrowth. J Neurobiol (1999) 1.39
Distribution of voltage-gated sodium channel alpha-subunit and beta-subunit mRNAs in human hippocampal formation, cortex, and cerebellum. J Comp Neurol (2000) 1.34
Evidence for linkage and association with reading disability on 6p21.3-22. Am J Hum Genet (2002) 1.31
Hearing words and seeing colours: an experimental investigation of a case of synaesthesia. Perception (1987) 1.26
Searching for Shereshevskii: what is superior about the memory of synaesthetes? Q J Exp Psychol (Hove) (2007) 1.23
Genetic influences on language impairment and phonological short-term memory. Trends Cogn Sci (2005) 1.22
Familial patterns and the origins of individual differences in synaesthesia. Cognition (2007) 1.20
Diagnosing and phenotyping visual synaesthesia: a preliminary evaluation of the revised test of genuineness (TOG-R). Cortex (2006) 1.17
Aversion, awareness, and attraction: investigating claims of hyperacusis in the Williams syndrome phenotype. J Child Psychol Psychiatry (2005) 1.11
Synaesthesia: prevalence and familiality. Perception (1996) 1.10
Auditory event-related brain potentials in autistic children and three different control groups. Biol Psychiatry (1995) 1.06
Synesthetic color experiences influence memory. Psychol Sci (2002) 1.05
Is synaesthesia an X-linked dominant trait with lethality in males? Perception (2005) 0.98
Ermin, a myelinating oligodendrocyte-specific protein that regulates cell morphology. J Neurosci (2006) 0.97
Autism and cytogenetic abnormalities: solving autism one chromosome at a time. Curr Psychiatry Rep (2007) 0.93
Brief report: assessment of sensory abnormalities in people with autistic spectrum disorders. J Autism Dev Disord (2004) 0.93
Synesthesia and number cognition in children. Cognition (2007) 0.84
HUlip, a human homologue of unc-33-like phosphoprotein of Caenorhabditis elegans; Immunohistochemical localization in the developing human brain and patterns of expression in nervous system tumors. J Neurooncol (2005) 0.84
Cognitive dedifferentiation in eidetics and synaesthesia: hunting for the ghost once more. Perception (1999) 0.77
Functional impact of global rare copy number variation in autism spectrum disorders. Nature (2010) 14.66
Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet (2007) 14.05
A common inversion under selection in Europeans. Nat Genet (2005) 13.66
A common variant associated with prostate cancer in European and African populations. Nat Genet (2006) 13.47
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. Nat Genet (2007) 11.62
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet (2012) 7.59
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nat Genet (2008) 6.97
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat Genet (2008) 6.26
Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas. Nat Genet (2012) 6.25
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. Nat Genet (2007) 6.02
Molecular evolution of FOXP2, a gene involved in speech and language. Nature (2002) 5.89
A functional genetic link between distinct developmental language disorders. N Engl J Med (2008) 4.99
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. Nat Genet (2010) 4.20
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk. Nat Genet (2007) 3.93
Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proc Natl Acad Sci U S A (2004) 3.73
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am J Hum Genet (2005) 3.50
A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet (2010) 3.42
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk. Nat Genet (2012) 3.19
Genetic heterogeneity between the three components of the autism spectrum: a twin study. J Am Acad Child Adolesc Psychiatry (2006) 3.16
Infant neural sensitivity to dynamic eye gaze is associated with later emerging autism. Curr Biol (2012) 3.08
SNP and haplotype mapping for genetic analysis in the rat. Nat Genet (2008) 2.96
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders. PLoS Genet (2012) 2.65
The development of siblings of children with autism at 4 and 14 months: social engagement, communication, and cognition. J Child Psychol Psychiatry (2006) 2.61
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain (2003) 2.55
Eagle-eyed visual acuity: an experimental investigation of enhanced perception in autism. Biol Psychiatry (2008) 2.53
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nat Genet (2001) 2.48
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. PLoS Genet (2011) 2.47
Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Hum Mol Genet (2012) 2.46
Distinctive patterns of microRNA expression associated with karyotype in acute myeloid leukaemia. PLoS One (2008) 2.27
The Autism Spectrum Quotient: Children's Version (AQ-Child). J Autism Dev Disord (2007) 2.24
Predicting language outcome in infants with autism and pervasive developmental disorder. Int J Lang Commun Disord (2003) 2.24
Impaired recognition of social emotions following amygdala damage. J Cogn Neurosci (2002) 2.19
Theory of mind in patients with frontal variant frontotemporal dementia and Alzheimer's disease: theoretical and practical implications. Brain (2002) 2.17
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet (2006) 2.14
A 15q13.3 microdeletion segregating with autism. Eur J Hum Genet (2008) 2.12
Fetal testosterone and autistic traits. Br J Psychol (2008) 2.09
Costs of ABO incompatible living donor transplantation are justified. Transplantation (2006) 2.07
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biol Psychiatry (2010) 2.07
Fetal testosterone influences sexually dimorphic gray matter in the human brain. J Neurosci (2012) 2.05
A behavioral comparison of male and female adults with high functioning autism spectrum conditions. PLoS One (2011) 2.02
Differential activation of the amygdala and the 'social brain' during fearful face-processing in Asperger Syndrome. Neuropsychologia (2006) 2.02
Systemizing empathy: teaching adults with Asperger syndrome or high-functioning autism to recognize complex emotions using interactive multimedia. Dev Psychopathol (2006) 1.96
Visual orienting in the early broader autism phenotype: disengagement and facilitation. J Child Psychol Psychiatry (2009) 1.93
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction. Nat Genet (2013) 1.91
Self-referential cognition and empathy in autism. PLoS One (2007) 1.88
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. Am J Hum Genet (2004) 1.76
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. Sci Transl Med (2010) 1.75
Fetal testosterone and empathy. Horm Behav (2005) 1.74
Atypical neural self-representation in autism. Brain (2009) 1.73
The genetic lexicon of dyslexia. Annu Rev Genomics Hum Genet (2007) 1.72
Neural correlates of eye gaze processing in the infant broader autism phenotype. Biol Psychiatry (2009) 1.71
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. Am J Psychiatry (2008) 1.69
Shared neural circuits for mentalizing about the self and others. J Cogn Neurosci (2010) 1.67
A pilot randomised control trial of a parent training intervention for pre-school children with autism. Preliminary findings and methodological challenges. Eur Child Adolesc Psychiatry (2002) 1.67
Linkage of osteoporosis to chromosome 20p12 and association to BMP2. PLoS Biol (2003) 1.64
The emergence of the social brain network: evidence from typical and atypical development. Dev Psychopathol (2005) 1.64
Functional disconnectivity of the medial temporal lobe in Asperger's syndrome. Biol Psychiatry (2005) 1.64
Fetal testosterone predicts sexually differentiated childhood behavior in girls and in boys. Psychol Sci (2009) 1.64
A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. Am J Hum Genet (2002) 1.63
Fetal testosterone and sex differences. Early Hum Dev (2006) 1.62
Use of multivariate linkage analysis for dissection of a complex cognitive trait. Am J Hum Genet (2003) 1.62
Defining the broader, medium and narrow autism phenotype among parents using the Autism Spectrum Quotient (AQ). Mol Autism (2010) 1.59
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Hum Mutat (2010) 1.59
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nat Genet (2013) 1.59
SNP rs6457327 in the HLA region on chromosome 6p is predictive of the transformation of follicular lymphoma. Blood (2011) 1.57
Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT. Am J Hum Genet (2005) 1.56
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS Genet (2011) 1.56
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia. Blood (2008) 1.56
Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia. Genes Chromosomes Cancer (2008) 1.55
Reduced functional connectivity within and between 'social' resting state networks in autism spectrum conditions. Soc Cogn Affect Neurosci (2012) 1.54
The Autism-Spectrum Quotient (AQ) in Japan: A cross-cultural comparison. J Autism Dev Disord (2006) 1.54
Phenotypic and genetic overlap between autistic traits at the extremes of the general population. J Am Acad Child Adolesc Psychiatry (2006) 1.54
Deciphering the genetic basis of speech and language disorders. Annu Rev Neurosci (2003) 1.53
Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection. Am J Med Genet B Neuropsychiatr Genet (2006) 1.53
Change detection in children with autism: an auditory event-related fMRI study. Neuroimage (2005) 1.52
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. Nat Genet (2012) 1.52
Brain hyper-reactivity to auditory novel targets in children with high-functioning autism. Brain (2008) 1.49
A genomewide linkage screen for relative hand skill in sibling pairs. Am J Hum Genet (2002) 1.46
Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease. Proc Natl Acad Sci U S A (2008) 1.44
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Dev Med Child Neurol (2013) 1.44
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet (2011) 1.43
Impaired recognition of negative basic emotions in autism: a test of the amygdala theory. Soc Neurosci (2006) 1.42
Fetal testosterone and empathy: evidence from the empathy quotient (EQ) and the "reading the mind in the eyes" test. Soc Neurosci (2006) 1.42
The CAST (Childhood Asperger Syndrome Test): test accuracy. Autism (2005) 1.41
The CAST (Childhood Asperger Syndrome Test): preliminary development of a UK screen for mainstream primary-school-age children. Autism (2002) 1.40