Simon E. Fisher Language and Genetics Department Max Planck Institute for Psycholinguistics Biography Publications Institution JoVE Articles Simon E. Fisher has not added a biography. If you are Simon E. Fisher and would like to personalize this page please email our Author Liaison for assistance. Publications A Genome Wide Association Study of Mathematical Ability Reveals an Association at Chromosome 3q29, a Locus Associated with Autism and Learning Difficulties: a Preliminary Study PloS One. 2014 | Pubmed ID: 24801482 Differences in Cerebral Cortical Anatomy of Left- and Right-handers Frontiers in Psychology. 2014 | Pubmed ID: 24734025 On the Other Hand: Including Left-handers in Cognitive Neuroscience and Neurogenetics Nature Reviews. Neuroscience. Mar, 2014 | Pubmed ID: 24518415 Associations of HLA Alleles with Specific Language Impairment Journal of Neurodevelopmental Disorders. 2014 | Pubmed ID: 24433325 The ENIGMA Consortium: Large-scale Collaborative Analyses of Neuroimaging and Genetic Data Brain Imaging and Behavior. Jan, 2014 | Pubmed ID: 24399358 Increased Prevalence of Sex Chromosome Aneuploidies in Specific Language Impairment and Dyslexia Developmental Medicine and Child Neurology. Apr, 2014 | Pubmed ID: 24117048 Measurement and Genetics of Human Subcortical and Hippocampal Asymmetries in Large Datasets Human Brain Mapping. Nov, 2013 | Pubmed ID: 24827550 Is Synaesthesia More Common in Autism? Molecular Autism. 2013 | Pubmed ID: 24252644 Molecular Genetics of Dyslexia: an Overview Dyslexia (Chichester, England). Nov, 2013 | Pubmed ID: 24133036 Common Variants in Left/right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill PLoS Genetics. 2013 | Pubmed ID: 24068947 Evolution. Culture, Genes, and the Human Revolution Science (New York, N.Y.). May, 2013 | Pubmed ID: 23704558 FOXP2 Targets Show Evidence of Positive Selection in European Populations American Journal of Human Genetics. May, 2013 | Pubmed ID: 23602712 Neurogenomics of Speech and Language Disorders: the Road Ahead Genome Biology. Apr, 2013 | Pubmed ID: 23597266 Absolute Pitch Exhibits Phenotypic and Genetic Overlap with Synesthesia Human Molecular Genetics. May, 2013 | Pubmed ID: 23406871 Persistence and Transmission of Recessive Deafness and Sign Language: New Insights from Village Sign Languages European Journal of Human Genetics : EJHG. Sep, 2013 | Pubmed ID: 23321624 Decoding the Genetics of Speech and Language Current Opinion in Neurobiology. Feb, 2013 | Pubmed ID: 23228431 Dual Copy Number Variants Involving 16p11 and 6q22 in a Case of Childhood Apraxia of Speech and Pervasive Developmental Disorder European Journal of Human Genetics : EJHG. Apr, 2013 | Pubmed ID: 22909776 The DISC1 Promoter: Characterization and Regulation by FOXP2 Human Molecular Genetics. Jul, 2012 | Pubmed ID: 22434823 Foxp2 Mutations Impair Auditory-motor Association Learning PloS One. 2012 | Pubmed ID: 22412993 Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain PLoS Genetics. Jul, 2011 | Pubmed ID: 21765815 Exome Sequencing in Sporadic Autism Spectrum Disorders Identifies Severe De Novo Mutations Nature Genetics. Jun, 2011 | Pubmed ID: 21572417 Molecular Networks Implicated in Speech-related Disorders: FOXP2 Regulates the SRPX2/uPAR Complex Human Molecular Genetics. Dec, 2010 | Pubmed ID: 20858596 언어 장애의 유전학의 최근 발전입니다 Genome Medicine. 2010 | Pubmed ID: 20193051 Genetic Susceptibility to Stuttering The New England Journal of Medicine. Feb, 2010 | Pubmed ID: 20147708 Unravelling Neurogenetic Networks Implicated in Developmental Language Disorders Biochemical Society Transactions. Dec, 2009 | Pubmed ID: 19909259 CMIP 및 ATP2C2 언어 장애에서 음운론 단기 메모리 변조 American Journal of Human Genetics. Aug, 2009 | Pubmed ID: 19646677 Modified Sound-evoked Brainstem Potentials in Foxp2 Mutant Mice Brain Research. Sep, 2009 | Pubmed ID: 19596273 A Humanized Version of Foxp2 Affects Cortico-basal Ganglia Circuits in Mice Cell. May, 2009 | Pubmed ID: 19490899 발달 언어적 Dyspraxia에 FOXP1 돌연변이의 영향을 평가 합니다 European Journal of Human Genetics : EJHG. Oct, 2009 | Pubmed ID: 19352412 FOXP2 As a Molecular Window into Speech and Language Trends in Genetics : TIG. Apr, 2009 | Pubmed ID: 19304338 기능 유전 링크 사이 뚜렷한 발달 언어 장애 The New England Journal of Medicine. Nov, 2008 | Pubmed ID: 18987363 장애 시 냅 스가 소성 및 모터 인간의 음성 적자에 연루 점 돌연변이와 쥐에 있는 학습 Current Biology : CB. Mar, 2008 | Pubmed ID: 18328704 High-throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language Disorders American Journal of Human Genetics. Dec, 2007 | Pubmed ID: 17999362 Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain American Journal of Human Genetics. Dec, 2007 | Pubmed ID: 17999357 Generation of Mice with a Conditional Foxp2 Null Allele Genesis (New York, N.Y. : 2000). Jul, 2007 | Pubmed ID: 17619227 Molecular Windows into Speech and Language Disorders Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP). 2007 | Pubmed ID: 17556856 노래 쥐, 새, 그리고 더 많은: FOXP2 기능과 인간의 음성과 언어 장애에 대 한 모델 The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. Oct, 2006 | Pubmed ID: 17035521 Functional Genetic Analysis of Mutations Implicated in a Human Speech and Language Disorder Human Molecular Genetics. Nov, 2006 | Pubmed ID: 16984964 Tangled Webs: Tracing the Connections Between Genes and Cognition Cognition. Sep, 2006 | Pubmed ID: 16764847 Genes, Cognition and Dyslexia: Learning to Read the Genome Trends in Cognitive Sciences. Jun, 2006 | Pubmed ID: 16675285 The Eloquent Ape: Genes, Brains and the Evolution of Language Nature Reviews. Genetics. Jan, 2006 | Pubmed ID: 16369568 On Genes, Speech, and Language The New England Journal of Medicine. Oct, 2005 | Pubmed ID: 16236736 음성 및 언어 발달 적자의 새로운 원인으로 FOXP2 자르기의 식별 American Journal of Human Genetics. Jun, 2005 | Pubmed ID: 15877281 염색체 6p22.2의 77 Kilobase 지역, 영국에서 및 미국에서 가족 실 독 증에 연결 됩니다 American Journal of Human Genetics. Dec, 2004 | Pubmed ID: 15514892 Attention Deficit Hyperactivity Disorder: Fine Mapping Supports Linkage to 5p13, 6q12, 16p13, and 17p11 American Journal of Human Genetics. Oct, 2004 | Pubmed ID: 15297934 모터 조정과 치러야, 독서 관련 인식에 대 한 가족 및 유전 효과 The American Journal of Psychiatry. Nov, 2003 | Pubmed ID: 14594743 원래 부모 염색체 2 P 12-질문 11에 사용 하는 손 및 정신 분열 증 민감성에 미치는 영향 Human Molecular Genetics. Dec, 2003 | Pubmed ID: 14583442 FOXP2 식 두뇌 개발 하는 동안 심각한 연설 및 언어 장애에서 병리학의 성인 사이트와 일치 한다 Brain : a Journal of Neurology. Nov, 2003 | Pubmed ID: 12876151 FOXP2 in Focus: What Can Genes Tell Us About Speech and Language? Trends in Cognitive Sciences. Jun, 2003 | Pubmed ID: 12804692 확장 된 샘플에 주의-결핍/과잉 행동 장애에 대 한 Genomewide 검색: 17 P 11에 암시 연계 American Journal of Human Genetics. May, 2003 | Pubmed ID: 12687500 2 P 12-질문 11 상대 핸드 스킬의 연계에 대 한 확실 한 증거 American Journal of Human Genetics. Feb, 2003 | Pubmed ID: 12596796 복잡 한 인 지적 특성의 해 부에 대 한 복수 연계 분석의 사용 American Journal of Human Genetics. Mar, 2003 | Pubmed ID: 12587094 음성 및 언어 장애의 유전적 기초를 해독 합니다 Annual Review of Neuroscience. 2003 | Pubmed ID: 12524432 Developmental Dyslexia: Genetic Dissection of a Complex Cognitive Trait Nature Reviews. Neuroscience. Oct, 2002 | Pubmed ID: 12360321 FOXP2, 연설 및 언어에 관련 된 유전자의 분자 진화 Nature. Aug, 2002 | Pubmed ID: 12192408 염색체 자폐증에 연루 지역에서 16 P 13에 주의-결핍/과잉 행동 장애의 유전 결합 American Journal of Human Genetics. Oct, 2002 | Pubmed ID: 12187510 Loci 주의-결핍/과잉 행동 장애에 관련 된 검색을 Genomewide American Journal of Human Genetics. May, 2002 | Pubmed ID: 11923911 염색체 2 P 12-16 실 독 증 민감성 로커 스의 고급 매핑: 양적 협회 분석 및 위치 후보 유전자 SEMA4F 및 OTX1 Psychiatric Genetics. Mar, 2002 | Pubmed ID: 11901358 형제 쌍에서 상대 손 기술에 대 한 Genomewide 연동 화면 American Journal of Human Genetics. Mar, 2002 | Pubmed ID: 11774074 독립적인 게놈 수준의 검사 실 독 증에 영향을 미치는 염색체 18 양적 특성 로커 스를 식별 합니다 Nature Genetics. Jan, 2002 | Pubmed ID: 11743577 생물 발광 공명 에너지 전달을 이용하여 살아있는 세포에서 단백질 - 단백질 상호 작용을 조사 Pelagia Deriziotis*1, Sarah A. Graham*1, Sara B. Estruch1, Simon E. Fisher1,2 1Language and Genetics Department, Max Planck Institute for Psycholinguistics, 2Donders Institute for Brain, Cognition and Behaviour JoVE 51438 Biology
생물 발광 공명 에너지 전달을 이용하여 살아있는 세포에서 단백질 - 단백질 상호 작용을 조사 Pelagia Deriziotis*1, Sarah A. Graham*1, Sara B. Estruch1, Simon E. Fisher1,2 1Language and Genetics Department, Max Planck Institute for Psycholinguistics, 2Donders Institute for Brain, Cognition and Behaviour JoVE 51438 Biology