G. Fisch

发表

Visual Inspection of Data Revisited: Do the Eyes Still Have It?

G. Fisch, G S Fisch, 1998, The Behavior analyst.

Transgenic and knockout models of neuropsychiatric disorders

J. Flint, G. Fisch, 2006 .

HIV Infection Affects Streptococcus mutans Levels, but Not Genotypes

Z. Chen, R. Norman, D. Malamud, 2012, Journal of dental research.

Levels , but Not Genotypes Streptococcus mutans HIV Infection Affects

R. Norman, D. Malamud, G. Fisch, 2012 .

Laterality Preference and Cognition: Cross-Syndrome Comparison of Patients with Trisomy 21 (Down), del7q11.23 (Williams–Beuren) and del22q11.2 (DiGeorge or Velo-Cardio-Facial) Syndromes

V. Volterra, C. Deruelle, N. Philip, 2011, Behavior genetics.

Laterality in persons with intellectual disability II. Hand, foot, ear, and eye laterality in persons with Trisomy 21 and Williams-Beuren syndrome.

V. Volterra, C. Deruelle, G. Fisch, 2006, Developmental Psychobiology.

Mechanisms, models, and mental retardation.

G. Fisch, 2000, American journal of medical genetics.

Models of Human Behavior: Talking to the Animals

G. Fisch, 2009 .

Communication and Language in Animals

G. Fisch, 2015 .

Syndromes and Epistemology I: Autistic spectrum disorders

G. Fisch, 2005, American journal of medical genetics. Part A.

Animal Models and Human Neuropsychiatric Disorders

G. Fisch, 2007, Behavior genetics.

Cognitive‐behavioral features of children with Wolf–Hirschhorn syndrome: Preliminary report of 12 cases

A. Battaglia, B. Parrini, G. Fisch, 2008, American journal of medical genetics. Part C, Seminars in medical genetics.

Cognitive‐behavioral features of Wolf–Hirschhorn syndrome and other subtelomeric microdeletions

A. Battaglia, G. Fisch, R. Simensen, 2010, American journal of medical genetics. Part C, Seminars in medical genetics.

Further evidence for genetic heterogeneity in the fragile X syndrome

W. Brown, G. Fisch, E. Jenkins, 1987, Human Genetics.

Longitudinal changes in cognitive-behavioral levels in three children with FRAXE.

B. Hamel, A. Smits, G. Fisch, 1999, American journal of medical genetics.

Screening developmentally disabled male populations for fragile X: the effect of sample size.

W. Brown, I. Cohen, G. Fisch, 1988, American journal of medical genetics.

Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: growth, development, and profiles.

A. Pandya, G. Fisch, W. Nance, 1999, American journal of medical genetics.

Seventh International Workshop on the Fragile X and X-linked Mental Retardation.

H. Willard, C. Schwartz, W. Brown, 1996, American journal of medical genetics.

2015 William Allan Award Introduction: Kay E. Davies.

G. Fisch, 2016, American journal of human genetics.

Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: a prospective multicenter analysis.

G. Fisch, N. Carpenter, R. Simensen, 1996, American journal of medical genetics.

The Fragile X Syndrome a

W. Brown, I. Cohen, G. Fisch, 1986, Australian family physician.

Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997.

C. Gunter, C. Schwartz, W. Brown, 1999, American journal of medical genetics.

A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype [Letter To Jmg]

S. Warren, A. Taylor, G. Fisch, 2005 .

Genotype–Phenotype Association Studies of Chromosome 8p Inverted Duplication Deletion Syndrome

G. Fisch, R. Davis, J. Youngblom, 2011, Behavior genetics.

Speech-language and the fragile X syndrome: initial findings.

W. Brown, I. Cohen, R. Hagerman, 1987, ASHA.

Streptococcus mutans and Streptococcus sanguinis Colonization Correlated with Caries Experience in Children

Yihong Li, G. Fisch, P. Caufield, 2008, Caries Research.

Associating complex traits with genetic variants: polygenic risk scores, pleiotropy and endophenotypes

G. Fisch, 2021, Genetica.

Deletion 2q37 syndrome: Cognitive‐behavioral trajectories and autistic features related to breakpoint and deletion size

S. South, J. Carey, G. Fisch, 2016, American journal of medical genetics. Part A.

Is fragile X syndrome a pervasive developmental disability? Cognitive ability and adaptive behavior in males with the full mutation.

G. Fisch, N. Carpenter, R. Simensen, 1994, American journal of medical genetics.

Longitudinal changes in IQ among fragile X females: a preliminary multicenter analysis.

J. Fryns, T. Arinami, G. Fisch, 1994, American journal of medical genetics.

Evaluating data from behavioral analysis: visual inspection or statistical models?

Gene S Fisch, G. Fisch, 2001, Behavioural Processes.

Use of a mucoadhesive disk for relief of dry mouth: a randomized, double-masked, controlled crossover study.

G. Fisch, P. Corby, A. Kerr, 2010, Journal of the American Dental Association.

HIV Infection and Microbial Diversity in Saliva

F. Dewhirst, B. Paster, Yihong Li, 2014, Journal of Clinical Microbiology.

Syndromes and epistemology II: Is autism a polygenic disorder?

G. Fisch, 2008, American journal of medical genetics. Part A.

Deep Phenotyping in the -Omic Era: Methodological Issues Facing Neuropsychiatric Disorders

G. Fisch, 2018 .

Fragile X and autism: a multicenter survey.

J. Opitz, W. Brown, D. Fein, 1986, American journal of medical genetics.

The Fragile X Syndrome and the Fragile X Mutation

G. Fisch, M. Hirst, 2003 .

Is autism associated with the fragile X syndrome?

G. Fisch, 1992, American journal of medical genetics.

Safety of direct administration of AAV2(CU)hCLN2, a candidate treatment for the central nervous system manifestations of late infantile neuronal ceroid lipofuscinosis, to the brain of rats and nonhuman primates.

R. Crystal, N. Hackett, G. Fisch, 2005, Human gene therapy.

Longitudinal changes in cognitive and adaptive behavior in fragile X females: a prospective multicenter analysis.

J. Steyaert, J. Fryns, G. Fisch, 1999, American journal of medical genetics.

The fragile X premutation in carriers and its effect on mutation size in offspring.

S. Thibodeau, D. Nelson, G. Fisch, 1995, American journal of human genetics.

Autism and epistemology IV: Does autism need a theory of mind?

G. Fisch, 2013, American journal of medical genetics. Part A.

Clozapine: its impact on aggressive behavior among children and adolescents with schizophrenia.

S. Kumra, G. Fisch, G. Gerbino-Rosen, 2005, Journal of the American Academy of Child and Adolescent Psychiatry.

Longitudinal Assessment of Cognitive- Behavioral Deficits Produced by the Fragile-X Mutation

G. Fisch, 1997 .

Relationship between age and IQ among fragile X males: a multicenter study.

C. Schwartz, J. Fryns, U. Froster-Iskenius, 1991, American journal of medical genetics.

Toothbrush efficacy for plaque removal.

G. Fisch, P. Corby, R. Norman, 2014, International journal of dental hygiene.

A. Pandya, G. Fisch, W. Nance, 1999, American journal of medical genetics.

Developmental trajectories in cognitive‐behavioral phenotypes: Introduction

G. Fisch, 2015, American journal of medical genetics. Part C, Seminars in medical genetics.

Pathogenic significance of deletions distal to the currently described Wolf–Hirschhorn syndrome critical regions on 4p16.3

S. South, J. Vermeesch, G. Fisch, 2008, American journal of medical genetics. Part C, Seminars in medical genetics.

The course of cognitive‐behavioral development in children with the FMR1 mutation, Williams–Beuren syndrome, and neurofibromatosis type 1: The effect of gender

G. Fisch, N. Carpenter, R. Simensen, 2010, American journal of medical genetics. Part A.

Longitudinal Changes in Cognitive and Adaptive Behavior Scores in Children and Adolescents with the Fragile X Mutation or Autism

G. Fisch, R. Simensen, R. Schroer, 2002, Journal of autism and developmental disorders.

Lack of association between mutation size and cognitive/behavior deficits in fragile X males: a brief report.

G. Fisch, N. Carpenter, R. Simensen, 1996, American journal of medical genetics.

Developmental trajectories in syndromes with intellectual disability, with a focus on Wolf-Hirschhorn and its cognitive-behavioral profile.

A. Battaglia, G. Fisch, N. Carpenter, 2012, American journal on intellectual and developmental disabilities.

Cognitive‐behavioral characteristics and developmental trajectories in children with deletion 11qter (Jacobsen syndrome), and their relation to deletion size

G. Fisch, 2015, American journal of medical genetics. Part A.

Longitudinal Changes in Cognitive Ability and Adaptive Behavior in Children and Adolescents with the Fragile X Mutation or Autism.

G. Fisch, R. Simensen, R. Schroer, 2000 .

HIV-induced immunosuppression is associated with colonization of the proximal gut by environmental bacteria

Z. Pei, G. Fisch, C. Nossa, 2015, AIDS.

What is associated with the fragile X syndrome?

G. Fisch, 1993, American journal of medical genetics.

Whither the genotype‐phenotype relationship? An historical and methodological appraisal

G. Fisch, 2017, American journal of medical genetics. Part C, Seminars in medical genetics.

Folic acid treatment of fragile X males: a further study.

W. Brown, I. Cohen, G. Fisch, 1988, American journal of medical genetics.

Neurocognitive Profile in Adolescents with Early-Onset Schizophrenia: Clinical Correlates

Nina Kohn, Robert M. Bilder, Sanjiv Kumra, 2005, Biological Psychiatry.

Studies of age‐correlated features of cognitive‐behavioral development in children and adolescents with genetic disorders

G. Fisch, W. Nance, N. Carpenter, 2007, American journal of medical genetics. Part A.

Laterality in Persons with Intellectual Disability. I—Do Patients with Trisomy 21 and Williams–Beuren Syndrome Differ from Typically Developing Persons?

V. Volterra, C. Deruelle, G. Fisch, 2006, Behavior genetics.

No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome.

B. Oostra, L. Kozák, G. Fisch, 1994, American journal of medical genetics.

Design Aspects of a Case-Control Clinical Investigation of the Effect of HIV on Oral and Gastrointestinal Soluble Innate Factors and Microbes

Yihong Li, R. Norman, D. Malamud, 2014, PloS one.

Cognitive‐behavioral profiles of females with the fragile X mutation

G. Fisch, 2006, American journal of medical genetics. Part A.

FMR1 gene and fragile X syndrome.

J. Mandel, B. Bardoni, G. Fisch, 2000, American journal of medical genetics.

Autism and the fragile X syndrome.

W. Brown, I. Cohen, G. Fisch, 1986, The American journal of psychiatry.

A study of the use of nonverbal systems in the differential diagnosis of autistic, mentally retarded and fragile X individuals

I. Cohen, G. Fisch, E. Wolf-Schein, 1985 .

9th international workshop on fragile X syndrome and X-linked mental retardation.

G. Ramakers, D. Nelson, C. Schwartz, 2000, American journal of medical genetics.

Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?

C. Schwartz, J. Fryns, T. Arinami, 1992, American journal of medical genetics.

Learning and memory in the FMR1 knockout mouse.

B. Oostra, G. Fisch, C. Bakker, 1999, American journal of medical genetics.

Social gaze, social avoidance, and repetitive behavior in fragile X males: a controlled study.

W. Brown, I. Cohen, R. Hagerman, 1988, American journal of mental retardation : AJMR.

Autism and epistemology III: Child development, behavioral stability, and reliability of measurement

G. Fisch, 2012, American journal of medical genetics. Part A.

Nosology and epidemiology in autism: Classification counts

Gene S Fisch, G. Fisch, 2012, American journal of medical genetics. Part C, Seminars in medical genetics.

The Genetics and Genomics of Neurobehavioral Disorders

G. Fisch, 2003 .

Fragile X syndrome in females with autism.

W. Brown, I. Cohen, G. Fisch, 1989, American journal of medical genetics.

Nonsyndromal Mental Retardation Associated with the FRAXE Fragile Site and the FMR2 Gene

J. Gécz, G. Fisch, 2003 .

Fragile X and autism.

G. Fisch, 1989, Journal of the American Academy of Child and Adolescent Psychiatry.

Genetic and other factors that contribute to variability in cytogenetic expression in fragile X males.

W. Silverman, G. Fisch, E. Jenkins, 1991, American journal of medical genetics.

Reliability of diagnostic assessment of normal and premutation status in the fragile X syndrome using DNA testing.

S. Thibodeau, D. Nelson, G. Fisch, 1994, American journal of medical genetics.

Factors which contribute to cytogenetic frequency of expression in families of fragile X females.

J. Fryns, G. Fisch, 1992, American journal of medical genetics.

High dose folic acid treatment of fragile (X) males.

W. Brown, I. Cohen, G. Fisch, 1986, American journal of medical genetics.

eurocognitive Profile in Adolescents with Early-Onset chizophrenia : Clinical Correlates

S. Kumra, K. Cervellione, K. Burdick, 2005 .

Psychological assessment in XLMR: a proposal for setting international standards.

G. Fisch, 2000, Genetic counseling.

Developmental trajectories in cognitive‐behavioral phenotypes: Introduction

G. Fisch, 2015, American Journal of Medical Genetics. Part C, Seminars in Medical Genetics.

Psychology genetics.

G. Fisch, 2000, American journal of medical genetics.

Mental retardation or intellectual disability? Time for a change

G. Fisch, 2011, American journal of medical genetics. Part A.