M. Spence

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M. Spence, S. Hodge, 1986 .

Loss of information due to ambiguous haplotyping of SNPs

M. Boehnke, M. Spence, S. Hodge, 1999, Nature Genetics.

Extensions to pedigree analysis III. Variance components by the scoring method

K. Lange, M. Spence, J. Westlake, 1976, Annals of human genetics.

A replication of the Autism Diagnostic Observation Schedule (ADOS) revised algorithms.

Geraldine Dawson, Andrew Pickles, Sally Rogers, 2008, Journal of the American Academy of Child and Adolescent Psychiatry.

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.

P. Visscher, S. Cichon, N. Freimer, 2003, American journal of human genetics.

Evidence of positive selection acting at the human dopamine receptor D4 gene locus

J. Swanson, K. Kidd, M. Spence, 2001, Proceedings of the National Academy of Sciences of the United States of America.

High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder

J. Swanson, M. Spence, R. Moyzis, 2003, Molecular Psychiatry.

The genetic architecture of selection at the human dopamine receptor D4 (DRD4) gene locus.

J. Swanson, K. Kidd, M. Spence, 2004, American journal of human genetics.

Head circumference and height in autism: A study by the collaborative program of excellence in autism

Geraldine Dawson, Michelle Dunn, Sally Rogers, 2006, American journal of medical genetics. Part A.

Attention deficit/hyperactivity disorder children with a 7-repeat allele of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychological tests of attention.

M I Posner, M A Spence, M. Posner, 2000, Proceedings of the National Academy of Sciences of the United States of America.

A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22.

M A Spence, J L Brown, S Ungerleider, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Dopamine genes and ADHD

Michael Murias, Sabrina Schuck, Pamela Flodman, 2000, Neuroscience & Biobehavioral Reviews.

Resolving genetic models for the transmission of schizophrenia

M. Spence, D. Rao, I. Gottesman, 1985, Genetic epidemiology.

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene

J. Piven, V. Sheffield, T. Wassink, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq.

P. M. Falk, P. Green, M. Spence, 1990, American journal of human genetics.

Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract.

M. Spence, J. Bateman, R. Berry, 2006, American journal of ophthalmology.

Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA)

M. Spence, J. Bateman, P. Flodman, 2008, American journal of medical genetics. Part A.

The “Circular” Problems of Calculating Risk: Dealing with Consanguinity

M. Spence, S. Hodge, 2000, Journal of Genetic Counseling.

Genetic linkage studies with neurofibromatosis: the question of heterogeneity.

M. Spence, S. Bale, V. Cortessis, 1987, Journal of medical genetics.

One or two genetic loci mediate high opiate analgesia in selectively bred mice

M. Spence, J. Mogil, P. Flodman, 1995, Pain.

Possible heterogeneity in the segregation pattern of breast cancer in families with bilateral breast cancer

M. Spence, D. Rao, A. Paganini-Hill, 1988, Genetic epidemiology.

Relation of metabolic syndrome components to left ventricular mass in Mexican Americans versus non-Hispanic whites.

M. Spence, J. Gardin, N. Wong, 2010, Metabolism: clinical and experimental.

Cowden disease: gene marker studies and measurements of epidermal growth factor.

M. Spence, D. Orth, R. Sparkes, 1986, American journal of human genetics.

Do differences in subclinical cardiovascular disease in mexican americans versus European americans help explain the Hispanic paradox?

M. Spence, J. Gardin, R. Detrano, 2010, The American journal of cardiology.

A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.

J. Sikela, M. Spence, J. Bateman, 2000, Investigative ophthalmology & visual science.

Application of the lod method to the detection of linkage between a quantitative trait and a qualitative marker: a simulation experiment.

M. Spence, M. B. Frank, K. Lange, 1976, American journal of human genetics.

A genetic epidemiologic investigation of breast cancer in families with bilateral breast cancer. II. Linkage analysis

M. Spence, A. Paganini-Hill, R. Haile, 1989, Clinical genetics.

HLA and the inheritance of multiple sclerosis: linkage analysis of 72 pedigrees.

M. Spence, S. Hodge, P. Terasaki, 1980, American journal of human genetics.

Possible heterogeneity in the phosphoglycolate phosphatase (PGP)-haptoglobin alpha (HPA) linkage.

M. Spence, A. Chakravarti, S. Bale, 1984, American journal of human genetics.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Thomas Bourgeron, Alberto Segre, Alberto Maria Segre, 2007, Nature Genetics.

Evidence for genetic linkage of autism to chromosomes 7 and 4

G. Dawson, A. Estes, N. Minshew, 2006, Molecular Psychiatry.

Statement on use of DNA testing for presymptomatic identification of cancer risk. National Advisory Council for Human Genome Research.

Lloyd M. Smith, J. R. Cox, D. Botstein, 1994, JAMA.

Proopiomelanocortin (POMC) disregulation and response to opiate blockers

M. Spence, C. Sandman, Moyra J. Smith, 1999 .

Some effects of selection strategies on linkage analysis

K. Kidd, M. Spence, S. Hodge, 1988, Genetic epidemiology.

International Genetic Epidemiology Society: Commentary on Darkness in El Dorado by Patrick Tierney

M. Baur, M. Spence, N. Morton, 2001, Genetic epidemiology.

A Genetic Study of Schizophrenia Pedigrees

R. Elston, M. Spence, K. Namboodiri, 1976 .

A genetic study of schizophrenia pedigrees. II. One-locus hypotheses.

R. Elston, M. Spence, K. Namboodiri, 1978, Neuropsychobiology.

Mental retardation associated with "balanced" chromosome rearrangements.

M. Spence, R. Sparkes, S. Funderburk, 1977, American journal of human genetics.

Estimation of polygenic recurrence risk for cleft lip and palate.

M. Spence, J. Westlake, K. Lange, 1976, Human heredity.

Cleft lip with or without cleft palate in Shanghai, China: evidence for an autosomal major locus.

M. Spence, D. Hu, M. Marazita, 1992, American journal of human genetics.

Genetic linkage studies of transferrin, pseudocholinesterase, and chromosome 1 loci.

M. Spence, P. Garry, L. Field, 1984, Human Heredity.

Stoppage: An issue for segregation analysis

M. Spence, S. Hodge, T. Foroud, 2001, Genetic epidemiology.

High prevalence of rare receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder.

M. Spence, P. Flodman, H. Chi, 2003 .

Genetic linkage analysis of the carpal tunnel syndrome.

M. Spence, M. Marazita, R. Gray, 1985, Human heredity.

Bipolar disorder: Dominant or recessive on chromosome 5?

M. Spence, P. Flodman, J. Homer, 1997, Genetic epidemiology.

Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa.

M. Spence, J. Bateman, J. Heckenlively, 1996, American journal of human genetics.

Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locus.

R. Cantor, M. Spence, D. Curtis, 1993, Transactions of the American Ophthalmological Society.

Some epistatic two-locus models of disease. II. The confounding of linkage and association.

M. Spence, S. Hodge, 1981, American journal of human genetics.

Endothelial function and urine albumin levels among asymptomatic Mexican-Americans and non-Hispanic whites

M. Spence, J. Gardin, N. Wong, 2008, Cardiovascular ultrasound.

Interaction of HLA and immunoglobulin antigens in Type 1 (insulin-dependent) diabetes

M. Spence, S. Hodge, J. Rotter, 1984, Diabetologia.

A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.

M. Spence, J. Bateman, P. Flodman, 2006, Investigative ophthalmology & visual science.

Response to Craddock et al.

M. Spence, R. Remick, J. Bailey-Wilson, 1997 .

Estimating Recombination Fraction Separately for Males and Females: A Counterintuitive Result

M. Spence, S. Hodge, P. Flodman, 1998, Human Heredity.

Genetic heterogeneity of hyperpepsinogenemic I and normopepsinogenemic I duodenal ulcer disease.

M. Spence, J. Rotter, G. Petersen, 1979, Annals of internal medicine.

Cleft lip with or without cleft palate: Reanalysis of a three‐generation family study from England

M. Spence, A. Goldstein, D. Rao, 1986, Genetic epidemiology.

Major gene determination of liability to cleft lip with or without cleft palate: a multiracial view.

M. Spence, M. Marazita, M. Melnick, 1986, Journal of craniofacial genetics and developmental biology. Supplement.

Genotypic and phenotypic analysis of 396 individuals with mutations in Sonic Hedgehog

M. Spence, S. Bale, A. Paulussen, 2012, Journal of Medical Genetics.

The Genetics of Hypodontia

M. Spence, B. K. Suarez, 1974, Journal of dental research.

The S-leut anthropometric traits: genetic analysis.

M. Spence, A. Paganini-Hill, A. Martin, 1981, American journal of physical anthropology.

Simulated data for a complex genetic trait (Problem 2 for GAW11): How the model was developed, and why

M. Spence, S. Hodge, C. Falk, 1999, Genetic epidemiology.

Mortality, hepatopathy and liver copper concentrations in artificially reared Jersey calves before and after reductions in copper supplementation

M. Spence, A. Macrae, H. Martineau, 2012, Veterinary Record.

Ataxia-telangiectasia and xeroderma pigmentosum: no evidence of linkage to HLA.

M. Spence, S. Hodge, R. Gatti, 2008, Tissue antigens.

Gaucher disease. Current issues in diagnosis and treatment. NIH Technology Assessment Panel on Gaucher Disease.

W. H. Hall, Robin E Berman, F. Collins, 1996, JAMA.

Oral Physostigmine and Inherited Ataxias

M. Spence, J. Blass, R. Kark, 1979 .

Physostigmine in familial ataxias

M. Spence, J. Blass, R. A. Pieter Kark, 1977, Neurology.

A new locus for autosomal dominant cataract on chromosome 12q13.

M. Spence, J. Bateman, R. Berry, 2000, Investigative ophthalmology & visual science.

Evidence for multiple loci from a genome scan of autism kindreds

G. Dawson, A. Estes, N. Minshew, 2006, Molecular Psychiatry.

Presence of large deletions in kindreds with autism.

Ellen M Wijsman, Geraldine Dawson, Pamela Flodman, 2002, American journal of human genetics.

CLOSE GENETIC LINKAGE BETWEEN DIABETES MELLITUS AND KIDD BLOOD GROUP

M. Spence, S. Hodge, J. Rotter, 1981, The Lancet.

Bipolar disorder: evidence for a major locus.

M. Spence, A. Sadovnick, R. Remick, 1995, American journal of medical genetics.

Possible locus for bipolar disorder near the dopamine transporter on chromosome 5.

J. Kelsoe, M. Spence, A. Sadovnick, 1996, American journal of medical genetics.

Sequence variants of the DRD4 gene in autism: Further evidence that rare DRD4 7R haplotypes are ADHD specific

J. Swanson, M. Spence, P. Flodman, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Autism and genetics. A decade of research.

M. Spence, R. Asarnow, S. Smalley, 1988, Archives of general psychiatry.

Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism.

M. Spence, B. Freeman, M. Marazita, 1985, The American journal of psychiatry.

Ultrasonographic detection of orbicularis oris defects in first degree relatives of isolated cleft lip patients.

M A Spence, M. Spence, W. Neufeld-Kaiser, 2000, American journal of medical genetics.

A genetic linkage map of the rat derived from recombinant inbred strains

M. Spence, G. Lathrop, D. Gauguier, 1996, Mammalian Genome.

Mitochondrial and ion channel gene alterations in autism.

M. Spence, R. Naviaux, D. Wallace, 2012, Biochimica et biophysica acta.

Heart Rate and Blood Pressure Quantitative Trait Loci for the Airpuff Startle Reaction

M. Spence, V. Křen, M. Pravenec, 2002, Hypertension.

Recombinational event between Norrie disease and DXS7 loci

M. Spence, V. Cortessis, R. Sparkes, 1988, Clinical genetics.

Genetic linkage analysis of autosomal dominant congenital cataracts.

M. Spence, J. Bateman, M. Marazita, 1986, American journal of ophthalmology.

Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor gene

M. Pericak-Vance, M. Spence, R. Martuza, 1987, Cell.

Nuclear and Mitochondrial Genome Defects in Autisms

M. Spence, Moyra J. Smith, P. Flodman, 2009, Annals of the New York Academy of Sciences.

Association studies between type 1 (insulin-dependent) diabetes and 27 genetic markers: Lack of association between type 1 diabetes and kidd blood group

M. Spence, S. Hodge, J. Rotter, 1983, Diabetologia.

Human gene mapping, genetic linkage, and clinical applications.

T. Mohandas, L. Shapiro, M. Spence, 1980, Annals of internal medicine.

Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene

M. Spence, G. Pescia, F. Munier, 1992, Human Genetics.

Early Regression in Social Communication in Autism Spectrum Disorders: A CPEA Study

G. Dawson, C. Lord, W. McMahon, 2005, Developmental neuropsychology.

Genetic linkage analysis in a high-risk cancer family: HLA and 24 other markers.

M. Spence, L. Field, M. Freidin, 1983, Cancer genetics and cytogenetics.

Genetic linkage study of bipolar disorder and the serotonin transporter.

J. Kelsoe, M. Spence, R. Blakely, 1996, American journal of medical genetics.

COMPUTATIONS FOR PRENATAL PREDICTION OF MYOTONIC DYSTROPHY

M. Spence, K. Lange, B. Crandall, 1976, The Lancet.

Development and validation of a measure of dysmorphology: Useful for autism subgroup classification

M. Spence, N. Flournoy, J. Miles, 2008, American journal of medical genetics. Part A.

Autism and the serotonin transporter: the long and short of it

G. Dawson, N. Minshew, E. Cook, 2005, Molecular Psychiatry.

Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network

G. Dawson, W. McMahon, N. Minshew, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.

G. Dawson, W. McMahon, E. Cook, 2002, American journal of medical genetics.

Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR

M. Spence, P. Filipek, Moyra J. Smith, 2001, Cytogenetic and Genome Research.

Linkage analysis of neurofibromatosis (von Recklinghausen disease).

M. Spence, L. Field, A. Rubenstein, 1983, Journal of medical genetics.

Recklinghausen disease ) . neurofibromatosis ( von Linkage analysis of

M. Spence, L. Field, A. Rubenstein, 2022 .

Genetic analyses of pyloric stenosis suggesting a specific maternal effect.

K. Kidd, M. Spence, 1976, Journal of medical genetics.

Genetics of essential hypertension.

M. Spence, T. Kurtz, Theodore W. Kurtz, 1993, The American journal of medicine.

Language and Other Regression: Assessment and Timing

Pamela Flodman, M. Spence, P. Filipek, 2003, Journal of autism and developmental disorders.

Oligogenic determination of morphine analgesic magnitude: A genetic analysis of selectively bred mouse lines

M. Spence, J. Belknap, J. Mogil, 1995, Behavior genetics.

Mitochondrial dysfunction in autistic patients with 15q inverted duplication

Jenifer Juranek, M. Spence, P. Filipek, 2003, Annals of neurology.

A radiation hybrid map of human chromosome 5 with integration of cytogenetic, genetic, and transcript maps.

D. Church, J. McPherson, M. Lovett, 1997, Genome research.

Genetic control of the eighth component of complement.

B. H. Petersen, M. Spence, N. Day, 1979, The Journal of clinical investigation.

The emperor's new methods.

Susan E Hodge, Veronica J Vieland, V. Vieland, 2003, American journal of human genetics.

Familial Autoimmune Thyroid Disease as a Risk Factor for Regression in Children with Autism Spectrum Disorder: A CPEA Study

G. Dawson, C. Lord, W. McMahon, 2006, Journal of autism and developmental disorders.

Evidence for a possible major gene effect in absolute finger ridge count.

R. Elston, M. Spence, W. Pollitzer, 1973, Human heredity.

Hereditary multiple exostoses. Report of a family.

M. Spence, L. Field, B. Crandall, 1984, Clinical orthopaedics and related research.

Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13.

M. Spence, P. Filipek, M. Smith, 2000, American journal of medical genetics.

Rightward hemispheric asymmetries in auditory language cortex in children with autistic disorder: an MRI investigation

N. Gage, M. Spence, P. Filipek, 2009, Journal of Neurodevelopmental Disorders.

Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): evidence of an RP locus on chromosome 1.

M. Spence, J. Heckenlively, R. Sparkes, 1977, American journal of human genetics.

Power, mode of inheritance, and type I error in LOD scores and affecteds-only methods: reply to Kruglyak.

S E Hodge, M A Spence, V J Vieland, 1998, American journal of human genetics.

Methodological issues in linkage analyses for psychiatric disorders: secular trends, assortative mating, bilineal pedigrees. Report of the MacArthur Foundation Network I Task Force on Methodological Issues.

R C Elston, S E Hodge, M A Spence, 1993, Human heredity.

Linkage studies of bipolar disorder: methodologic and analytic issues. Report of MacArthur Foundation Workshop on Linkage and Clinical Features in Affective Disorders.

D. Kupfer, M. Spence, K. Merikangas, 1989, Archives of general psychiatry.

Affecteds-only linkage methods are not a panacea.

S E Hodge, M A Spence, V J Vieland, 1996, American journal of human genetics.

Performance comparison of two-point linkage methods using microsatellite markers flanking known disease locations

V. Vieland, M. Spence, M. Logue, 2005, BMC Genetics.

Genes and attention-deficit hyperactivity disorder

M. Posner, C. Deutsch, J. Swanson, 2001, Clinical Neuroscience Research.

A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R

M. Spence, A. Woodroffe, Moyra J. Smith, 2004, BMC Medical Genetics.

Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataract.

M. Spence, J. Bateman, P. Flodman, 2007, Ophthalmology.

Hypoxanthine-guanine phosphoribosyltransferase and deutan colour blindness: the relative positions of their loci on the X-chromosome.

M. Spence, B. Emmerson, D. Wallace, 1973, Advances in experimental medicine and biology.

Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.

M. Spence, D. Janz, R. Sparkes, 1991, American journal of medical genetics.

Genetic Control ofthe Eighth Component ofComplement

B. H. Petersen, M. Spence, C. Alper, 1979 .

Linkage relations of the phenylthiocarbamide locus (PTC).

M. Spence, B. Crandall, 1974, Human heredity.

Pedigree analysis to determine the mode of inheritance in a family with retinitis pigmentosa

R. Elston, M. Spence, S. D. CedeKbaum, 1974, Clinical genetics.

Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosa.

M. Spence, J. Heckenlively, L. Field, 1982, Journal of medical genetics.

Possible assignment of a dominant retinitis pigmentosa gene to chromosome 1.

M. Spence, J. Heckenlively, L. Field, 1982, Ophthalmic research.

Ornithine aminotransferase (OAT): recombination between an X-linked OAT sequence (7.5 kb) and the Norrie disease locus.

T. Mohandas, M. Spence, J. Kivlin, 1990, Genomics.

Norrie disease: linkage analysis using a 4.2-kb RFLP detected by a human ornithine aminotransferase cDNA probe.

T. Mohandas, M. Spence, J. Bateman, 1989, Genomics.

Evaluation of metaphase association patterns for acrocentric chromosomes in the order Cetacea.

M. Spence, D. Duffield, C. Paquin, 1978, Cytologia.

Does theory of mind performance differ in children with early-onset and regressive autism?

M. Spence, A. Lukowski, K. Osann, 2012, Developmental science.

Performance on Cambridge Neuropsychological Test Automated Battery Subtests Sensitive to Frontal Lobe Function in People with Autistic Disorder: Evidence from the Collaborative Programs of Excellence in Autism Network

G. Dawson, W. McMahon, N. Minshew, 2004, Journal of autism and developmental disorders.

Cleft lip with or without cleft palate and dermatoglyphic asymmetry: evaluation of a Chinese population.

M. Spence, D. Hu, S. Weinberg, 2002, Orthodontics & craniofacial research.

The effect of rate stress on the auditory brainstem response in autism: A preliminary report

N. Gage, M. Spence, A. Isenberg, 2010, International journal of audiology.

Genetic linkage analysis of autosomal dominant congenital cataracts with lens-specific DNA probes and polymorphic phenotypic markers.

D. J. Barrett, M. Spence, J. Bateman, 1988, Ophthalmology.

Putative non-Mendelian transmission of retinoblastoma in males: a phenotypic segregation analysis of 150 pedigrees

M. Spence, P. Flodman, F. Munier, 1994, Human Genetics.

Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigrees.

M. Spence, L. Donoso, F. Munier, 1993, Archives of ophthalmology.

A goodness-of-fit test for the polygenic threshold model: application to pyloric stenosis.

K. Lange, M. Spence, K. Gladstien, 1978, American journal of medical genetics.

Absence of measurable linkage between the loci for hypoxanthine-guanine phosphoribosyltransferase and deutan colorblindness.

M. Spence, B. Emmerson, D. Wallace, 1974, American journal of human genetics.

Association Between Amygdala Volume and Anxiety Level: Magnetic Resonance Imaging (MRI) Study in Autistic Children

Jenifer Juranek, Kathryn Osann, Gholam R Berenji, 2006, Journal of child neurology.

Evidence for heritability of biogenic amine levels in the cerebrospinal fluid of rhesus monkeys

D. Kupfer, M. Spence, G. Kraemer, 1995, Biological Psychiatry.

Title No evidence for linkage of liability to autism to HOXA 1 in a sample from the CPEA network Permalink

G. Dawson, W. McMahon, E. Cook, 2002 .

Huntington disease: linkage analysis with age-of-onset corrections.

M. Spence, S. Hodge, B. Crandall, 1980, American journal of medical genetics.

Severe combined immunodeficiency among the Navajo. I. Characterization of phenotypes, epidemiology, and population genetics.

M. Spence, C. Ritenbaugh, A. Hayward, 1991, Human biology.

Is There a ‘Regressive Phenotype’ of Autism Spectrum Disorder Associated with the Measles-Mumps-Rubella Vaccine? A CPEA Study

G. Dawson, C. Lord, W. McMahon, 2006, Journal of autism and developmental disorders.

Use of Home Videotapes to Confirm Parental Reports of Regression in Autism

M. Spence, K. Osann, W. Goldberg, 2008, Journal of autism and developmental disorders.

Genetic linkage studies in Alzheimer's disease

M A Spence, M. Spence, A. Heyman, 1986, Neurology.

State of the science in autism: Report to the National institutes of health

H. Kraemer, C. Lord, N. Minshew, 1996, Journal of autism and developmental disorders.

Genetic susceptibility to multiple sclerosis: a linkage analysis with age‐of‐onset corrections

M. Spence, S. Hodge, R. Detels, 1980, Clinical genetics.

No evidence for linkage between an insulin‐dependent diabetes mellitus‐susceptibility locus and immunoglobulin loci KM or GM

M. Spence, A. Goldstein, D. Rao, 1984, Genetic epidemiology.

Genetic Linkage Analysis of Neurofibromatosis a

M. Spence, M. Marazita, J. Mulvihill, 1986, Annals of the New York Academy of Sciences.

Genetic Linkage Analysis of Neurofibromatosis with DNA Markers a

M. Spence, T. Gilliam, J. Gusella, 1986, Annals of the New York Academy of Sciences.

Diabetes: Evidence from Pairs of Affected Siblings

M. Spence, L. Field, C. Anderson, 2006 .

Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention‐deficit/hyperactivity disorder (ADHD): Increased prevalence of the 2‐repeat allele

J. Swanson, M. Spence, R. Moyzis, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Brief Report: Early Social Communication Behaviors in the Younger Siblings of Children with Autism

M. Spence, P. Filipek, K. Osann, 2005, Journal of autism and developmental disorders.

HLA Sharing and History of Miscarriage among Women with Rheumatoid Arthritis

M. Spence, D. Greenberg, Verónica, 2006 .

Molecular genetic delineation of a deletion of chromosome 13q12→q13 in a patient with autism and auditory processing deficits

M. Spence, A. Woodroffe, P. Filipek, 2003, Cytogenetic and Genome Research.

Genetic Analysis Workshop 13: Analysis of Longitudinal Family Data for Complex Diseases and Related Risk Factors

Joan E Bailey-Wilson, Christopher I Amos, Rita M Cantor, 2003, BMC Genetics.

Genetic influences on spatial ability: Transmission in an extended kindred

M. Spence, S. Smalley, A. Thompson, 1989, Behavior genetics.

A goodness-of-fit test for the polygenic threshold model: application to multiple sclerosis.

M. Spence, A. Sadovnick, S. Tideman, 1981, American journal of medical genetics.