M. E. Hodes

发表

Subtle changes among presymptomatic carriers of the Huntington's disease gene

E. Siemers, T. Foroud, J. Christian, 2000, Journal of neurology, neurosurgery, and psychiatry.

Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset.

Karen Marder, Norman Arnheim, Ira Shoulson, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Gerstmann‐Sträussler‐Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients

D. Dickson, B. Ghetti, S. Perlman, 1995, Neurology.

Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales.

E. Siemers, T. Foroud, J. Christian, 2002, Journal of psychiatric research.

Diverse cell death pathways result from a single missense mutation in weaver mouse.

B. Ghetti, S. Bayer, R. Piva, 1997, The American journal of pathology.

Study of two cases of ring 13 chromosome using high-resolution banding.

I. M. Jones, D. Weaver, M. E. Hodes, 1981, American journal of human genetics.

Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15.

C. Jackson, M. E. Hodes, P. Conneally, 1993, Connective tissue research.

Pachyonychia congenita and steatocystoma multiplex

A. Norins, M. E. Hodes, 1977, Clinical genetics.

The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromes

T. Reed, M. E. Hodes, C. Palmer, 2004, Human Genetics.

Hypothalamic-Pituitary-Gonadal Axis in the Mutant Weaver Mouse

B. Ghetti, A. Heller, M. E. Hodes, 1998, Neuroendocrinology.

Genetic family history questionnaire

M. E. Hodes, A. D. Merritt, P. M. Conneally, 1978, Journal of medical genetics.

Chromosome 6: linkage of the eighth component of complement (C8) to the histocompatibility region (HLA).

B. H. Petersen, D. Meyers, M. E. Hodes, 1976, Birth defects original article series.

Branchio‐oto‐renal dysplasia and branchio‐oto dysplasia: Two distinct autosomal dominant disorders

W. Nance, M. E. Hodes, H. Yune, 1978, Clinical genetics.

Four new cases of ring 21 and 22 including familial transmission of ring 21.

T. Reed, M. E. Hodes, C. Palmer, 1977, Journal of medical genetics.

Brief clinical report: prune belly syndrome in an anencephalic male.

M. Butler, M. E. Hodes, E. Keitges, 1983, American journal of medical genetics.

Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15.

J. Beckmann, T. Foroud, J. Tischfield, 1992, Genomics.

Clinical experience with trisomies 18 and 13.

T. Reed, M. E. Hodes, C. Palmer, 1978, Journal of medical genetics.

Urorectal septum malformation sequence. Report of six cases and embryological analysis.

D. Weaver, M. E. Hodes, M. Mitchell, 1987, American journal of diseases of children.

Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter

J. Haines, J. Christian, M. E. Hodes, 1987, Human Genetics.

Transmission of a balanced homologous t(22q;22q) translocation from mother to normal daughter

S. Schwartz, M. E. Hodes, C. Palmer, 1980, Clinical genetics.

Juvenile chronic granulocytic leukemia in a patient with trisomy 8, neurofibromatosis, and prolonged Epstein-Barr virus infection.

N. Heerema, D. Weaver, M. E. Hodes, 1983, The Journal of pediatrics.

Trisomy 7 mosaicism and manifestations of Goldenhar syndrome with unilateral radial hypoplasia.

D. Weaver, D. Girod, M. E. Hodes, 1981, Journal of craniofacial genetics and developmental biology.

Cartilage-hair hypoplasia, defective T-cell function, and Diamond-Blackfan anemia in an Amish child.

D. Weaver, M. E. Hodes, R. Harris, 1981, American journal of medical genetics.

Neural tube defects in dup(11 q)

M. E. Hodes, P. Bader, R. Munsick, 1984 .

Brief clinical report: a child with radius aplasia, cleft of lip and palate, microcephaly, and unusual chromosome findings.

M. Bull, M. Butler, M. E. Hodes, 1982, American journal of medical genetics.

Cellular distribution of the RNA transcripts of a newly discovered gene in the brain of normal, weaver, Purkinje cell degeneration and reeler mutant mice as evidenced by in situ hybridization histochemistry.

B. Ghetti, M. E. Hodes, L. Sangameswaran, 1993, Brain research. Molecular brain research.

Craniofacial pattern profile (CFPP) evaluation of facial dysmorphology in a familial syndrome with corneal anesthesia and multiple congenital anomalies.

M. E. Hodes, M. Ramos-Arroyo, S. S. Saksena, 1987, American journal of physical anthropology.

Congenital corneal anesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and mental retardation: a new syndrome?

M. E. Hodes, M. Ramos-Arroyo, M. Modes, 1987, American journal of medical genetics.

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

S. Prusiner, B. Ghetti, T. Foroud, 1992, Nature Genetics.

Longitudinal personality changes among presymptomatic Huntington disease gene carriers.

E. Siemers, T. Foroud, J. Christian, 2002, Neuropsychiatry, neuropsychology, and behavioral neurology.

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

S. Prusiner, B. Ghetti, M. Farlow, 1992, Nature Genetics.

Linkage analysis in a large kindred with autosomal dominant transmission of polyglandular autoimmune disease type II (Schmidt syndrome).

M. Butler, M. E. Hodes, P. Conneally, 1984, American journal of medical genetics.

Characterization of murine Girk2 transcript isoforms: structure and differential expression.

R. Piva, M. E. Hodes, S. Dlouhy, 1998, Genomics.

Brief clinical report: two children with de novo del(9p).

S. Kaler, M. E. Hodes, P. Bader, 1983, American journal of medical genetics.

Brief cytogenetic case report: A 4.5‐year‐old girl with deletion 4q syndrome — de novo, 46,XX, del(4) (pter→q31:)

J. Opitz, D. Weaver, M. E. Hodes, 1982 .

Clinical experience withtrisomies 18and131

T. Reed, M. E. Hodes, C. Palmer, 1978 .

Linkage mapping of microdissected clones from distal mouse chromosome 16

B. Ghetti, M. E. Hodes, S. Dlouhy, 1996, Somatic cell and molecular genetics.

Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers.

E. Siemers, J. Stout, T. Foroud, 1999, Archives of neurology.

Direct cDNA selection with DNA microdissected from mouse chromosome 16: isolation of novel clones and construction of a partial transcription map of the C3-C4 region.

B. Ghetti, M. E. Hodes, S. Dlouhy, 1996, Genome research.

Gonadotropin-Releasing Hormone and Regulation of the Gonadal Axis

B. Ghetti, A. Heller, M. E. Hodes, 1998 .

Cognitive scores in carriers of huntington's disease gene compared to noncarriers

E. Siemers, T. Foroud, J. Christian, 1995, Annals of neurology.

Properties and tissue distribution of mouse monomeric carbonyl reductase.

Y. Yamamoto, A. Hara, S. Ishikura, 1998, Biological & pharmaceutical bulletin.

Fournew casesofring 21and22including familial transmission ofring 21

T. Reed, M. E. Hodes, C. Palmer, 1977 .

Phenotypic effects of the weaver gene are evident in the embryonic cerebellum but not in the ventral midbrain.

B. Ghetti, S. Bayer, M. E. Hodes, 1996, Brain research. Developmental brain research.

X‐linked recessive inheritance of ataxia and adult‐onset dementia

M. Farlow, M. E. Hodes, W. Demyer, 1987, Neurology.

DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNA.

L. Madisen, M. Hodes, M. E. Hodes, 1987, American journal of medical genetics.

Motor changes in presymptomatic Huntington disease gene carriers.

J C Christian, J A Norton, P M Conneally, 1996, Archives of neurology.

New syndrome: renal dysplasia, mesomelia, and radiohumeral fusion.

T. Ulbright, M. E. Hodes, C. Ulbright, 1984, American journal of medical genetics.

Anamalous electrophoresis behavior of rebonuclease from human urine and a novel treatment method for reliable analysis

M. Hodes, M. E. Hodes, JOHN MEYRICK Thomas, 1981 .

Novel cDNA clones obtained by antibody screening of a mouse cerebellar cDNA expression library.

B. Ghetti, Fan Luo, M. E. Hodes, 1994, Brain research. Molecular brain research.

Two children with de novo del(9p)

J. Opitz, S. Kaler, M. E. Hodes, 1983 .

Treatment of neoplastic diseases with an improved oral preparation of vinblastine sulfate

W. H. Bond, M. Hodes, M. E. Hodes, 1966, Cancer.

Peripheral Neuropathy Caused by Proteolipid Protein Gene Mutations

G. Kraft, R. Lewis, T. Bird, 1999, Annals of the New York Academy of Sciences.

Heterogeneous duplications in patients with Pelizaeus-Merzbacher disease suggest a mechanism of coupled homologous and nonhomologous recombination.

N. Carter, H. Heng, M. Ross, 2005, American journal of human genetics.

Possible localization of a major gene for cleft lip and palate to 4q

T. Foroud, M. E. Hodes, P. Conneally, 1994, Clinical genetics.

The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2

B. Ghetti, Shengwen Zhang, Lei Yu, 1996, FEBS letters.

Nonsense mutation in exon 3 of the proteolipid protein gene (PLP) in a family with an unusual form of Pelizaeus-Merzbacher disease.

M. Hodes, M. E. Hodes, V. Pratt, 1997, American journal of medical genetics.

Analysis of region-specific library constructed by sequence-independent amplification of microdissected fragments surrounding weaver (wv) gene on mouse chromosome 16

B. Ghetti, M. E. Hodes, S. Dlouhy, 1994, Somatic Cell Genetics.

Adult-onset neurodegenerative disorder due to proteolipid protein gene mutation in the mother of a man with Pelizaeus-Merzbacher disease

M. Nance, M. Hodes, M. E. Hodes, 1996, Neurology.

In situ hybridization analysis of Girk2 expression in the developing central nervous system in normal and weaver mice.

B. Ghetti, S. Bayer, R. Piva, 1997, Journal of Neuropathology and Experimental Neurology.

Cloning a cDNA for carbonyl reductase (Cbr) from mouse cerebellum: murine genes that express cbr map to chromosomes 16 and 11.

B. Ghetti, M. E. Hodes, S. Dlouhy, 1996, Genomics.

cDNA approaches to isolation of the mouse mutant weaver gene

B. Ghetti, M. E. Hodes, L. Sangameswaran, 1994, Neurochemical Research.

Molecular characterization of a novel cDNA from murine cerebellum, developmental expression, and distribution in brain.

B. Ghetti, C. Kozak, M. E. Hodes, 1994, Brain research. Molecular brain research.