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Edward Ginns

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Ellen Sidransky; Mary E LaMarca; Edward I Ginns
Therapy for Gaucher disease: don't stop thinking about tomorrow.
Peter M Visscher; Chris S Haley; Henrik Ewald; Ole Mors; Janice A Egeland; B Thiel; Edward I Ginns; Walter Muir; D H R Blackwood
Joint multi-population analysis for genetic linkage of bipolar disorder or "wellness" to chromosome 4p.
Zheng Liu; Barry J Richmond; Elisabeth A Murray; Richard C Saunders; Sara Steenrod; Barbara K Stubblefield; Deidra M Montague; Edward I Ginns
DNA targeting of rhinal cortex D2 receptor protein reversibly blocks learning of cues that predict reward.

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All Publications

2007: Ellen Sidransky; Mary E LaMarca; Edward I Ginns
Therapy for Gaucher disease: don't stop thinking about tomorrow.
Molecular genetics and metabolism 2007;90(2):122-5.
2005: Peter M Visscher; Chris S Haley; Henrik Ewald; Ole Mors; Janice A Egeland; B Thiel; Edward I Ginns; Walter Muir; D H R Blackwood
Joint multi-population analysis for genetic linkage of bipolar disorder or "wellness" to chromosome 4p.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;133B(1):18-24.
2004: Zheng Liu; Barry J Richmond; Elisabeth A Murray; Richard C Saunders; Sara Steenrod; Barbara K Stubblefield; Deidra M Montague; Edward I Ginns
DNA targeting of rhinal cortex D2 receptor protein reversibly blocks learning of cues that predict reward.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(33):12336-41.
2002: M Galdzicka; Sujatha Patnala; M G Hirshman; J-F Cai; H Nitowsky; Janice A Egeland; Edward I Ginns
A new gene, EVC2, is mutated in Ellis-van Creveld syndrome.
Molecular genetics and metabolism 2002;77(4):291-5.
2002: Eduard Orvisky; Joseph Park; Mary E LaMarca; Edward I Ginns; Brian M Martin; Nahid Tayebi; Ellen Sidransky
Glucosylsphingosine accumulation in tissues from patients with Gaucher disease: correlation with phenotype and genotype.
Molecular genetics and metabolism 2002;76(4):262-70.
2002: Scott R Wersinger; Edward I Ginns; Anne-Marie O'Carroll; Stephen J Lolait; W Scott Young
Vasopressin V1b receptor knockout reduces aggressive behavior in male mice.
Molecular psychiatry 2002;7(9):975-84.
2001: Robert A Philibert; D Cheung; N Welsh; Patricia Damschroder-Williams; B Thiel; Edward I Ginns; Howard K Gershenfeld
Absence of a significant linkage between Na(+),K(+)-ATPase subunit (ATP1A3 and ATP1B3) genotypes and bipolar affective disorder in the old-order Amish.
American journal of medical genetics 2001;105(3):291-4.
2000: W L Yan; X Y Guan; Eric Green; Rob Nicolson; T K Yap; J Zhang; Leslie K Jacobsen; Donna Krasnewich; Sanjiv Kumra; Marge Lenane; Peter Gochman; Patricia Damschroder-Williams; LE Esterling; Robert T Long; Brian M Martin; Ellen Sidransky; Judy Rapoport; Edward I Ginns
Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21.
American journal of medical genetics 2000;96(6):749-53.
2000: Sylvie Fabrega; Patrick Durand; Patrice Codogno; Chantal Bauvy; C Delomenie; Bernard Henrissat; Brian M Martin; CE McKinney; Edward I Ginns; Jean-Paul Mornon; Pierre Lehn
Human glucocerebrosidase: heterologous expression of active site mutants in murine null cells.
Glycobiology 2000;10(11):1217-24.
2000: DL Stone; Nahid Tayebi; C Coble; Edward I Ginns; Ellen Sidransky
Cardiovascular fibrosis, hydrocephalus, ophthalmoplegia, and visceral involvement in an American child with Gaucher disease.
Journal of medical genetics 2000;37(11):E40.
2000: Eduard Orvisky; Ellen Sidransky; CE McKinney; Mary E LaMarca; R Samimi; Donna Krasnewich; Brian M Martin; Edward I Ginns
Glucosylsphingosine accumulation in mice and patients with type 2 Gaucher disease begins early in gestation.
Pediatric research 2000;48(2):233-7.
2000: DL Stone; Edward I Ginns; Donna Krasnewich; Ellen Sidransky
Life-threatening splenic hemorrhage in two patients with Gaucher disease.
American journal of hematology 2000;64(2):140-2.
2000: Robert A Philibert; SL Winfield; Harinder K Sandhu; Brian M Martin; Edward I Ginns
The structure and expression of the human neuroligin-3 gene.
Gene 2000;246(1-2):303-10.
1999: W Scott Young; Anna Iacangelo; X Z Luo; C King; K Duncan; Edward I Ginns
Transgenic expression of green fluorescent protein in mouse oxytocin neurones.
Journal of neuroendocrinology 1999;11(12):935-9.
1999: Robert A Philibert; SL Winfield; Patricia Damschroder-Williams; C Tengstrom; Brian M Martin; Edward I Ginns
The genomic structure and developmental expression patterns of the human OPA-containing gene (HOPA).
Human genetics 1999;105(1-2):174-8.
1999: Thomas V Fernandez; W L Yan; SD Hamburger; Judy Rapoport; Ann M Saunders; Mark B Schapiro; Edward I Ginns; Ellen Sidransky
Apolipoprotein E alleles in childhood-onset schizophrenia.
American journal of medical genetics 1999;88(2):211-3.
1999: EK Lau; Nahid Tayebi; Loring Ingraham; SL Winfield; V Koprivica; DL Stone; A Zimran; Edward I Ginns; Ellen Sidransky
Two novel polymorphic sequences in the glucocerebrosidase gene region enhance mutational screening and founder effect studies of patients with Gaucher disease.
Human genetics 1999;104(4):293-300.
1999: S Moriniere; C Saada; S Holbert; E Sidransky; A Galat; Edward I Ginns; Judy Rapoport; C Neri
Detection of polyglutamine expansion in a new acidic protein: a candidate for childhood onset schizophrenia?
Molecular psychiatry 1999;4(1):58-63.
1998: K Tenhunen; A Uusitalo; Taina Autti; Raimo Joensuu; M Kettunen; Risto A Kauppinen; S Ikonen; Mary E LaMarca; Matti Haltia; Edward I Ginns; Anu Jalanko; Leena Peltonen
Monitoring the CNS pathology in aspartylglucosaminuria mice.
Journal of neuropathology and experimental neurology 1998;57(12):1154-63.
1998: F Xavier Castellanos; E Lau; Nahid Tayebi; P Lee; R E Long; Jay Giedd; Wendy S Sharp; WL Marsh; James M Walter; SD Hamburger; Edward I Ginns; Judy Rapoport; Ellen Sidransky
Lack of an association between a dopamine-4 receptor polymorphism and attention-deficit/hyperactivity disorder: genetic and brain morphometric analyses.
Molecular psychiatry 1998;3(5):431-4.
1998: Catherine E Burgess; Kerstin Lindblad; Ellen Sidransky; Qiu-Ping Yuan; Robert T Long; TS Breschel; Christopher A Ross; Melvin G McInnis; P Lee; Edward I Ginns; Marge Lenane; Sanjiv Kumra; Leslie Jacobsen; Judy Rapoport; Martin Schalling
Large CAG/CTG repeats are associated with childhood-onset schizophrenia.
Molecular psychiatry 1998;3(4):321-7.
1998: Robert A Philibert; B H King; SL Winfield; Edwin H Cook; Y H Lee; Barbara K Stubblefield; Patricia Damschroder-Williams; C Dea; A Palotie; C Tengstrom; Brian M Martin; Edward I Ginns
Association of an X-chromosome dodecamer insertional variant allele with mental retardation.
Molecular psychiatry 1998;3(4):303-9.
1998: Ellen Sidransky; C Burgess; T Ikeuchi; Kerstin Lindblad; Robert T Long; Robert A Philibert; Judy Rapoport; Martin Schalling; S Tsuji; Edward I Ginns
A triplet repeat on 17q accounts for most expansions detected by the repeat-expansion-detection technique.
American journal of human genetics 1998;62(6):1548-51.
1998: Leslie K Jacobsen; BB Mittleman; Sanjiv Kumra; Marge Lenane; K C Barracchini; S Adams; TB Simonis; P R Lee; Robert T Long; Wendy S Sharp; Ellen Sidransky; Edward I Ginns; Judy Rapoport
HLA antigens in childhood onset schizophrenia.
Psychiatry research 1998;78(3):123-32.
1998: Donna Krasnewich; K Dietrich; L Bauer; Edward I Ginns; Ellen Sidransky; S Hill
Splenectomy in Gaucher disease: new management dilemmas.
Blood 1998;91(8):3085-7.
1998: W Yan; Leslie K Jacobsen; Donna Krasnewich; X Y Guan; Marge Lenane; S P Paul; H N Dalwadi; Heping Zhang; Robert T Long; Sanjiv Kumra; Brian M Martin; P J Scambler; Jeffrey M. Trent; Ellen Sidransky; Edward I Ginns; Judy Rapoport
Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired".
American journal of medical genetics 1998;81(1):41-3.
1998: Anu Jalanko; K Tenhunen; CE McKinney; Mary E LaMarca; Juhani Rapola; Taina Autti; Raimo Joensuu; Tuula Manninen; I Sipilä; S Ikonen; P Riekkinen; Edward I Ginns; Leena Peltonen
Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients.
Human molecular genetics 1998;7(2):265-72.
1998: Themis R Kyriakides; YH Zhu; L T Smith; Steven D Bain; Z Yang; M T Lin; K G Danielson; R V Iozzo; Mary E LaMarca; CE McKinney; Edward I Ginns; Paul Bornstein
Mice that lack thrombospondin 2 display connective tissue abnormalities that are associated with disordered collagen fibrillogenesis, an increased vascular density, and a bleeding diathesis.
The Journal of cell biology 1998;140(2):419-30.
1998: W Scott Young; E Shepard; AC DeVries; A Zimmer; Mary E LaMarca; Edward I Ginns; J Amico; R J Nelson; L Hennighausen; Kay-Uwe Wagner
Targeted reduction of oxytocin expression provides insights into its physiological roles.
Advances in experimental medicine and biology 1998;449():231-40.
1998: Robert A Philibert; N Horelli-Kuitunen; A S Robb; Y H Lee; Robert T Long; Patricia Damschroder-Williams; Brian M Martin; Miles B Brennan; A Palotie; Edward I Ginns
The characterization and sequence analysis of thirty CTG-repeat containing genomic cosmid clones.
European journal of human genetics : EJHG 1998;6(1):89-94.
1997: Ellen Sidransky; Edward I Ginns
Gaucher's disease: the best laid schemes of mice and men.
Baillière's clinical haematology 1997;10(4):725-37.
1997: Kay-Uwe Wagner; W Scott Young; X Liu; Edward I Ginns; M Li; Priscilla A Furth; Lothar Hennighausen
Oxytocin and milk removal are required for post-partum mammary-gland development.
Genes and function 1997;1(4):233-44.
1997: Ellen Sidransky; Edward I Ginns
Gaucher disease plus.
Journal of medical genetics 1997;34(10):876-7.
1997: SL Winfield; Nahid Tayebi; Brian M Martin; Edward I Ginns; Ellen Sidransky
Identification of three additional genes contiguous to the glucocerebrosidase locus on chromosome 1q21: implications for Gaucher disease.
Genome research 1997;7(10):1020-6.
1997: Robert A Philibert; Janice A Egeland; S M Paul; Edward I Ginns
The inheritance of bipolar affective disorder: abundant genes coming together.
Journal of affective disorders 1997;43(1):1-3.
1996: W Scott Young; E Shepard; J Amico; Lothar Hennighausen; Kay-Uwe Wagner; Mary E LaMarca; CE McKinney; Edward I Ginns
Deficiency in mouse oxytocin prevents milk ejection, but not fertility or parturition.
Journal of neuroendocrinology 1996;8(11):847-53.
1996: G L Long; SL Winfield; K W Adolph; Edward I Ginns; Paul Bornstein
Structure and organization of the human metaxin gene (MTX) and pseudogene.
Genomics 1996;33(2):177-84.
1996: Nahid Tayebi; J Herman; Edward I Ginns; Ellen Sidransky
Genotype D399N/R463C in a patient with type 3 Gaucher disease previously assigned genotype N370S/R463C.
Biochemical and molecular medicine 1996;57(2):149-51.
1996: Edward I Ginns; J Ott; Janice A Egeland; C R Allen; C S Fann; David L Pauls; J Weissenbachoff; J P Carulli; K M Falls; T P Keith; S M Paul
A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish.
Nature genetics 1996;12(4):431-5.
1996: Ellen Sidransky; Manige Fartasch; R E Lee; L A Metlay; S Abella; A Zimran; W Gao; P M Elias; Edward I Ginns; Walter M Holleran
Epidermal abnormalities may distinguish type 2 from type 1 and type 3 of Gaucher disease.
Pediatric research 1996;39(1):134-41.
1995: Ellen Sidransky; Nahid Tayebi; Edward I Ginns
Diagnosing Gaucher disease. Early recognition, implications for treatment, and genetic counseling.
Clinical pediatrics 1995;34(7):365-71.
1995: K W Adolph; G L Long; SL Winfield; Edward I Ginns; Paul Bornstein
Structure and organization of the human thrombospondin 3 gene (THBS3).
Genomics 1995;27(2):329-36.
1995: Paul Bornstein; CE McKinney; Mary E LaMarca; SL Winfield; T Shingu; S Devarayalu; H L Vos; Edward I Ginns
Metaxin, a gene contiguous to both thrombospondin 3 and glucocerebrosidase, is required for embryonic development in the mouse: implications for Gaucher disease.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(10):4547-51.
1995: Robert A Philibert; G A Hawkins; Patricia Damschroder-Williams; Barbara K Stubblefield; Brian M Martin; Edward I Ginns
Direct sequencing of trinucleotide repeats from cosmid genomic DNA template.
Analytical biochemistry 1995;225(2):372-4.
1994: Ellen Sidransky; A Bottler; Barbara K Stubblefield; Edward I Ginns
DNA mutational analysis of type 1 and type 3 Gaucher patients: how well do mutations predict phenotype?
Human mutation 1994;3(1):25-8.
1993: Ellen Sidransky; Edward I Ginns
Clinical heterogeneity among patients with Gaucher's disease.
JAMA : the journal of the American Medical Association 1993;269(9):1154-7.
1992: Ellen Sidransky; D M Sherer; Edward I Ginns
Gaucher disease in the neonate: a distinct Gaucher phenotype is analogous to a mouse model created by targeted disruption of the glucocerebrosidase gene.
Pediatric research 1992;32(4):494-8.
1992: Edward I Ginns; Janice A Egeland; C R Allen; David L Pauls; K Falls; T P Keith; S M Paul
Update on the search for DNA markers linked to manic-depressive illness in the Old Order Amish.
Journal of psychiatric research 1992;26(4):305-8.
1992: Ellen Sidransky; S Tsuji; Brian M Martin; Barbara K Stubblefield; Edward I Ginns
DNA mutation analysis of Gaucher patients.
American journal of medical genetics 1992;42(3):331-6.
1992: Ellen Sidransky; S Tsuji; Barbara K Stubblefield; J Currie; E J FitzGibbon; Edward I Ginns
Gaucher patients with oculomotor abnormalities do not have a unique genotype.
Clinical genetics 1992;41(1):1-5.
1991: P Montpied; Edward I Ginns; Brian M Martin; D Roca; D H Farb; S M Paul
gamma-Aminobutyric acid (GABA) induces a receptor-mediated reduction in GABAA receptor alpha subunit messenger RNAs in embryonic chick neurons in culture.
The Journal of biological chemistry 1991;266(10):6011-4.
1991: P Montpied; A Leslie Morrow; J W Karanian; Edward I Ginns; Brian M Martin; S M Paul
Prolonged ethanol inhalation decreases gamma-aminobutyric acidA receptor alpha subunit mRNAs in the rat cerebral cortex.
Molecular pharmacology 1991;39(2):157-63.
1989: P Montpied; Edward I Ginns; Brian M Martin; D Stetler; Anne-Marie O'Carroll; S J Lolait; L C Mahan; S M Paul
Multiple GABAA receptor alpha subunit mRNAs revealed by developmental and regional expression in rat, chicken and human brain.
FEBS letters 1989;258(1):94-8.
1989: John R Kelsoe; Edward I Ginns; Janice A Egeland; Daniela S Gerhard; A M Goldstein; S J Bale; David L Pauls; Robert T Long; K K Kidd; G Conte
Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish.
Nature 1989;342(6247):238-43.
1989: Brian M Martin; Ellen Sidransky; Edward I Ginns
Gaucher's disease: advances and challenges.
Advances in pediatrics 1989;36():277-306.
1988: P Montpied; Brian M Martin; S L Cottingham; Barbara K Stubblefield; Edward I Ginns; S M Paul
Regional distribution of the GABAA/benzodiazepine receptor (alpha subunit) mRNA in rat brain.
Journal of neurochemistry 1988;51(5):1651-4.
1988: John R Kelsoe; Barbara K Stubblefield; Edward I Ginns
Human tyrosine hydroxylase (TH) genomic fragment (pHGTH4) identifies a PstI polymorphism.
Nucleic acids research 1988;16(15):7760.
1988: Edward I Ginns; M Rehavi; Brian M Martin; M Weller; Karen L O'Malley; Mary E LaMarca; C G McAllister; S M Paul
Expression of human tyrosine hydroxylase cDNA in invertebrate cells using a baculovirus vector.
The Journal of biological chemistry 1988;263(15):7406-10.
1988: S Tsuji; Brian M Martin; J A Barranger; Barbara K Stubblefield; Mary E LaMarca; Edward I Ginns
Genetic heterogeneity in type 1 Gaucher disease: multiple genotypes in Ashkenazic and non-Ashkenazic individuals.
Proceedings of the National Academy of Sciences of the United States of America 1988;85(7):2349-52.
1988: Brian M Martin; S Tsuji; Mary E LaMarca; K Maysak; W Eliason; Edward I Ginns
Glycosylation and processing of high levels of active human glucocerebrosidase in invertebrate cells using a baculovirus expression vector.
DNA (Mary Ann Liebert, Inc.) 1988;7(2):99-106.
1988: V Ionasescu; T Burns; R Ionasescu; Charles C Searby; Edward I Ginns
Linkage between the loci for autosomal dominant Charcot-Marie-Tooth neuropathy type 1 and human glucocerebrosidase.
Cytogenetics and cell genetics 1988;47(3):173-4.
1987: Y S Kim; J W Thomas; Niranjala J K Tillakaratne; P Montpied; P D Suzdak; C Banner; Edward I Ginns; Allan J Tobin; S M Paul
Glutamic acid decarboxylase mRNA in rat brain: regional distribution and effects of intrastriatal kainic acid.
Brain research 1987;427(1):77-82.
1987: S Tsuji; Brian M Martin; D C Kaslow; Barbara R Migeon; P V Choudary; B K Stubbleflied; J A Mayor; G J Murray; J A Barranger; Edward I Ginns
Signal sequence and DNA-mediated expression of human lysosomal alpha-galactosidase A.
European journal of biochemistry / FEBS 1987;165(2):275-80.
1987: Donald E Schmechel; P J Marangos; Brian M Martin; SL Winfield; D S Burkhart; Allen D Roses; Edward I Ginns
Localization of neuron-specific enolase (NSE) mRNA in human brain.
Neuroscience letters 1987;76(2):233-8.
1987: S Tsuji; P V Choudary; Brian M Martin; Barbara K Stubblefield; J A Mayor; J A Barranger; Edward I Ginns
A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's disease.
The New England journal of medicine 1987;316(10):570-5.
1986: P V Choudary; J A Barranger; S Tsuji; J Mayor; Mary E LaMarca; C L Cepko; R C Mulligan; Edward I Ginns
Retrovirus-mediated transfer of the human glucocerebrosidase gene to Gaucher fibroblasts.
Molecular biology & medicine 1986;3(3):293-9.
1986: S Tsuji; P V Choudary; Brian M Martin; SL Winfield; J A Barranger; Edward I Ginns
Nucleotide sequence of cDNA containing the complete coding sequence for human lysosomal glucocerebrosidase.
The Journal of biological chemistry 1986;261(1):50-3.
1986: P V Choudary; S Tsuji; Brian M Martin; B C Guild; R C Mulligan; G J Murray; J A Barranger; Edward I Ginns
The molecular biology of Gaucher disease and the potential for gene therapy.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 2():1047-52.
1985: Edward I Ginns; P V Choudary; S Tsuji; B Martin; Barbara K Stubblefield; J Sawyer; John Hozier; J A Barranger
Gene mapping and leader polypeptide sequence of human glucocerebrosidase: implications for Gaucher disease.
Proceedings of the National Academy of Sciences of the United States of America 1985;82(20):7101-5.
1984: Edward I Ginns; P V Choudary; Brian M Martin; SL Winfield; Barbara K Stubblefield; J Mayor; D Merkle-Lehman; G J Murray; L A Bowers; J A Barranger
Isolation of cDNA clones for human beta-glucocerebrosidase using the lambda gt11 expression system.
Biochemical and biophysical research communications 1984;123(2):574-80.