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Mihael Polymeropoulos
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17
Dehejia, AM
14
Leroy, E
11
Lavedan, Christian
10
Nussbaum, Robert
8
Francomano, Clair
5
Athanassiadou, Aglaia
5
Trent, Jeffry
5
Buchholtz, Stephanie
4
Biddison, William
4
Boyer, RL
4
Becker, KG
4
Canning, RD
4
Dressman, Marlene
4
Drew, PD
4
Dutra, Amalia
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All Publications
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2009: Volpi S; Heaton C; Mack K; Hamilton J B; Lannan R; Wolfgang C D; Licamele L; Polymeropoulos M H; Lavedan C
Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia.
Molecular psychiatry 2009;14(11):1024-31.
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2009: Lavedan C; Licamele L; Volpi S; Hamilton J; Heaton C; Mack K; Lannan R; Thompson A; Wolfgang C D; Polymeropoulos M H
Association of the NPAS3 gene and five other loci with response to the antipsychotic iloperidone identified in a whole genome association study.
Molecular psychiatry 2009;14(8):804-19.
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2009: Polymeropoulos Mihael H; Licamele Louis; Volpi Simona; Mack Kendra; Mitkus Shruti N; Carstea Eugene D; Getoor Lise; Thompson Andrew; Lavedan Christian
Common effect of antipsychotics on the biosynthesis and regulation of fatty acids and cholesterol supports a key role of lipid homeostasis in schizophrenia.
Schizophrenia research 2009;108(1-3):134-42.
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2009: Rajaratnam Shantha Mw; Polymeropoulos Mihael H; Fisher Dennis M; Roth Thomas; Scott Christin; Birznieks Gunther; Klerman Elizabeth B
Melatonin agonist tasimelteon (VEC-162) for transient insomnia after sleep-time shift: two randomised controlled multicentre trials.
Lancet 2009;373(9662):482-91.
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2008: Weiden Peter J; Cutler Andrew J; Polymeropoulos Mihael H; Wolfgang Curt D
Safety profile of iloperidone: a pooled analysis of 6-week acute-phase pivotal trials.
Journal of clinical psychopharmacology 2008;28(2 Suppl 1):S12-9.
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2008: Lavedan Christian; Volpi Simona; Polymeropoulos Mihael H; Wolfgang Curt D
Effect of a ciliary neurotrophic factor polymorphism on schizophrenia symptom improvement in an iloperidone clinical trial.
Pharmacogenomics 2008;9(3):289-301.
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2005: Yamaguchi Keiji; Cochran Elizabeth J; Murrell Jill R; Polymeropoulos Mihael H; Shannon Kathleen M; Crowther R Anthony; Goedert Michel; Ghetti Bernardino
Abundant neuritic inclusions and microvacuolar changes in a case of diffuse Lewy body disease with the A53T mutation in the alpha-synuclein gene.
Acta neuropathologica 2005;110(3):298-305.
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2004: Dressman Marlene A; Malinowski Rachel; McLean Lee Anne; Gathmann Insa; Capdeville Renaud; Hensley Martee; Polymeropoulos Mihael H;
Correlation of major cytogenetic response with a pharmacogenetic marker in chronic myeloid leukemia patients treated with imatinib (STI571).
Clinical cancer research : an official journal of the American Association for Cancer Research 2004;10(7):2265-71.
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2004: McLean Lee Anne; Gathmann Insa; Capdeville Renaud; Polymeropoulos Mihael H; Dressman Marlene
Pharmacogenomic analysis of cytogenetic response in chronic myeloid leukemia patients treated with imatinib.
Clinical cancer research : an official journal of the American Association for Cancer Research 2004;10(1 Pt 1):155-65.
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2003: Dressman Marlene A; Baras Alex; Malinowski Rachel; Alvis Lisa B; Kwon Irene; Walz Thomas M; Polymeropoulos Mihael H
Gene expression profiling detects gene amplification and differentiates tumor types in breast cancer.
Cancer research 2003;63(9):2194-9.
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2002: Lavedan Christian; Buchholtz Stephanie; Nussbaum Robert L; Albin Roger L; Polymeropoulos Mihael H
A mutation in the human neurofilament M gene in Parkinson's disease that suggests a role for the cytoskeleton in neuronal degeneration.
Neuroscience letters 2002;322(1):57-61.
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2001: Teive H A; Raskin S; Iwamoto F M; Germiniani F M; Baran M H; Werneck L C; Allan N; Quagliato E; Leroy E; Ide S E; Polymeropoulos M H
The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease.
Arquivos de neuro-psiquiatria 2001;59(3-B):722-4.
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2001: Papapetropoulos S; Paschalis C; Athanassiadou A; Papadimitriou A; Ellul J; Polymeropoulos M H; Papapetropoulos T
Clinical phenotype in patients with alpha-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease.
Journal of neurology, neurosurgery, and psychiatry 2001;70(5):662-5.
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2001: Torres R; Leroy E; Hu X; Katrivanou A; Gourzis P; Papachatzopoulou A; Athanassiadou A; Beratis S; Collier D; Polymeropoulos M H
Mutation screening of the Wolfram syndrome gene in psychiatric patients.
Molecular psychiatry 2001;6(1):39-43.
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2001: Touchman J W; Dehejia A; Chiba-Falek O; Cabin D E; Schwartz J R; Orrison B M; Polymeropoulos M H; Nussbaum R L
Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element.
Genome research 2001;11(1):78-86.
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2001: Dressman M A; Walz T M; Lavedan C; Barnes L; Buchholtz S; Kwon I; Ellis M J; Polymeropoulos M H
Genes that co-cluster with estrogen receptor alpha in microarray analysis of breast biopsies.
The pharmacogenomics journal 2001;1(2):135-41.
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2000: Wintermeyer P; Krüger R; Kuhn W; Müller T; Woitalla D; Berg D; Becker G; Leroy E; Polymeropoulos M; Berger K; Przuntek H; Schöls L; Epplen J T; Riess O
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients.
Neuroreport 2000;11(10):2079-82.
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2000: Charles V; Mezey E; Reddy P H; Dehejia A; Young T A; Polymeropoulos M H; Brownstein M J; Tagle D A
Alpha-synuclein immunoreactivity of huntingtin polyglutamine aggregates in striatum and cortex of Huntington's disease patients and transgenic mouse models.
Neuroscience letters 2000;289(1):29-32.
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2000: Ruiz-Perez V L; Ide S E; Strom T M; Lorenz B; Wilson D; Woods K; King L; Francomano C; Freisinger P; Spranger S; Marino B; Dallapiccola B; Wright M; Meitinger T; Polymeropoulos M H; Goodship J
Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis.
Nature genetics 2000;24(3):283-6.
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2000: Polymeropoulos M H
Genetics of Parkinson's disease.
Annals of the New York Academy of Sciences 2000;920():28-32.
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1999: Piétu G; Eveno E; Soury-Segurens B; Fayein N A; Mariage-Samson R; Matingou C; Leroy E; Dechesne C; Krieger S; Ansorge W; Reguigne-Arnould I; Cox D; Dehejia A; Polymeropoulos M H; Devignes M D; Auffray C
The genexpress IMAGE knowledge base of the human muscle transcriptome: a resource of structural, functional, and positional candidate genes for muscle physiology and pathologies.
Genome research 1999;9(12):1313-20.
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1999: Hardy C; Khanim F; Torres R; Scott-Brown M; Seller A; Poulton J; Collier D; Kirk J; Polymeropoulos M; Latif F; Barrett T
Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1.
American journal of human genetics 1999;65(5):1279-90.
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1999: Torres R; Ide S E; Dehejia A; Baras A; Polymeropoulos M H
Genomic structure and localization of the human protein phosphatase 2A BRgamma regulatory subunit.
DNA research : an international journal for rapid publication of reports on genes and genomes 1999;6(5):323-7.
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1999: Athanassiadou A; Voutsinas G; Psiouri L; Leroy E; Polymeropoulos M H; Ilias A; Maniatis G M; Papapetropoulos T
Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein.
American journal of human genetics 1999;65(2):555-8.
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1998: Lavedan C; Buchholtz S; Auburger G; Albin R L; Athanassiadou A; Blancato J; Burguera J A; Ferrell R E; Kostic V; Leroy E; Leube B; Mota-Vieira L; Papapetropoulos T; Pericak-Vance M A; Pinkus J; Scott W K; Ulm G; Vasconcelos J; Vilchez J J; Nussbaum R L; Polymeropoulos M H
Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease.
DNA research : an international journal for rapid publication of reports on genes and genomes 1998;5(6):401-2.
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1998: Leroy E; Boyer R; Polymeropoulos M H
Intron-exon structure of ubiquitin c-terminal hydrolase-L1.
DNA research : an international journal for rapid publication of reports on genes and genomes 1998;5(6):397-400.
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1998: Torres R; Polymeropoulos M H
Genomic organization and localization of the human CRMP-1 gene.
DNA research : an international journal for rapid publication of reports on genes and genomes 1998;5(6):393-5.
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1998: Gruber S B; Entius M M; Petersen G M; Laken S J; Longo P A; Boyer R; Levin A M; Mujumdar U J; Trent J M; Kinzler K W; Vogelstein B; Hamilton S R; Polymeropoulos M H; Offerhaus G J; Giardiello F M
Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome.
Cancer research 1998;58(23):5267-70.
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1998: Mezey E; Dehejia A M; Harta G; Tresser N; Suchy S F; Nussbaum R L; Brownstein M J; Polymeropoulos M H
Alpha synuclein is present in Lewy bodies in sporadic Parkinson's disease.
Molecular psychiatry 1998;3(6):493-9.
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1998: Polymeropoulos M H
Autosomal dominant Parkinson's disease.
Journal of neurology 1998;245(11 Suppl 3):P1-3.
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1998: Lavedan C; Leroy E; Torres R; Dehejia A; Dutra A; Buchholtz S; Nussbaum R L; Polymeropoulos M H
Genomic organization and expression of the human beta-synuclein gene (SNCB).
Genomics 1998;54(1):173-5.
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1998: Leroy E; Anastasopoulos D; Konitsiotis S; Lavedan C; Polymeropoulos M H
Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's disease.
Human genetics 1998;103(4):424-7.
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1998: Deloukas P; Schuler G D; Gyapay G; Beasley E M; Soderlund C; Rodriguez-Tomé P; Hui L; Matise T C; McKusick K B; Beckmann J S; Bentolila S; Bihoreau M; Birren B B; Browne J; Butler A; Castle A B; Chiannilkulchai N; Clee C; Day P J; Dehejia A; Dibling T; Drouot N; Duprat S; Fizames C; Fox S; Gelling S; Green L; Harrison P; Hocking R; Holloway E; Hunt S; Keil S; Lijnzaad P; Louis-Dit-Sully C; Ma J; Mendis A; Miller J; Morissette J; Muselet D; Nusbaum H C; Peck A; Rozen S; Simon D; Slonim D K; Staples R; Stein L D; Stewart E A; Suchard M A; Thangarajah T; Vega-Czarny N; Webber C; Wu X; Hudson J; Auffray C; Nomura N; Sikela J M; Polymeropoulos M H; James M R; Lander E S; Hudson T J; Myers R M; Cox D R; Weissenbach J; Boguski M S; Bentley D R
A physical map of 30,000 human genes.
Science (New York, N.Y.) 1998;282(5389):744-6.
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1998: Leroy E; Boyer R; Auburger G; Leube B; Ulm G; Mezey E; Harta G; Brownstein M J; Jonnalagada S; Chernova T; Dehejia A; Lavedan C; Gasser T; Steinbach P J; Wilkinson K D; Polymeropoulos M H
The ubiquitin pathway in Parkinson's disease.
Nature 1998;395(6701):451-2.
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1998: Polymeropoulos M H
Autosomal dominant Parkinson's disease and alpha-synuclein.
Annals of neurology 1998;44(3 Suppl 1):S63-4.
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1998: Patel S B; Salen G; Hidaka H; Kwiterovich P O; Stalenhoef A F; Miettinen T A; Grundy S M; Lee M H; Rubenstein J S; Polymeropoulos M H; Brownstein M J
Mapping a gene involved in regulating dietary cholesterol absorption. The sitosterolemia locus is found at chromosome 2p21.
The Journal of clinical investigation 1998;102(5):1041-4.
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1998: Knutsen T; Mickley L A; Ried T; Green E D; du Manoir S; Schröck E; Macville M; Ning Y; Robey R; Polymeropoulos M; Torres R; Fojo T
Cytogenetic and molecular characterization of random chromosomal rearrangements activating the drug resistance gene, MDR1/P-glycoprotein, in drug-selected cell lines and patients with drug refractory ALL.
Genes, chromosomes & cancer 1998;23(1):44-54.
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1998: Lavedan C; Leroy E; Dehejia A; Buchholtz S; Dutra A; Nussbaum R L; Polymeropoulos M H
Identification, localization and characterization of the human gamma-synuclein gene.
Human genetics 1998;103(1):106-12.
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1998: Mezey E; Dehejia A; Harta G; Papp M I; Polymeropoulos M H; Brownstein M J
Alpha synuclein in neurodegenerative disorders: murderer or accomplice?
Nature medicine 1998;4(7):755-7.
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1998: Stumpo D J; Eddy R L; Haley L L; Sait S; Shows T B; Lai W S; Young W S; Speer M C; Dehejia A; Polymeropoulos M; Blackshear P J
Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein: identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects.
Genomics 1998;49(2):253-64.
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1998: Lavedan C; Dehejia A; Pike B; Dutra A; Leroy E; Ide S E; Root H; Rubenstein J; Boyer R L; Chandrasekharappa S; Makalowska I; Nussbaum R L; Polymeropoulos M H
Contig map of the Parkinson's disease region on 4q21-q23.
DNA research : an international journal for rapid publication of reports on genes and genomes 1998;5(1):19-23.
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1998: Annabi B; Hiraiwa H; Mansfield B C; Lei K J; Ubagai T; Polymeropoulos M H; Moses S W; Parvari R; Hershkovitz E; Mandel H; Fryman M; Chou J Y
The gene for glycogen-storage disease type 1b maps to chromosome 11q23.
American journal of human genetics 1998;62(2):400-5.
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1998: Swift R G; Polymeropoulos M H; Torres R; Swift M
Predisposition of Wolfram syndrome heterozygotes to psychiatric illness.
Molecular psychiatry 1998;3(1):86-91.
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1997: Drew P D; Gado A M; Canning R D; Nagle J W; Dehejia A M; Polymeropoulos M H; Biddison W E; Jacobson S; Becker K G
C2H2-546: a zinc finger protein differentially expressed in HTLV-1 infected T cells.
Journal of neurovirology 1997;3(6):455-9.
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1997: Becker K G; Lee I J; Nagle J W; Canning R D; Gado A M; Torres R; Polymeropoulos M H; Massa P T; Biddison W E; Drew P D
C2H2-171: a novel human cDNA representing a developmentally regulated POZ domain/zinc finger protein preferentially expressed in brain.
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 1997;15(7):891-9.
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1997: Johnson M R; Wilkin D J; Vos H L; Ortiz de Luna R I; Dehejia A M; Polymeropoulos M H; Francomano C A
Characterization of the human extracellular matrix protein 1 gene on chromosome 1q21.
Matrix biology : journal of the International Society for Matrix Biology 1997;16(5):289-92.
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1997: Luo G; Leroy E; Kozak C A; Polymeropoulos M H; Horowits R
Mapping of the gene (NRAP) encoding N-RAP in the mouse and human genomes.
Genomics 1997;45(1):229-32.
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1997: Carstea E D; Morris J A; Coleman K G; Loftus S K; Zhang D; Cummings C; Gu J; Rosenfeld M A; Pavan W J; Krizman D B; Nagle J; Polymeropoulos M H; Sturley S L; Ioannou Y A; Higgins M E; Comly M; Cooney A; Brown A; Kaneski C R; Blanchette-Mackie E J; Dwyer N K; Neufeld E B; Chang T Y; Liscum L; Strauss J F; Ohno K; Zeigler M; Carmi R; Sokol J; Markie D; O'Neill R R; van Diggelen O P; Elleder M; Patterson M C; Brady R O; Vanier M T; Pentchev P G; Tagle D A
Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis.
Science (New York, N.Y.) 1997;277(5323):228-31.
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1997: Polymeropoulos M H; Lavedan C; Leroy E; Ide S E; Dehejia A; Dutra A; Pike B; Root H; Rubenstein J; Boyer R; Stenroos E S; Chandrasekharappa S; Athanassiadou A; Papapetropoulos T; Johnson W G; Lazzarini A M; Duvoisin R C; Di Iorio G; Golbe L I; Nussbaum R L
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
Science (New York, N.Y.) 1997;276(5321):2045-7.
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1997: Becker K G; Nagle J W; Canning R D; Dehejia A M; Polymeropoulos M H; Gado A M; Biddison W E; Drew P D
Molecular cloning and mapping of a novel human KRAB domain-containing C2H2-type zinc finger to chromosome 7q36.1.
Genomics 1997;41(3):502-4.
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1997: Higgins J J; Pho L T; Ide S E; Nee L E; Polymeropoulos M H
Evidence for a new spinocerebellar ataxia locus.
Movement disorders : official journal of the Movement Disorder Society 1997;12(3):412-7.
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1997: Becker K G; Canning R D; Nagle J W; Dehejia A M; Polymeropoulos M H; Lee I J; Gado A M; Biddison W E; Drew P D
Molecular cloning and mapping of a novel developmentally regulated human C2H2-type zinc finger.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(4):287-9.
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1997: Polymeropoulos M H; Hurko O; Hsu F; Rubenstein J; Basnet S; Lane K; Dietz H; Spetzler R F; Rigamonti D
Linkage of the locus for cerebral cavernous hemangiomas to human chromosome 7q in four families of Mexican-American descent.
Neurology 1997;48(3):752-7.
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1997: Higgins J J; Ide S E; Oghalai J S; Polymeropoulos M H
Lack of mutations in the biotin-binding region of the pyruvate carboxylase (PC) gene in a family with partial PC deficiency.
Clinical biochemistry 1997;30(1):79-81.
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1997: Gracia E; Ray M E; Polymeropoulos M H; Dehejia A; Meltzer P S; Trent J M
Isolation of chromosome-specific ESTs by microdissection-mediated cDNA capture.
Genome research 1997;7(2):100-7.
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1997: Freedman R; Coon H; Myles-Worsley M; Orr-Urtreger A; Olincy A; Davis A; Polymeropoulos M; Holik J; Hopkins J; Hoff M; Rosenthal J; Waldo M C; Reimherr F; Wender P; Yaw J; Young D A; Breese C R; Adams C; Patterson D; Adler L E; Kruglyak L; Leonard S; Byerley W
Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(2):587-92.
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1997: Nussbaum R L; Polymeropoulos M H
Genetics of Parkinson's disease.
Human molecular genetics 1997;6(10):1687-91.
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1996: Polymeropoulos M H; Schaffer A A
Scanning the genome with 1772 microsatellite markers in search of a bipolar disorder susceptibility gene.
Molecular psychiatry 1996;1(5):404-7.
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1996: Polymeropoulos M H; Ide S E; Becker K; Naylor S L
Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22.
Cancer genetics and cytogenetics 1996;92(1):46-9.
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1996: Polymeropoulos M H; Ide S E; Magyari T; Francomano C A
Brachydactyly type C gene maps to human chromsome 12q24.
Genomics 1996;38(1):45-50.
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1996: Johnson M R; Polymeropoulos M H; Vos H L; Ortiz de Luna R I; Francomano C A
A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosis.
Genome research 1996;6(11):1050-5.
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1996: Polymeropoulos M H; Higgins J J; Golbe L I; Johnson W G; Ide S E; Di Iorio G; Sanges G; Stenroos E S; Pho L T; Schaffer A A; Lazzarini A M; Nussbaum R L; Duvoisin R C
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23.
Science (New York, N.Y.) 1996;274(5290):1197-9.
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1996: Ide S E; Ortiz de Luna R I; Francomano C A; Polymeropoulos M H
Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the Amish.
Human genetics 1996;98(5):572-5.
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1996: Schuler G D; Boguski M S; Stewart E A; Stein L D; Gyapay G; Rice K; White R E; Rodriguez-Tomé P; Aggarwal A; Bajorek E; Bentolila S; Birren B B; Butler A; Castle A B; Chiannilkulchai N; Chu A; Clee C; Cowles S; Day P J; Dibling T; Drouot N; Dunham I; Duprat S; East C; Edwards C; Fan J B; Fang N; Fizames C; Garrett C; Green L; Hadley D; Harris M; Harrison P; Brady S; Hicks A; Holloway E; Hui L; Hussain S; Louis-Dit-Sully C; Ma J; MacGilvery A; Mader C; Maratukulam A; Matise T C; McKusick K B; Morissette J; Mungall A; Muselet D; Nusbaum H C; Page D C; Peck A; Perkins S; Piercy M; Qin F; Quackenbush J; Ranby S; Reif T; Rozen S; Sanders C; She X; Silva J; Slonim D K; Soderlund C; Sun W L; Tabar P; Thangarajah T; Vega-Czarny N; Vollrath D; Voyticky S; Wilmer T; Wu X; Adams M D; Auffray C; Walter N A; Brandon R; Dehejia A; Goodfellow P N; Houlgatte R; Hudson J R; Ide S E; Iorio K R; Lee W Y; Seki N; Nagase T; Ishikawa K; Nomura N; Phillips C; Polymeropoulos M H; Sandusky M; Schmitt K; Berry R; Swanson K; Torres R; Venter J C; Sikela J M; Beckmann J S; Weissenbach J; Myers R M; Cox D R; James M R; Bentley D; Deloukas P; Lander E S; Hudson T J
A gene map of the human genome.
Science (New York, N.Y.) 1996;274(5287):540-6.
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1996: McDowell G; Isogai T; Tanigami A; Hazelwood S; Ledbetter D; Polymeropoulos M H; Lichter-Konecki U; Konecki D; Town M M; Van't Hoff W V; Weissenbach J; Gahl W A
Fine mapping of the cystinosis gene using an integrated genetic and physical map of a region within human chromosome band 17p13.
Biochemical and molecular medicine 1996;58(2):135-41.
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1996: Zinovieva R D; Duncan M K; Johnson T R; Torres R; Polymeropoulos M H; Tomarev S I
Structure and chromosomal localization of the human homeobox gene Prox 1.
Genomics 1996;35(3):517-22.
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1996: Lechleider R J; de Caestecker M P; Dehejia A; Polymeropoulos M H; Roberts A B
Serine phosphorylation, chromosomal localization, and transforming growth factor-beta signal transduction by human bsp-1.
The Journal of biological chemistry 1996;271(30):17617-20.
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1996: Polymeropoulos M H; Ide S E; Wright M; Goodship J; Weissenbach J; Pyeritz R E; Da Silva E O; Ortiz De Luna R I; Francomano C A
The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16.
Genomics 1996;35(1):1-5.
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1996: Lennon G; Auffray C; Polymeropoulos M; Soares M B
The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression.
Genomics 1996;33(1):151-2.
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1996: Brinkmann U; Gallo M; Polymeropoulos M H; Pastan I
The human CAS (cellular apoptosis susceptibility) gene mapping on chromosome 20q13 is amplified in BT474 breast cancer cells and part of aberrant chromosomes in breast and colon cancer cell lines.
Genome research 1996;6(3):187-94.
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1996: Gill M; Vallada H; Collier D; Sham P; Holmans P; Murray R; McGuffin P; Nanko S; Owen M; Antonarakis S; Housman D; Kazazian H; Nestadt G; Pulver A E; Straub R E; MacLean C J; Walsh D; Kendler K S; DeLisi L; Polymeropoulos M; Coon H; Byerley W; Lofthouse R; Gershon E; Read C M
A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).
American journal of medical genetics 1996;67(1):40-5.
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1996: Lee H Y; Murata J; Clair T; Polymeropoulos M H; Torres R; Manrow R E; Liotta L A; Stracke M L
Cloning, chromosomal localization, and tissue expression of autotaxin from human teratocarcinoma cells.
Biochemical and biophysical research communications 1996;218(3):714-9.
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1996: Higgins J J; Nee L E; Vasconcelos O; Ide S E; Lavedan C; Goldfarb L G; Polymeropoulos M H
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease.
Neurology 1996;46(1):208-13.
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1995: Polymeropoulos M H; Ide S; Soares M B; Lennon G G
Sequence characterization and genetic mapping of the human VSNL1 gene, a homologue of the rat visinin-like peptide RNVP1.
Genomics 1995;29(1):273-5.
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1995: Polymeropoulos M H; Torres R; Yanovski J A; Chandrasekharappa S C; Ledbetter D H
The human corticotropin-releasing factor receptor (CRHR) gene maps to chromosome 17q12-q22.
Genomics 1995;28(1):123-4.
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1995: Polymeropoulos M H; Ortiz De Luna R I; Ide S E; Torres R; Rubenstein J; Francomano C A
The gene for pycnodysostosis maps to human chromosome 1cen-q21.
Nature genetics 1995;10(2):238-9.
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1995: Polymeropoulos M H; Poush J; Rubenstein J R; Francomano C A
Localization of the gene (SYM1) for proximal symphalangism to human chromosome 17q21-q22.
Genomics 1995;27(2):225-9.
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1995: Pappas G J; Polymeropoulos M H; Boyle J M; Trent J M
Regional assignment by hybrid mapping of 36 expressed sequence tags (ESTs) on human chromosome 6.
Genomics 1995;25(1):124-9.
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1995: Slorach E M; Polymeropoulos M H; Evans K L; Seawright A; Fletcher J M; Porteous D J; Brookes A J
Regional localisation of 19 brain expressed sequence tags to human chromosome 11 using PCR amplification of somatic cell hybrid DNAs.
Cytogenetics and cell genetics 1995;70(1-2):71-5.
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1995: Zimonjic D B; Rezanka L J; Evans C H; Polymeropoulos M H; Trent J M; Popescu N C
Mapping of the immune interferon gamma gene (IFNG) to chromosome band 12q14 by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1995;71(3):247-8.
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1994: Gerken S; Fish K; Uyar D; Polymeropoulos M H; Bradley P; White R; Overhauser J; Silverman G A
Integration of 28 STSs into the physical map of human chromosome 18.
Genomics 1994;24(3):612-3.
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1994: Yano K; Hidaka A; Saji M; Polymeropoulos M H; Okuno A; Kohn L D; Cutler G B
A sporadic case of male-limited precocious puberty has the same constitutively activating point mutation in luteinizing hormone/choriogonadotropin receptor gene as familial cases.
The Journal of clinical endocrinology and metabolism 1994;79(6):1818-23.
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1994: Polymeropoulos M H; Swift R G; Swift M
Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4.
Nature genetics 1994;8(1):95-7.
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1994: Heinzmann C; Kojis T L; Gonzalez P; Rao P V; Zigler J S; Polymeropoulos M H; Klisak I; Sparkes R S; Mohandas T; Bateman J B
Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphisms.
Genomics 1994;23(2):403-7.
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1994: Polymeropoulos M H; Coon H; Byerley W; Gershon E S; Goldin L; Crow T J; Rubenstein J; Hoff M; Holik J; Smith A M
Search for a schizophrenia susceptibility locus on human chromosome 22.
American journal of medical genetics 1994;54(2):93-9.
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1994: Meezaman D; Charles P; Daskal E; Polymeropoulos M H; Martin B M; Rose M C
Cloning and analysis of cDNA encoding a major airway glycoprotein, human tracheobronchial mucin (MUC5).
The Journal of biological chemistry 1994;269(17):12932-9.
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1993: Polymeropoulos M H; Xiao H; Sikela J M; Adams M; Venter J C; Merril C R
Chromosomal distribution of 320 genes from a brain cDNA library.
Nature genetics 1993;4(4):381-6.
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1993: Zullo S; Kennedy J L; Gelernter J; Polymeropoulos M H; Tallini G; Pakstis A J; Shapiro M B; Merril C R; Kidd K K
Eliminating mitochondrial DNA competition for nuclear DNA primers.
PCR methods and applications 1993;3(1):39-45.
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1993: Polymeropoulos M H; Xiao H; Torrey E F; DeLisi L E; Crow T; Merril C R
Search for a genetic event in monozygotic twins discordant for schizophrenia.
Psychiatry research 1993;48(1):27-36.
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1993: Xiao H; Ide S E; Merril C R; Polymeropoulos M H
Dinucleotide repeat polymorphism at the D11S982E locus.
Human molecular genetics 1993;2(7):1081.
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1993: Polymeropoulos M H; Xiao H; Ide S E; Merril C R
Dinucleotide repeat polymorphism at the D14S99E locus.
Human molecular genetics 1993;2(4):490.
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1993: Carstea E D; Polymeropoulos M H; Parker C C; Detera-Wadleigh S D; O'Neill R R; Patterson M C; Goldin E; Xiao H; Straub R E; Vanier M T
Linkage of Niemann-Pick disease type C to human chromosome 18.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(5):2002-4.
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1993: Wilkie P J; Polymeropoulos M H; Trent J M; Small K W; Weber J L
Genetic and physical map of 11 short tandem repeat polymorphisms on human chromosome 6.
Genomics 1993;15(1):225-7.
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1992: Polymeropoulos M H; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the D18S74E locus.
Human molecular genetics 1992;1(9):779.
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1992: Khan A S; Wilcox A S; Polymeropoulos M H; Hopkins J A; Stevens T J; Robinson M; Orpana A K; Sikela J M
Single pass sequencing and physical and genetic mapping of human brain cDNAs.
Nature genetics 1992;2(3):180-5.
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1992: Xiao H; Merril C R; Polymeropoulos M H
Dinucleotide repeat polymorphisms at the D3S1246 and D3S1247 loci.
Human molecular genetics 1992;1(8):652.
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1992: Polymeropoulos M H; Xiao H; Merril C R
Tetranucleotide repeat polymorphism at the human myelin basic protein gene (MBP).
Human molecular genetics 1992;1(8):658.
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1992: Polymeropoulos M H; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the D9S147E locus.
Human molecular genetics 1992;1(7):549.
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1992: Xiao H; Merril C R; Polymeropoulos M H
Dinucleotide repeat polymorphism at the D7S476 locus.
Human molecular genetics 1992;1(7):549.
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1992: Polymeropoulos M H; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the D5S356 locus.
Human molecular genetics 1992;1(4):290.
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1992: Xiao H; Merril C R; Polymeropoulos M H
Dinucleotide repeat polymorphism at the D3S1229 locus.
Human molecular genetics 1992;1(4):290.
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1992: Bodenteich A; Mitchell L G; Polymeropoulos M H; Merril C R
Dinucleotide repeat in the human mitochondrial D-loop.
Human molecular genetics 1992;1(2):140.
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1992: Polymeropoulos M H; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the human c-myc oncogene locus (MYC).
Human molecular genetics 1992;1(1):65.
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1992: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Tetranucleotide repeat polymorphism at the human beta-actin related pseudogene H-beta-Ac-psi-2 (ACTBP2).
Nucleic acids research 1992;20(6):1432.
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1992: Polymeropoulos M H; Xiao H; Glodek A; Gorski M; Adams M D; Moreno R F; Fitzgerald M G; Venter J C; Merril C R
Chromosomal assignment of 46 brain cDNAs.
Genomics 1992;12(3):492-6.
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1991: Polymeropoulos M H; Xiao H; Merril C R
The human D5 dopamine receptor (DRD5) maps on chromosome 4.
Genomics 1991;11(3):777-8.
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1991: Weber J L; Polymeropoulos M H; May P E; Kwitek A E; Xiao H; McPherson J D; Wasmuth J J
Mapping of human chromosome 5 microsatellite DNA polymorphisms.
Genomics 1991;11(3):695-700.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the human beta 1 subunit of the GABAA receptor gene (GABRB1).
Nucleic acids research 1991;19(22):6345.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the human gene for insulin-like growth factor I (IGFI).
Nucleic acids research 1991;19(20):5797.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Tetranucleotide repeat polymorphism at the human prostatic acid phosphatase (ACPP) gene.
Nucleic acids research 1991;19(17):4792.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Tetranucleotide repeat polymorphism at the human dihydrofolate reductase psi-2 pseudogene (DHFRP2).
Nucleic acids research 1991;19(17):4792.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Trinucleotide repeat polymorphism at the human gamma-B-crystallin gene.
Nucleic acids research 1991;19(16):4571.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Trinucleotide repeat polymorphism at the human transcription factor IID gene.
Nucleic acids research 1991;19(15):4307.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Trinucleotide repeat polymorphism at the human met-tRNA-i gene 1 (TRMI).
Nucleic acids research 1991;19(15):4306.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Tetranucleotide repeat polymorphism at the human coagulation factor XIII A subunit gene (F13A1).
Nucleic acids research 1991;19(15):4306.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Dinucleotide repeat polymorphism at the human cardiac beta-myosin gene.
Nucleic acids research 1991;19(14):4019.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Tetranucleotide repeat polymorphism at the human c-fes/fps proto-oncogene (FES).
Nucleic acids research 1991;19(14):4018.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Dinucleotide repeat polymorphism at the human CTLA4 gene.
Nucleic acids research 1991;19(14):4018.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Dinucleotide repeat polymorphism at the human non-histone chromosomal protein HMG14 gene.
Nucleic acids research 1991;19(13):3753.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the human ATP synthase beta subunit gene (ATPSB).
Nucleic acids research 1991;19(14):4019.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH).
Nucleic acids research 1991;19(13):3753.
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1991: Adams M D; Kelley J M; Gocayne J D; Dubnick M; Polymeropoulos M H; Xiao H; Merril C R; Wu A; Olde B; Moreno R F
Complementary DNA sequencing: expressed sequence tags and human genome project.
Science (New York, N.Y.) 1991;252(5013):1651-6.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the human fms-related tyrosine kinase gene (FLT1).
Nucleic acids research 1991;19(10):2803.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the human liver-type 6-phosphofructokinase (PFKL) gene.
Nucleic acids research 1991;19(9):2517.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the human debrisoquine 4-hydroxylase (CYP2D) locus.
Nucleic acids research 1991;19(8):1961.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Dinucleotide repeat polymorphism at the human MHC class I CD8 alpha-chain (Leu-2/T8) gene.
Nucleic acids research 1991;19(7):1718.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Dinucleotide repeat polymorphism at the human gene of the light and heavy chains of myeloperoxidase glycoprotein (MPO).
Nucleic acids research 1991;19(8):1961.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Dinucleotide repeat polymorphism at the human cysteine-proteinase inhibitor pseudogene (CSTP1).
Nucleic acids research 1991;19(5):1164.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Dinucleotide repeat polymorphism at the human c-fms protooncogene for the CFS-1 receptor (CFS1R).
Nucleic acids research 1991;19(5):1160.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
A simple sequence repeat polymorphism at the human growth hormone locus.
Nucleic acids research 1991;19(3):689.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the human preproglucagon gene.
Nucleic acids research 1991;19(3):688.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Dinucleotide repeat polymorphism at the human interleukin 9 gene.
Nucleic acids research 1991;19(3):688.
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1991: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Dinucleotide repeat polymorphism at the human ankyrin gene (ANK1).
Nucleic acids research 1991;19(4):969.
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1991: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Tetranucleotide repeat polymorphism at the human aromatase cytochrome P-450 gene (CYP19).
Nucleic acids research 1991;19(1):195.
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1990: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Trinucleotide repeat polymorphism at the human intestinal fatty acid binding protein gene (FABP2).
Nucleic acids research 1990;18(23):7198.
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1990: Polymeropoulos M H; Rath D S; Xiao H; Merril C R
Trinucleotide repeat polymorphism at the human pancreatic phospholipase A-2 gene (PLA2).
Nucleic acids research 1990;18(24):7468.
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1990: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Dinucleotide repeat polymorphism at the int-2 proto-oncogene locus (INT2).
Nucleic acids research 1990;18(24):7468.
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1990: Polymeropoulos M H; Xiao H; Rath D S; Merril C R
Dinucleotide repeat polymorphism at the human thrombospondin gene (THBS1).
Nucleic acids research 1990;18(24):7467.
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1990: Weber J L; Kwitek A E; May P E; Polymeropoulos M
Dinucleotide repeat polymorphism at the D12S43 locus.
Nucleic acids research 1990;18(15):4637.
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1990: Weber J L; Kwitek A E; May P E; Polymeropoulos M H; Ledbetter S
Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci.
Nucleic acids research 1990;18(13):4037.
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