-X Estivill Researcher Activity Profile

Research Author Detailed Information 

X Estivill Publication Rate By Year

X Estivill has published 1 paper(s) in 2003, 2 paper(s) in 2005, 20 paper(s) in 2007, 14 paper(s) in 2008, for a total of 37 research publications in total.

X X Estivill Author Information

LAST NAME: estivill

FIRST NAME: X

INITIALS: x

AFFILIATION:

Papers

X Estivill's Publication Record

1. [Large-scale genotyping in research into autism spectrum disorders and attention deficit hyperactivity disorder.] Year Published: 2005
Centre de Regulacio Genomica (CRG), Barcelona, Espana.
2. Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles. Year Published: 2007
3. Altered brain-derived neurotrophic factor blood levels and gene variability are associated with anorexia and bulimia. Year Published: 2007
Genes and Disease Program, Center for Genomic Regulation, Barcelona Biomedical Research Park, Barcelona, Catalonia, Spain.
4. Differential responses to anxiogenic drugs in a mouse model of panic disorder as revealed by Fos immunocytochemistry in specific areas of the fear circuitry. Year Published: 2007
Genes and Disease Program, Center for Genomic Regulation (CRG), Barcelona Biomedical Research Park (PRBB), Barcelona, Spain.
5. Altered brain-derived neurotrophic factor blood levels and gene variability are associated with anorexia and bulimia. Year Published: 2007
Genes and Disease Program, Center for Genomic Regulation, Barcelona Biomedical Research Park, Barcelona, Catalonia, Spain.
6. Differential responses to anxiogenic drugs in a mouse model of panic disorder as revealed by Fos immunocytochemistry in specific areas of the fear circuitry. Year Published: 2007
Genes and Disease Program, Center for Genomic Regulation (CRG), Barcelona Biomedical Research Park (PRBB), Barcelona, Spain.
7. Altered brain-derived neurotrophic factor blood levels and gene variability are associated with anorexia and bulimia. Year Published: 2007
Genes and Disease Program, Center for Genomic Regulation, Barcelona Biomedical Research Park, Barcelona, Catalonia, Spain.
8. X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation. Year Published: 2008
Biochemistry and Molecular Genetics Department, Hospital Clínic and IDIBAPS (Institut d'Investigacions Biomèdiques August Pi i Sunyer), Barcelona, Spain. imadriba@gmail.com
9. Differential responses to anxiogenic drugs in a mouse model of panic disorder as revealed by Fos immunocytochemistry in specific areas of the fear circuitry. Year Published: 2007
Genes and Disease Program, Center for Genomic Regulation (CRG), Barcelona Biomedical Research Park (PRBB), Barcelona, Spain.
10. X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation. Year Published: 2008
11. Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations. Year Published: 2008
Dr M Witsch-Baumgartner, Department of Medical Genetics, Molecular and Clinical Pharmacology, Medical University Innsbruck, Schoepfstrasse 41, 6020 Innsbruck, Austria; Witsch-Baumgartner@i-med.ac.at.
12. Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations. Year Published: 2008
Department of Medical Genetics, Molecular and Clinical Pharmacology, Medical University Innsbruck, Schoepfstrasse 41, 6020 Innsbruck, Austria. Witsch-Baumgartner@i-med.ac.at
13. Expression profiles of the connexin genes, Gjb1 and Gjb3, in the developing mouse cochlea. Year Published: 2003
14. Different mechanisms preclude mutant CLDN14 proteins from forming tight junctions in vitro. Year Published: 2005
Department of Genetic Medicine and Development, University of Geneva Medical School and Geneva University Hospitals, Geneva, Switzerland.
15. Renaming the DSCR1/Adapt78 gene family as RCAN: regulators of calcineurin. Year Published: 2007
Ethel Percy Andrus Gerontology Center, and Division of Molecular & Computational Biology, The University of Southern California, Los Angeles, CA 90089-0191, USA. kelvin@usc.edu
16. Characterization and evolution of the novel gene family FAM90A in primates originated by multiple duplication and rearrangement events. Year Published: 2007
Genes and Disease Program, Center for Genomic Regulation (CRG-UPF) and CIBERESP, Barcelona, Catalonia, Spain.
17. Contribution of the serotoninergic system to anxious and depressive traits that may be partially responsible for the phenotypical variability of bulimia nervosa. Year Published: 2007
Genes and Disease Program, Center for Genomic Regulation, Barcelona Biomedical Research Park, Barcelona, Catalonia, Spain.
18. Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies. Year Published: 2007
Center for Genomic Regulation (CRG), National Genotyping Center (CeGen), CIBERESP, Pompeu Fabra University (UPF), Barcelona, Catalonia, Spain. xavier.estivill@crg.es
19. Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies. Year Published: 2007
Center for Genomic Regulation (CRG), National Genotyping Center (CeGen), CIBERESP, Pompeu Fabra University (UPF), Barcelona, Catalonia, Spain. xavier.estivill@crg.es
20. Characterization and evolution of the novel gene family FAM90A in primates originated by multiple duplication and rearrangement events. Year Published: 2007
Genes and Disease Program, Center for Genomic Regulation (CRG-UPF) and CIBERESP, Barcelona, Catalonia, Spain.
21. An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss. Year Published: 2007
Division of Molecular Medicine, The Walter and Eliza Hall Institute of Medical Research, Victoria, Australia.
22. Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies. Year Published: 2007
Center for Genomic Regulation (CRG), National Genotyping Center (CeGen), CIBERESP, Pompeu Fabra University (UPF), Barcelona, Catalonia, Spain. xavier.estivill@crg.es
23. An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss. Year Published: 2007
Division of Molecular Medicine, The Walter and Eliza Hall Institute of Medical Research, Victoria, Australia.
24. Renaming the DSCR1/Adapt78 gene family as RCAN: regulators of calcineurin. Year Published: 2007
Ethel Percy Andrus Gerontology Center, and Division of Molecular & Computational Biology, The University of Southern California, Los Angeles, CA 90089-0191, USA. kelvin@usc.edu
25. Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations. Year Published: 2008
Genetic Causes of Disease Group, Genes and Disease Program, Centre for Genomic Regulation (CRG), Barcelona, Catalonia, Spain.
26. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Year Published: 2007
27. Contribution of the serotoninergic system to anxious and depressive traits that may be partially responsible for the phenotypical variability of bulimia nervosa. Year Published: 2007
Genes and Disease Program, Center for Genomic Regulation, Barcelona Biomedical Research Park, Barcelona, Catalonia, Spain.
28. An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss. Year Published: 2007
Division of Molecular Medicine, The Walter and Eliza Hall Institute of Medical Research, Victoria, Australia.
29. Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations. Year Published: 2008
Genetic Causes of Disease Group, Genes and Disease Program, Centre for Genomic Regulation (CRG), Barcelona, Catalonia, Spain.
30. MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene. Year Published: 2008
Genes and Disease Program, Centre for Genomic Regulation (CRG), Barcelona, Catalonia, Spain. ester.ballana@gmail.com
31. MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene. Year Published: 2008
Genes and Disease Program, Centre for Genomic Regulation (CRG), Barcelona, Catalonia, Spain. ester.ballana@gmail.com
32. Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility. Year Published: 2008
Bioinformatics and Biostatistics Unit, and Translational Research Laboratory, Catalan Institute of Oncology, IDIBELL, L'Hospitalet, Barcelona, Spain. v.moreno@iconcologia.net.
33. Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility. Year Published: 2008
Bioinformatics and Biostatistics Unit, and Translational Research Laboratory, Catalan Institute of Oncology, IDIBELL, L'Hospitalet, Barcelona, Spain. x.sole@iconcologia.net
34. Developmental analysis of Lingo-1/Lern1 protein expression in the mouse brain: Interaction of its intracellular domain with Myt1l. Year Published: 2008
Bioinformatics and Genomics Program, Center for Genomic Regulation (CRG), UPF, Barcelona 08003, Spain.
35. Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia. Year Published: 2008
36. Maximizing association statistics over genetic models. Year Published: 2008
Center for Research in Environmental Epidemiology (CREAL), Barcelona, Spain.
37. Developmental analysis of Lingo-1/Lern1 protein expression in the mouse brain: interaction of its intracellular domain with Myt1l. Year Published: 2008
Bioinformatics and Genomics Program, Center for Genomic Regulation (CRG), UPF, Barcelona 08003, Spain.