AG
Giacobino, Ariane
| Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
|---|---|---|---|---|---|---|---|
| Utilité clinique des genome boards pour les maladies génétiques complexes | Revue médicale suisse |  | 2023 | 195 | 156 | ||
| Prise en charge des maladies rénales génétiques : expérience locale et importance du réseau | Revue médicale suisse | | 2023 | 96 | 103 | ||
| Epigenomic changes after acupuncture treatment in patients suffering from burnout | Complementary medicine research |  | 2022 | 332 | 10 | ||
| GnRH replacement rescues cognition in Down syndrome | Science | | 2022 | 319 | 1 | ||
| The relationship of maternal and child methylation of the glucocorticoid receptor NR3C1 during early childhood and subsequent child psychopathology at school-age in the context of maternal interpersonal violence-related post-traumatic stress disorder | Frontiers in psychiatry | | 2022 | 501 | 398 | ||
| Increased Arterial Responsiveness to Angiotensin II in Mice Conceived by Assisted Reproductive Technologies | International journal of molecular sciences | | 2022 | 322 | 176 | ||
| Glomerulocystic kidney disease | Kidney international | | 2022 | 81 | 0 | ||
| Altered DNA methylation in estrogen-responsive repetitive sequences of spermatozoa of infertile men with shortened anogenital distance | Clinical epigenetics | | 2022 | 233 | 257 | ||
| Gestational trophoblastic disease in Switzerland: retrospective study of the impact of a regional reference centre | Swiss Medical Weekly | | 2021 | 341 | 180 | ||
| Epigenomic analyses in sub-populations of spermatozoa from infertile men with short anogenital distance | EUROTOX 2021 | | 2021 | 273 | 243 | ||
| Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients | Human Mutation | | 2021 | 379 | 486 | ||
| Benefits of exome sequencing in children with suspected isolated hearing loss | Genes | | 2021 | 317 | 450 | ||
| Genome-wide epigenomic analyses in patients with nociceptive and neuropathic chronic pain subtypes reveals alterations in methylation of genes involved in the neuro-musculoskeletal system | Journal of Pain | | 2021 | 255 | 261 | ||
| Altered BDNF methylation in patients with chronic musculoskeletal pain and high biopsychosocial complexity | Journal of Pain Research | | 2020 | 307 | 190 | ||
| Case report: a 58 -year -old man with small kidneys and elevated liver enzymes | BMC Nephrology | | 2020 | 389 | 214 | ||
| Triméthylaminurie : un cas pas forcément si rare | Revue médicale suisse | | 2020 | 397 | 629 | ||
| LARS2-Perrault syndrome: a new case report and literature review | BMC Medical Genetics | | 2020 | 480 | 497 | ||
| Génétique des troubles auditifs chez l'enfant | Revue médicale suisse | | 2019 | 404 | 352 | ||
| Tests préimplantatoires de l'embryon en médecine de reproduction | Revue médicale suisse | | 2019 | 369 | 143 | ||
| Genetic resistance to DEHP-induced transgenerational endocrine disruption | PLOS ONE | | 2019 | 550 | 363 | ||
| Entre gènes et sexe : quelle détermination ? | Revue médicale suisse | | 2019 | 443 | 600 | ||
| Handicap intellectuel : apport de la génétique pour le diagnostic étiologique | Revue médicale suisse | | 2018 | 469 | 153 | ||
| Intergenerational Transmission of DNA Methylation Signatures Associated with Early Life Stress | Current Genomics | | 2018 | 858 | 3 | ||
| Recipient rs1045642 Polymorphism Is Associated With Office Blood Pressure at 1-Year Post Kidney Transplantation: A Single Center Pharmacogenetic Cohort Pilot Study | Frontiers in Pharmacology | | 2018 | 559 | 282 | ||
| Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother | Journal of Human Genetics | | 2018 | 461 | 543 | ||
| L'instinct aurait-il une base épigénétique ? | Revue médicale suisse | | 2017 | 429 | 286 | ||
| Testicular Dysgenesis Syndrome and Long-Lasting Epigenetic Silencing of Mouse Sperm Genes Involved in the Reproductive System after Prenatal Exposure to DEHP | PloS one | | 2017 | 729 | 333 | ||
| The association of serotonin receptor 3A methylation with maternal violence exposure, neural activity, and child aggression | Behavioural brain research | | 2017 | 758 | 384 | ||
| Patients avec variation du développement sexuel : un exemple de prise en charge interdisciplinaire | Revue médicale suisse | | 2016 | 336 | 377 | ||
| Maladies génétiques rénales : perspectives diagnostiques | Revue médicale suisse | | 2016 | 549 | 3 | ||
| Methylation of Serotonin Receptor 3a in ADHD, Borderline Personality, and Bipolar Disorders: Link with Severity of the Disorders and Childhood Maltreatment | Depression and anxiety | | 2016 | 922 | 9 | ||
| Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders | Human genomics | | 2016 | 747 | 327 | ||
| BDNF promoter I methylation correlates between post-mortem human peripheral and brain tissues | Neuroscience research | | 2015 | 851 | 1,377 | ||
| BDNF Methylation and Maternal Brain Activity in a Violence-Related Sample | PloS one | | 2015 | 788 | 464 | ||
| Prenatal Exposure to DEHP Affects Spermatogenesis and Sperm DNA Methylation in a Strain-Dependent Manner | PloS one | | 2015 | 765 | 618 | ||
| Prevention of vascular dysfunction and arterial hypertension in mice generated by assisted reproductive technologies by addition of melatonin to culture media | American journal of physiology. Heart and circulatory physiology | | 2015 | 539 | 1 | ||
| Methylation of NR3C1 is related to maternal PTSD, parenting stress and maternal medial prefrontal cortical activity in response to child separation among mothers with histories of violence exposure | Frontiers in psychology | | 2015 | 836 | 688 | ||
| The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axis | The world journal of biological psychiatry | | 2014 | 1,269 | 8 | ||
| Epigénétique et transmission | Revue médicale suisse | | 2014 | 225 | 91 | ||
| Epigenetic effects of methoxychlor and vinclozolin on male gametes | Vitamins and hormones | 2014 | 531 | 0 | |||
| Mice generated by in vitro fertilization exhibit vascular dysfunction and shortened life span | The Journal of clinical investigation | | 2013 | 641 | 357 | ||
| Effect of developmental dioxin exposure on methylation and expression of specific imprinted genes in mice | Reproductive toxicology | | 2013 | 600 | 5 | ||
| Stochasticité : la troisième variable | Revue médicale suisse | | 2013 | 584 | 2 | ||
| Autisme, à chacun son génome | 2012 | 708 | 441 | ||||
| La fin du dimorphisme sexuel est-elle programmée ? | Revue médicale suisse | | 2011 | 589 | 0 | ||
| Prenatal exposure to ethanol: a specific effect on the H19 gene in sperm | Reproductive toxicology | | 2011 | 702 | 4 | ||
| Post genomic decade - the epigenome and exposome challenges | Schweizerische medizinische Wochenschrift | | 2011 | 567 | 2 | ||
| De l'épigénome à l'exposome | Revue médicale suisse | | 2011 | 572 | 6 | ||
| Increased methylation of glucocorticoid receptor gene (NR3C1) in adults with a history of childhood maltreatment: a link with the severity and type of trauma | Translational psychiatry | | 2011 | 1,468 | 0 | ||
| Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing | Investigative ophthalmology & visual science | | 2011 | 623 | 0 | ||
| Maladies trophoblastiques : une prise en charge pluridisciplinaire, un premier centre suisse | Revue médicale suisse | | 2011 | 651 | 3 | ||
| Specific transgenerational imprinting effects of the endocrine disruptor methoxychlor on male gametes | Reproduction | | 2011 | 676 | 3 | ||
| Mild intellectual disability associated with a progeny of father-daughter incest: genetic and environmental considerations | Journal of child sexual abuse | | 2010 | 652 | 0 | ||
| Transgenerational effects of the endocrine disruptor vinclozolin on the methylation pattern of imprinted genes in the mouse sperm | Reproduction | | 2010 | 218 | 0 | ||
| Epigenetic modulations in infertility and reproductive medicine | | 2010 | 687 | 15 | |||
| Characterization of an interstitial deletion 6q13-q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms | European journal of medical genetics | | 2009 | 696 | 0 | ||
| Superovulation in mice alters the methylation pattern of imprinted genes in the sperm of the offspring | Reproductive Toxicology | | 2009 | 262 | 0 | ||
| A reservoir of brown adipocyte progenitors in human skeletal muscle | Stem Cells | | 2008 | 265 | 0 | ||
| Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome | European Journal of Medical Genetics | | 2008 | 203 | 0 | ||
| Epigenetics in reproductive medicine | Pediatric Research | | 2007 | 196 | 0 | ||
| Chromosome Y polysomy: a non-mosaic 49,XYYYY case | Clinical Dysmorphology | | 2007 | 279 | 0 | ||
| Conserved features of imprinted differentially methylated domains | Gene | | 2007 | 206 | 0 | ||
| Genetic and epigenetic risks of ART | Fertility and Sterility | | 2007 | 162 | 0 | ||
| Evolutionary appearance of mononucleotide repeats in the coding sequences of four genes in primates | Journal of Genetics | | 2007 | 182 | 0 | ||
| Specific language impairment as the prominent feature in a patient with a low-level trisomy 21 mosaicism | Journal of Intellectual Disability Research | | 2007 | 306 | 0 | ||
| Implications of reproductive technologies for birth and developmental outcomes: imprinting defects and beyond | Expert Reviews in Molecular Medicine | | 2006 | 155 | 0 | ||
| Specific differentially methylated domain sequences direct the maintenance of methylation at imprinted genes | Molecular and Cellular Biology | | 2006 | 178 | 0 | ||
| Six cases of cryptic subtelomeric translocations in four families: the use of subtelomeric FISH probes as a diagnostic tool | Genetic Counseling | | 2006 | 165 | 0 | ||
| Preimplantation genetic diagnosis and epigenetics?- continued surveillance | Fertility and Sterility | | 2006 | 184 | 0 | ||
| The role of DMDs in the maintenance of epigenetic states | Cytogenetic and Genome Research | | 2006 | 179 | 0 | ||
| Epigenetic counseling | Genetic Counseling | | 2006 | 144 | 0 | ||
| Reproduction assistée: quelles incertitudes génétiques ? | Revue médicale suisse | | 2005 | 127 | 28 | ||
| Fille ou garçon: qui décide ? | Revue médicale suisse | | 2005 | 165 | 36 | ||
| Empreinte génomique, la bataille des sexes ? | Revue médicale suisse | | 2005 | 185 | 48 | ||
| Parenteral nutrition practices in hospital pharmacies in Switzerland, France, and Belgium | Nutrition | | 2004 | 210 | 0 | ||
| Genetics and nutrition | Clinical Nutrition | | 2003 | 238 | 0 | ||
| Pregnancy outcome of 30 fetuses with cystic hygroma diagnosed during the first 15 weeks of gestation | Genetic counseling | | 2003 | 214 | 0 | ||
| Hormone de croissance et carcinogenèse: le point sur la question | Revue médicale de la Suisse romande | | 2003 | 710 | 0 | ||
| Prise de conscience des problèmes nutritionnels dans les hôpitaux: quelles solutions ? | Revue médicale de la Suisse romande | | 2003 | 172 | 55 | ||
| Differential rates of frameshift alterations in four repeat sequences of hereditary nonpolyposis colorectal cancer tumors | Human genetics | | 2002 | 592 | 1 | ||
| Fire-settng behavior associated with Klinefelter syndrome | International Journal of Psychiatry in Medicine | | 2002 | 169 | 0 | ||
| Frequency of replication/transcription errors in (A)/(T) runs of human genes | Human genetics | | 2001 | 560 | 0 | ||
| A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonography | Gynecological endocrinology | | 2000 | 614 | 0 | ||
| Cloning of a novel human neural cell adhesion molecule gene (NCAM2) that maps to chromosome region 21q21 and is potentially involved in Down syndrome | Genomics | | 1997 | 641 | 1 | ||
| Cloning of the TMPRSS2 gene, which encodes a novel serine protease with transmembrane, LDLRA, and SRCR domains and maps to 21q22.3 | Genomics | | 1997 | 659 | 0 |
