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Contributor Giacobino, Ariane

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Publications

85

Views

39,304

Downloads

14,451

Supervised works

0

Breakdown by access level

Textual representation
Access level
Public access 36
Restricted access 47
No fulltext 2

Distribution by access level (last 10 years)

Textual representation
Access level Public access Restricted access Closed access No fulltext
2017 3
2018 3 1
2019 4
2020 4
2021 5
2022 3 3
2023 2
2024
2025
2026

Distribution according to UNIGE OA policy

Textual representation
Open access policy Open Access Still embargoed Not Open Access
33 40

List of publications by Giacobino, Ariane

1 - 85 of 85
Title Published in Access level OA Policy Year Views Downloads
Utilité clinique des genome boards pour les maladies génétiques complexesRevue médicale suisse
 2023 205 231
Prise en charge des maladies rénales génétiques : expérience locale et importance du réseauRevue médicale suisse
 2023 104 133
Epigenomic changes after acupuncture treatment in patients suffering from burnoutComplementary medicine research
 2022 344 10
GnRH replacement rescues cognition in Down syndromeScience
 2022 326 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 disorderFrontiers in psychiatry
 2022 517 458
Increased Arterial Responsiveness to Angiotensin II in Mice Conceived by Assisted Reproductive TechnologiesInternational journal of molecular sciences
 2022 330 241
Glomerulocystic kidney diseaseKidney international
 2022 89 0
Altered DNA methylation in estrogen-responsive repetitive sequences of spermatozoa of infertile men with shortened anogenital distanceClinical epigenetics
 2022 241 362
Gestational trophoblastic disease in Switzerland: retrospective study of the impact of a regional reference centreSwiss Medical Weekly
 2021 348 237
Epigenomic analyses in sub-populations of spermatozoa from infertile men with short anogenital distanceEUROTOX 2021
 2021 280 280
Molecular characterization of pathogenic OTOA gene conversions in hearing loss patientsHuman Mutation
 2021 386 600
Benefits of exome sequencing in children with suspected isolated hearing lossGenes
 2021 326 556
Genome-wide epigenomic analyses in patients with nociceptive and neuropathic chronic pain subtypes reveals alterations in methylation of genes involved in the neuro-musculoskeletal systemJournal of Pain
 2021 263 323
Altered BDNF methylation in patients with chronic musculoskeletal pain and high biopsychosocial complexityJournal of Pain Research
 2020 314 205
Case report: a 58 -year -old man with small kidneys and elevated liver enzymesBMC Nephrology
 2020 396 240
Triméthylaminurie : un cas pas forcément si rareRevue médicale suisse
 2020 406 728
LARS2-Perrault syndrome: a new case report and literature reviewBMC Medical Genetics
 2020 489 642
Génétique des troubles auditifs chez l'enfantRevue médicale suisse
 2019 411 401
Tests préimplantatoires de l'embryon en médecine de reproductionRevue médicale suisse
 2019 377 171
Genetic resistance to DEHP-induced transgenerational endocrine disruptionPLOS ONE
 2019 558 380
Entre gènes et sexe : quelle détermination ?Revue médicale suisse
 2019 455 696
Handicap intellectuel : apport de la génétique pour le diagnostic étiologiqueRevue médicale suisse
 2018 478 167
Intergenerational Transmission of DNA Methylation Signatures Associated with Early Life StressCurrent Genomics
 2018 871 3
Recipient rs1045642 Polymorphism Is Associated With Office Blood Pressure at 1-Year Post Kidney Transplantation: A Single Center Pharmacogenetic Cohort Pilot StudyFrontiers in Pharmacology
 2018 566 322
Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected motherJournal of Human Genetics
 2018 470 611
L'instinct aurait-il une base épigénétique ?Revue médicale suisse
 2017 437 321
Testicular Dysgenesis Syndrome and Long-Lasting Epigenetic Silencing of Mouse Sperm Genes Involved in the Reproductive System after Prenatal Exposure to DEHPPloS one
 2017 739 348
The association of serotonin receptor 3A methylation with maternal violence exposure, neural activity, and child aggressionBehavioural brain research
 2017 770 420
Patients avec variation du développement sexuel : un exemple de prise en charge interdisciplinaireRevue médicale suisse
 2016 343 422
Maladies génétiques rénales : perspectives diagnostiquesRevue médicale suisse
 2016 558 3
Methylation of Serotonin Receptor 3a in ADHD, Borderline Personality, and Bipolar Disorders: Link with Severity of the Disorders and Childhood MaltreatmentDepression and anxiety
 2016 931 9
Experience of a multidisciplinary task force with exome sequencing for Mendelian disordersHuman genomics
 2016 756 371
BDNF promoter I methylation correlates between post-mortem human peripheral and brain tissuesNeuroscience research
 2015 860 1,467
BDNF Methylation and Maternal Brain Activity in a Violence-Related SamplePloS one
 2015 799 482
Prenatal Exposure to DEHP Affects Spermatogenesis and Sperm DNA Methylation in a Strain-Dependent MannerPloS one
 2015 778 644
Prevention of vascular dysfunction and arterial hypertension in mice generated by assisted reproductive technologies by addition of melatonin to culture mediaAmerican journal of physiology. Heart and circulatory physiology
 2015 548 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 exposureFrontiers in psychology
 2015 845 726
The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axisThe world journal of biological psychiatry
 2014 1,281 8
Epigénétique et transmissionRevue médicale suisse
 2014 234 113
Epigenetic effects of methoxychlor and vinclozolin on male gametesVitamins and hormones
 2014 549 0
Mice generated by in vitro fertilization exhibit vascular dysfunction and shortened life spanThe Journal of clinical investigation
 2013 650 392
Effect of developmental dioxin exposure on methylation and expression of specific imprinted genes in miceReproductive toxicology
 2013 609 5
Stochasticité : la troisième variableRevue médicale suisse
 2013 593 2
Autisme, à chacun son génome
 2012 718 441
La fin du dimorphisme sexuel est-elle programmée ?Revue médicale suisse
 2011 598 0
Prenatal exposure to ethanol: a specific effect on the H19 gene in spermReproductive toxicology
 2011 711 4
Post genomic decade - the epigenome and exposome challengesSchweizerische medizinische Wochenschrift
 2011 577 2
De l'épigénome à l'exposomeRevue médicale suisse
 2011 581 6
Increased methylation of glucocorticoid receptor gene (NR3C1) in adults with a history of childhood maltreatment: a link with the severity and type of traumaTranslational psychiatry
 2011 1,479 0
Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencingInvestigative ophthalmology & visual science
 2011 633 0
Maladies trophoblastiques : une prise en charge pluridisciplinaire, un premier centre suisseRevue médicale suisse
 2011 660 3
Specific transgenerational imprinting effects of the endocrine disruptor methoxychlor on male gametesReproduction
 2011 685 3
Mild intellectual disability associated with a progeny of father-daughter incest: genetic and environmental considerationsJournal of child sexual abuse
 2010 661 0
Transgenerational effects of the endocrine disruptor vinclozolin on the methylation pattern of imprinted genes in the mouse spermReproduction
 2010 226 0
Epigenetic modulations in infertility and reproductive medicine
 2010 697 15
Characterization of an interstitial deletion 6q13-q14.1 in a female with mild mental retardation, language delay and minor dysmorphismsEuropean journal of medical genetics
 2009 705 0
Superovulation in mice alters the methylation pattern of imprinted genes in the sperm of the offspringReproductive Toxicology
 2009 269 0
A reservoir of brown adipocyte progenitors in human skeletal muscleStem Cells
 2008 272 0
Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndromeEuropean Journal of Medical Genetics
 2008 210 0
Epigenetics in reproductive medicinePediatric Research
 2007 203 0
Chromosome Y polysomy: a non-mosaic 49,XYYYY caseClinical Dysmorphology
 2007 286 0
Conserved features of imprinted differentially methylated domainsGene
 2007 213 0
Genetic and epigenetic risks of ARTFertility and Sterility
 2007 169 0
Evolutionary appearance of mononucleotide repeats in the coding sequences of four genes in primatesJournal of Genetics
 2007 189 0
Specific language impairment as the prominent feature in a patient with a low-level trisomy 21 mosaicismJournal of Intellectual Disability Research
 2007 313 0
Implications of reproductive technologies for birth and developmental outcomes: imprinting defects and beyondExpert Reviews in Molecular Medicine
 2006 162 0
Specific differentially methylated domain sequences direct the maintenance of methylation at imprinted genesMolecular and Cellular Biology
 2006 185 0
Six cases of cryptic subtelomeric translocations in four families: the use of subtelomeric FISH probes as a diagnostic toolGenetic Counseling
 2006 172 0
Preimplantation genetic diagnosis and epigenetics?- continued surveillanceFertility and Sterility
 2006 192 0
The role of DMDs in the maintenance of epigenetic statesCytogenetic and Genome Research
 2006 186 0
Epigenetic counselingGenetic Counseling
 2006 151 0
Reproduction assistée: quelles incertitudes génétiques ?Revue médicale suisse
 2005 134 46
Fille ou garçon: qui décide ?Revue médicale suisse
 2005 172 46
Empreinte génomique, la bataille des sexes ?Revue médicale suisse
 2005 192 71
Parenteral nutrition practices in hospital pharmacies in Switzerland, France, and BelgiumNutrition
 2004 218 0
Genetics and nutritionClinical Nutrition
 2003 245 0
Pregnancy outcome of 30 fetuses with cystic hygroma diagnosed during the first 15 weeks of gestationGenetic counseling
 2003 221 0
Hormone de croissance et carcinogenèse: le point sur la questionRevue médicale de la Suisse romande
 2003 719 0
Prise de conscience des problèmes nutritionnels dans les hôpitaux: quelles solutions ?Revue médicale de la Suisse romande
 2003 179 80
Differential rates of frameshift alterations in four repeat sequences of hereditary nonpolyposis colorectal cancer tumorsHuman genetics
 2002 601 1
Fire-settng behavior associated with Klinefelter syndromeInternational Journal of Psychiatry in Medicine
 2002 178 0
Frequency of replication/transcription errors in (A)/(T) runs of human genesHuman genetics
 2001 571 0
A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonographyGynecological endocrinology
 2000 623 0
Cloning of a novel human neural cell adhesion molecule gene (NCAM2) that maps to chromosome region 21q21 and is potentially involved in Down syndromeGenomics
 1997 650 1
Cloning of the TMPRSS2 gene, which encodes a novel serine protease with transmembrane, LDLRA, and SRCR domains and maps to 21q22.3Genomics
 1997 668 0
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