Giacobino, Ariane

 
Title Year Hits Downloads
Increased methylation of glucocorticoid receptor gene (NR3C1) in adults with a history of childhood maltreatment: a link with the severity and type of trauma 2011 1005 0
The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axis 2014 606 7
BDNF promoter I methylation correlates between post-mortem human peripheral and brain tissues 2015 518 838
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 2015 503 335
Methylation of Serotonin Receptor 3a in ADHD, Borderline Personality, and Bipolar Disorders: Link with Severity of the Disorders and Childhood Maltreatment 2016 492 8
Prenatal Exposure to DEHP Affects Spermatogenesis and Sperm DNA Methylation in a Strain-Dependent Manner 2015 470 387
Specific transgenerational imprinting effects of the endocrine disruptor methoxychlor on male gametes 2011 440 3
Mild intellectual disability associated with a progeny of father-daughter incest: genetic and environmental considerations 2010 437 0
BDNF Methylation and Maternal Brain Activity in a Violence-Related Sample 2015 434 195
Prenatal exposure to ethanol: a specific effect on the H19 gene in sperm 2011 430 3
Cloning of the TMPRSS2 gene, which encodes a novel serine protease with transmembrane, LDLRA, and SRCR domains and maps to 21q22.3 1997 427 0
Autisme, à chacun son génome 2012 426 188
Characterization of an interstitial deletion 6q13-q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms 2009 424 0
Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders 2016 424 138
Epigenetic modulations in infertility and reproductive medicine 2010 419 13
Cloning of a novel human neural cell adhesion molecule gene (NCAM2) that maps to chromosome region 21q21 and is potentially involved in Down syndrome 1997 410 0
Intergenerational Transmission of DNA Methylation Signatures Associated with Early Life Stress 2018 410 1
The association of serotonin receptor 3A methylation with maternal violence exposure, neural activity, and child aggression 2017 406 85
De l’épigénome à l’exposome 2011 402 6
Testicular Dysgenesis Syndrome and Long-Lasting Epigenetic Silencing of Mouse Sperm Genes Involved in the Reproductive System after Prenatal Exposure to DEHP. 2017 397 179
Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing 2011 395 0
La fin du dimorphisme sexuel est-elle programmée ? 2011 395 0
A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonography 2000 375 0
Effect of developmental dioxin exposure on methylation and expression of specific imprinted genes in mice 2013 374 5
Stochasticité : la troisième variable 2013 370 2
Maladies trophoblastiques : une prise en charge pluridisciplinaire, un premier centre suisse 2011 366 2
Differential rates of frameshift alterations in four repeat sequences of hereditary nonpolyposis colorectal cancer tumors 2002 362 1
Mice generated by in vitro fertilization exhibit vascular dysfunction and shortened life span 2013 362 211
Post genomic decade - the epigenome and exposome challenges 2011 358 2
Frequency of replication/transcription errors in (A)/(T) runs of human genes 2001 330 0
Epigenetic effects of methoxychlor and vinclozolin on male gametes 2014 317 0
Prevention of vascular dysfunction and arterial hypertension in mice generated by assisted reproductive technologies by addition of melatonin to culture media 2015 301 1
Maladies génétiques rénales : perspectives diagnostiques 2016 297 3
Hormone de croissance et carcinogenèse: le point sur la question 2003 288 0
Recipient rs1045642 Polymorphism Is Associated With Office Blood Pressure at 1-Year Post Kidney Transplantation: A Single Center Pharmacogenetic Cohort Pilot Study 2018 268 101
Genetic resistance to DEHP-induced transgenerational endocrine disruption 2019 210 120
L’instinct aurait-il une base épigénétique ? 2017 154 49
Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother 2018 148 42
Handicap intellectuel : apport de la génétique pour le diagnostic étiologique 2018 102 29
Génétique des troubles auditifs chez l’enfant 2019 51 17
Entre gènes et sexe : quelle détermination ? 2019 49 6
Case report: a 58 -year -old man with small kidneys and elevated liver enzymes 2020 47 13
LARS2-Perrault syndrome: a new case report and literature review 2020 46 13
Tests préimplantatoires de l’embryon en médecine de reproduction 2019 45 12
Triméthylaminurie : un cas pas forcément si rare 2020 43 0
Altered BDNF methylation in patients with chronic musculoskeletal pain and high biopsychosocial complexity 2020 27 10
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