| Utilité clinique des genome boards pour les maladies génétiques complexes | Revue médicale suisse | | | 2023 | 203 | 216 |
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| Prise en charge des maladies rénales génétiques : expérience locale et importance du réseau | Revue médicale suisse | | | 2023 | 103 | 126 |
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| Epigenomic changes after acupuncture treatment in patients suffering from burnout | Complementary medicine research | | | 2022 | 343 | 10 |
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| GnRH replacement rescues cognition in Down syndrome | Science | | | 2022 | 325 | 1 |
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| 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 | 516 | 439 |
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| Increased Arterial Responsiveness to Angiotensin II in Mice Conceived by Assisted Reproductive Technologies | International journal of molecular sciences | | | 2022 | 328 | 236 |
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| Glomerulocystic kidney disease | Kidney international | | | 2022 | 87 | 0 |
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| Altered DNA methylation in estrogen-responsive repetitive sequences of spermatozoa of infertile men with shortened anogenital distance | Clinical epigenetics | | | 2022 | 239 | 354 |
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| Gestational trophoblastic disease in Switzerland: retrospective study of the impact of a regional reference centre | Swiss Medical Weekly | | | 2021 | 347 | 199 |
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| Epigenomic analyses in sub-populations of spermatozoa from infertile men with short anogenital distance | EUROTOX 2021 | | | 2021 | 279 | 270 |
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| Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients | Human Mutation | | | 2021 | 385 | 571 |
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| Benefits of exome sequencing in children with suspected isolated hearing loss | Genes | | | 2021 | 325 | 540 |
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| 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 | 262 | 295 |
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| Altered BDNF methylation in patients with chronic musculoskeletal pain and high biopsychosocial complexity | Journal of Pain Research | | | 2020 | 313 | 199 |
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| Case report: a 58 -year -old man with small kidneys and elevated liver enzymes | BMC Nephrology | | | 2020 | 395 | 230 |
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| Triméthylaminurie : un cas pas forcément si rare | Revue médicale suisse | | | 2020 | 405 | 709 |
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| LARS2-Perrault syndrome: a new case report and literature review | BMC Medical Genetics | | | 2020 | 488 | 612 |
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| Génétique des troubles auditifs chez l'enfant | Revue médicale suisse | | | 2019 | 410 | 389 |
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| Tests préimplantatoires de l'embryon en médecine de reproduction | Revue médicale suisse | | | 2019 | 375 | 164 |
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| Genetic resistance to DEHP-induced transgenerational endocrine disruption | PLOS ONE | | | 2019 | 556 | 374 |
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| Entre gènes et sexe : quelle détermination ? | Revue médicale suisse | | | 2019 | 454 | 680 |
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| Handicap intellectuel : apport de la génétique pour le diagnostic étiologique | Revue médicale suisse | | | 2018 | 477 | 162 |
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| Intergenerational Transmission of DNA Methylation Signatures Associated with Early Life Stress | Current Genomics | | | 2018 | 870 | 3 |
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| 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 | 565 | 314 |
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| 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 | 469 | 594 |
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| L'instinct aurait-il une base épigénétique ? | Revue médicale suisse | | | 2017 | 436 | 313 |
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| 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 | 738 | 341 |
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| The association of serotonin receptor 3A methylation with maternal violence exposure, neural activity, and child aggression | Behavioural brain research | | | 2017 | 769 | 409 |
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| Patients avec variation du développement sexuel : un exemple de prise en charge interdisciplinaire | Revue médicale suisse | | | 2016 | 342 | 410 |
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| Maladies génétiques rénales : perspectives diagnostiques | Revue médicale suisse | | | 2016 | 557 | 3 |
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| 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 | 930 | 9 |
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| Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders | Human genomics | | | 2016 | 755 | 364 |
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| BDNF promoter I methylation correlates between post-mortem human peripheral and brain tissues | Neuroscience research | | | 2015 | 859 | 1,449 |
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| BDNF Methylation and Maternal Brain Activity in a Violence-Related Sample | PloS one | | | 2015 | 798 | 472 |
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| Prenatal Exposure to DEHP Affects Spermatogenesis and Sperm DNA Methylation in a Strain-Dependent Manner | PloS one | | | 2015 | 777 | 639 |
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| 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 | 547 | 1 |
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| 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 | 844 | 719 |
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| The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axis | The world journal of biological psychiatry | | | 2014 | 1,280 | 8 |
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| Epigénétique et transmission | Revue médicale suisse | | | 2014 | 233 | 109 |
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| Epigenetic effects of methoxychlor and vinclozolin on male gametes | Vitamins and hormones | | | 2014 | 539 | 0 |
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| Mice generated by in vitro fertilization exhibit vascular dysfunction and shortened life span | The Journal of clinical investigation | | | 2013 | 649 | 386 |
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| Effect of developmental dioxin exposure on methylation and expression of specific imprinted genes in mice | Reproductive toxicology | | | 2013 | 608 | 5 |
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| Stochasticité : la troisième variable | Revue médicale suisse | | | 2013 | 592 | 2 |
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| Autisme, à chacun son génome | | | | 2012 | 716 | 441 |
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| La fin du dimorphisme sexuel est-elle programmée ? | Revue médicale suisse | | | 2011 | 597 | 0 |
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| Prenatal exposure to ethanol: a specific effect on the H19 gene in sperm | Reproductive toxicology | | | 2011 | 710 | 4 |
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| Post genomic decade - the epigenome and exposome challenges | Schweizerische medizinische Wochenschrift | | | 2011 | 576 | 2 |
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| De l'épigénome à l'exposome | Revue médicale suisse | | | 2011 | 580 | 6 |
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| 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 | 1,478 | 0 |
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| 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 | 632 | 0 |
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| Maladies trophoblastiques : une prise en charge pluridisciplinaire, un premier centre suisse | Revue médicale suisse | | | 2011 | 659 | 3 |
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| Specific transgenerational imprinting effects of the endocrine disruptor methoxychlor on male gametes | Reproduction | | | 2011 | 684 | 3 |
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| Mild intellectual disability associated with a progeny of father-daughter incest: genetic and environmental considerations | Journal of child sexual abuse | | | 2010 | 660 | 0 |
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| Transgenerational effects of the endocrine disruptor vinclozolin on the methylation pattern of imprinted genes in the mouse sperm | Reproduction | | | 2010 | 225 | 0 |
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| Epigenetic modulations in infertility and reproductive medicine | | | | 2010 | 696 | 15 |
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| 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 | 704 | 0 |
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| Superovulation in mice alters the methylation pattern of imprinted genes in the sperm of the offspring | Reproductive Toxicology | | | 2009 | 268 | 0 |
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| A reservoir of brown adipocyte progenitors in human skeletal muscle | Stem Cells | | | 2008 | 271 | 0 |
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| Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome | European Journal of Medical Genetics | | | 2008 | 209 | 0 |
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| Epigenetics in reproductive medicine | Pediatric Research | | | 2007 | 202 | 0 |
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| Chromosome Y polysomy: a non-mosaic 49,XYYYY case | Clinical Dysmorphology | | | 2007 | 285 | 0 |
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| Conserved features of imprinted differentially methylated domains | Gene | | | 2007 | 212 | 0 |
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| Genetic and epigenetic risks of ART | Fertility and Sterility | | | 2007 | 168 | 0 |
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| Evolutionary appearance of mononucleotide repeats in the coding sequences of four genes in primates | Journal of Genetics | | | 2007 | 188 | 0 |
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| Specific language impairment as the prominent feature in a patient with a low-level trisomy 21 mosaicism | Journal of Intellectual Disability Research | | | 2007 | 312 | 0 |
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| Implications of reproductive technologies for birth and developmental outcomes: imprinting defects and beyond | Expert Reviews in Molecular Medicine | | | 2006 | 161 | 0 |
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| Specific differentially methylated domain sequences direct the maintenance of methylation at imprinted genes | Molecular and Cellular Biology | | | 2006 | 184 | 0 |
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| Six cases of cryptic subtelomeric translocations in four families: the use of subtelomeric FISH probes as a diagnostic tool | Genetic Counseling | | | 2006 | 171 | 0 |
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| Preimplantation genetic diagnosis and epigenetics?- continued surveillance | Fertility and Sterility | | | 2006 | 191 | 0 |
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| The role of DMDs in the maintenance of epigenetic states | Cytogenetic and Genome Research | | | 2006 | 185 | 0 |
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| Epigenetic counseling | Genetic Counseling | | | 2006 | 150 | 0 |
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| Reproduction assistée: quelles incertitudes génétiques ? | Revue médicale suisse | | | 2005 | 133 | 41 |
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| Fille ou garçon: qui décide ? | Revue médicale suisse | | | 2005 | 171 | 42 |
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| Empreinte génomique, la bataille des sexes ? | Revue médicale suisse | | | 2005 | 191 | 57 |
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| Parenteral nutrition practices in hospital pharmacies in Switzerland, France, and Belgium | Nutrition | | | 2004 | 217 | 0 |
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| Genetics and nutrition | Clinical Nutrition | | | 2003 | 244 | 0 |
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| Pregnancy outcome of 30 fetuses with cystic hygroma diagnosed during the first 15 weeks of gestation | Genetic counseling | | | 2003 | 220 | 0 |
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| Hormone de croissance et carcinogenèse: le point sur la question | Revue médicale de la Suisse romande | | | 2003 | 718 | 0 |
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| Prise de conscience des problèmes nutritionnels dans les hôpitaux: quelles solutions ? | Revue médicale de la Suisse romande | | | 2003 | 178 | 69 |
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| Differential rates of frameshift alterations in four repeat sequences of hereditary nonpolyposis colorectal cancer tumors | Human genetics | | | 2002 | 600 | 1 |
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| Fire-settng behavior associated with Klinefelter syndrome | International Journal of Psychiatry in Medicine | | | 2002 | 177 | 0 |
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| Frequency of replication/transcription errors in (A)/(T) runs of human genes | Human genetics | | | 2001 | 570 | 0 |
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| A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonography | Gynecological endocrinology | | | 2000 | 622 | 0 |
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| 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 | 649 | 1 |
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| Cloning of the TMPRSS2 gene, which encodes a novel serine protease with transmembrane, LDLRA, and SRCR domains and maps to 21q22.3 | Genomics | | | 1997 | 667 | 0 |
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