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- [1] Biallelic TRAPPC10 variants are associated with a microcephalic TRAPPopathy disorder in humans and miceEUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 63 - 63Rawlins, Lettie Eleanor论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter, Exeter, Devon, England Univ Exeter, Exeter, Devon, EnglandAlmousa, Hashem论文数: 0 引用数: 0 h-index: 0机构: Concordia Univ, Montreal, PQ, Canada Univ Exeter, Exeter, Devon, EnglandKhan, Shazia论文数: 0 引用数: 0 h-index: 0机构: Int Islamic Univ, Islamabad, Pakistan Univ Exeter, Exeter, Devon, EnglandCollins, Stephan C.论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Dijon, France Univ Exeter, Exeter, Devon, EnglandMilev, Miroslav P.论文数: 0 引用数: 0 h-index: 0机构: Concordia Univ, Montreal, PQ, Canada Univ Exeter, Exeter, Devon, EnglandLeslie, Joseph S.论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter, Exeter, Devon, England Univ Exeter, Exeter, Devon, EnglandSaint-Dic, Djenann论文数: 0 引用数: 0 h-index: 0机构: Concordia Univ, Montreal, PQ, Canada Univ Exeter, Exeter, Devon, EnglandHincapie, Ana Maria论文数: 0 引用数: 0 h-index: 0机构: Concordia Univ, Montreal, PQ, Canada Univ Exeter, Exeter, Devon, EnglandHarlalka, Gaurav V.论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter, Exeter, Devon, England Univ Exeter, Exeter, Devon, EnglandVancollie, Valerie E.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Cambridge, England Univ Exeter, Exeter, Devon, EnglandLelliott, Christopher J.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Cambridge, England Univ Exeter, Exeter, Devon, England论文数: 引用数: h-index:机构:Yalcin, Binnaz论文数: 0 引用数: 0 h-index: 0机构: Univ Bourgogne Franche Comte, Dijon, France Univ Exeter, Exeter, Devon, EnglandCrosby, Andrew H.论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter, Exeter, Devon, England Univ Exeter, Exeter, Devon, England论文数: 引用数: h-index:机构:Baple, Emma L.论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter, Exeter, Devon, England Univ Exeter, Exeter, Devon, England
- [2] Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and micePLOS GENETICS, 2022, 18 (03):Rawlins, Lettie E.论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England Royal Devon & Exeter Hosp Heavitree, Peninsula Clin Genet Serv, Exeter, Devon, England Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England论文数: 引用数: h-index:机构:Khan, Shazia论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England Int Islamic Univ, Dept Biol Sci, Islamabad, Pakistan Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandCollins, Stephan C.论文数: 0 引用数: 0 h-index: 0机构: Inst Genet & Mol & Cellular Biol, Inserm, Illkirch Graffenstaden, France Univ Bourgogne Franche Comte, Inserm, Dijon, France Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandMilev, Miroslav P.论文数: 0 引用数: 0 h-index: 0机构: Concordia Univ, Dept Biol, Montreal, PQ, Canada Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England论文数: 引用数: h-index:机构:Saint-Dic, Djenann论文数: 0 引用数: 0 h-index: 0机构: Concordia Univ, Dept Biol, Montreal, PQ, Canada Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandKhan, Valeed论文数: 0 引用数: 0 h-index: 0机构: Rehman Med Inst, Dept Mol Diagnost, Peshawar, Pakistan Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandHincapie, Ana Maria论文数: 0 引用数: 0 h-index: 0机构: Concordia Univ, Dept Biol, Montreal, PQ, Canada Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandDay, Jacob O.论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England Univ Plymouth, Fac Hlth, Plymouth, England Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandMcGavin, Lucy论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Plymouth NHS Trust, Plymouth, England Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandRowley, Christine论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Cambridge, England Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandHarlalka, Gaurav V.论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England Rajarshi Shahu Coll Pharm, Dept Pharmacol, Buldana, India Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandVancollie, Valerie E.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Cambridge, England Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England论文数: 引用数: h-index:机构:Lelliott, Christopher J.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Cambridge, England Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England论文数: 引用数: h-index:机构:Yalcin, Binnaz论文数: 0 引用数: 0 h-index: 0机构: Inst Genet & Mol & Cellular Biol, Inserm, Illkirch Graffenstaden, France Univ Bourgogne Franche Comte, Inserm, Dijon, France Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandCrosby, Andrew H.论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandSacher, Michael论文数: 0 引用数: 0 h-index: 0机构: Concordia Univ, Dept Biol, Montreal, PQ, Canada McGill Univ, Dept Anat & Cell Biol, Montreal, PQ, Canada Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, EnglandBaple, Emma L.论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England Royal Devon & Exeter Hosp Heavitree, Peninsula Clin Genet Serv, Exeter, Devon, England Univ Exeter Med Sch, RD&E Wonford NHS Fdn Trust, RILD Wellcome Wolfson Med Res Ctr, Exeter, Devon, England
- [3] Insights on the Shared Genetic Landscape of Neurodevelopmental and Movement DisordersCURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2025, 25 (01)论文数: 引用数: h-index:机构:Zech, Michael论文数: 0 引用数: 0 h-index: 0机构: Helmholtz Munich, Inst Neurogen, Neuherberg, Germany Tech Univ Munich, Inst Human Genet, Sch Med, Munich, Germany Tech Univ Munich, Inst Adv Study, Garching, Germany Med Univ Innsbruck, Ctr Rare Movement Disorders Innsbruck, Dept Neurol, Anichstr 35, A-6020 Innsbruck, AustriaEberl, Anna论文数: 0 引用数: 0 h-index: 0机构: Med Univ Innsbruck, Ctr Rare Movement Disorders Innsbruck, Dept Neurol, Anichstr 35, A-6020 Innsbruck, Austria Med Univ Innsbruck, Ctr Rare Movement Disorders Innsbruck, Dept Neurol, Anichstr 35, A-6020 Innsbruck, AustriaBoesch, Sylvia论文数: 0 引用数: 0 h-index: 0机构: Med Univ Innsbruck, Ctr Rare Movement Disorders Innsbruck, Dept Neurol, Anichstr 35, A-6020 Innsbruck, Austria Med Univ Innsbruck, Ctr Rare Movement Disorders Innsbruck, Dept Neurol, Anichstr 35, A-6020 Innsbruck, Austria
- [4] Description of neurodevelopmental phenotypes associated with 10 genetic neurodevelopmental disorders: A scoping reviewCLINICAL GENETICS, 2021, 99 (03) : 335 - 346论文数: 引用数: h-index:机构:Shah, Harshil论文数: 0 引用数: 0 h-index: 0机构: Univ Calgary, Cumming Sch Med, Calgary, AB, Canada Univ Calgary, Cumming Sch Med, Calgary, AB, CanadaAu, Ping Yee Billie论文数: 0 引用数: 0 h-index: 0机构: Univ Calgary, Cumming Sch Med, Calgary, AB, Canada Univ Calgary, Dept Med Genet, Calgary, AB, Canada Univ Calgary, Alberta Childrens Hosp Res Inst, Calgary, AB, Canada Univ Calgary, Cumming Sch Med, Calgary, AB, CanadaMurias, Kara论文数: 0 引用数: 0 h-index: 0机构: Univ Calgary, Cumming Sch Med, Calgary, AB, Canada Univ Calgary, Dept Pediat, Calgary, AB, Canada Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada Univ Calgary, Alberta Childrens Hosp Res Inst, Calgary, AB, Canada Univ Calgary, Hotchkiss Brain Inst, Calgary, AB, Canada Univ Calgary, Cumming Sch Med, Calgary, AB, Canada
- [5] GENETIC VARIANTS UNDERLYING CHILDHOOD NEURODEVELOPMENTAL DISORDERS IN A DETAILED FINNISH COHORTEUROPEAN NEUROPSYCHOPHARMACOLOGY, 2024, 87 : 238 - 239Doagu, Fatma论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Neurosci Ctr, Helsinki, Finland Univ Helsinki, Neurosci Ctr, Helsinki, FinlandAlonso-Ortega, Alfredo论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Neurosci Ctr, Helsinki, Finland Univ Helsinki, Neurosci Ctr, Helsinki, FinlandOksanen-Hennah, Henna论文数: 0 引用数: 0 h-index: 0机构: Helsinki Univ Hosp, Pediat Neuropsychiat Unit, Helsinki, Finland Univ Helsinki, Neurosci Ctr, Helsinki, FinlandVanhala, Raija论文数: 0 引用数: 0 h-index: 0机构: Helsinki Univ Hosp, Pediat Neuropsychiat Unit, Helsinki, Finland Univ Helsinki, Neurosci Ctr, Helsinki, Finland论文数: 引用数: h-index:机构:Voutilainen, Arja论文数: 0 引用数: 0 h-index: 0机构: Helsinki Univ Hosp, Pediat Neuropsychiat Unit, Helsinki, Finland Univ Helsinki, Neurosci Ctr, Helsinki, FinlandTimonen-Soivio, Laura论文数: 0 引用数: 0 h-index: 0机构: Helsinki Univ Hosp, Pediat Neuropsychiat Unit, Helsinki, Finland Univ Helsinki, Neurosci Ctr, Helsinki, FinlandHennah, William论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Neurosci Ctr, Helsinki, Finland Univ Helsinki, Neurosci Ctr, Helsinki, Finland
- [6] Common genetic variants contribute to risk of rare severe neurodevelopmental disordersNature, 2018, 562 : 268 - 271Mari E. K. Niemi论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsHilary C. Martin论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsDaniel L. Rice论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsGiuseppe Gallone论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsScott Gordon论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsMartin Kelemen论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsKerrie McAloney论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsJeremy McRae论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsElizabeth J. Radford论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsSui Yu论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsJozef Gecz论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsNicholas G. Martin论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsCaroline F. Wright论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsDavid R. Fitzpatrick论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsHelen V. Firth论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsMatthew E. Hurles论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of PaediatricsJeffrey C. Barrett论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Institute,Department of Paediatrics
- [7] Common genetic variants contribute to risk of rare severe neurodevelopmental disordersNATURE, 2018, 562 (7726) : 268 - +Niemi, Mari E. K.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandMartin, Hilary C.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandRice, Daniel L.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandGallon, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandGordon, Scott论文数: 0 引用数: 0 h-index: 0机构: QIMR Berghofer Med Res Inst, Brisbane, Qld, Australia Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandKelemen, Martin论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandMcAloney, Kerrie论文数: 0 引用数: 0 h-index: 0机构: QIMR Berghofer Med Res Inst, Brisbane, Qld, Australia Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandMcRae, Jeremy论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandRadford, Elizabeth J.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England Univ Cambridge, Dept Paediat, Cambridge, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandYu, Sui论文数: 0 引用数: 0 h-index: 0机构: Womens & Childrens Hosp, Dept Genet & Mol Pathol, SA Pathol, Adelaide, SA, Australia Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandGecz, Jozef论文数: 0 引用数: 0 h-index: 0机构: Univ Adelaide, Fac Hlth & Med Sci, Adelaide Med Sch, Adelaide, SA, Australia Univ Adelaide, Fac Hlth & Med Sci, Robinson Res Inst, Adelaide, SA, Australia South Australian Hlth & Med Res Inst, Adelaide, SA, Australia Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandMartin, Nicholas G.论文数: 0 引用数: 0 h-index: 0机构: QIMR Berghofer Med Res Inst, Brisbane, Qld, Australia Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandWright, Caroline F.论文数: 0 引用数: 0 h-index: 0机构: Univ Exeter, Royal Devon & Exeter Hosp, Inst Biomed & Clin Sci, Med Sch,RILD, Exeter, Devon, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandFitzpatrick, David R.论文数: 0 引用数: 0 h-index: 0机构: Univ Edinburgh, Western Gen Hosp, MRC Human Genet Unit, MRC IGMM, Edinburgh, Midlothian, Scotland Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandFirth, Helen, V论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England Cambridge Univ Hosp NHS Fdn Trust, Dept Clin Genet, Cambridge, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandHurles, Matthew E.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, EnglandBarrett, Jeffrey C.论文数: 0 引用数: 0 h-index: 0机构: Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England Wellcome Sanger Inst, Wellcome Genome Campus, Hinxton, England
- [8] Rare heterozygous genetic variants of NRXN and NLGN gene families involved in synaptic function and their association with neurodevelopmental disordersDEVELOPMENTAL NEUROBIOLOGY, 2024, 84 (03) : 158 - 168Gerik-Celebi, Hamide Betul论文数: 0 引用数: 0 h-index: 0机构: Balikesir Ataturk City Hosp, Dept Med Genet, Balikesir, Turkiye Balikesir Ataturk City Hosp, Dept Med Genet, Balikesir, TurkiyeBolat, Hilmi论文数: 0 引用数: 0 h-index: 0机构: Balikesir Univ, Fac Med, Dept Med Genet, Balikesir, Turkiye Balikesir Univ, Dept Med Genet, Cagis Kampus, Balikesir, Turkiye Balikesir Ataturk City Hosp, Dept Med Genet, Balikesir, TurkiyeUnsel-Bolat, Gul论文数: 0 引用数: 0 h-index: 0机构: Balikesir Univ, Fac Med, Dept Child & Adolescent Psychiat, Balikesir, Turkiye Balikesir Ataturk City Hosp, Dept Med Genet, Balikesir, Turkiye
- [9] Frequency and association of mitochondrial genetic variants with neurological disordersMITOCHONDRION, 2019, 46 : 345 - 360Cruz, Ana Carolina P.论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catolica Paranci PUCPR, Expt Multiuser Lab LEM, Grad Program Hlth Sci PPGCS, Sch Med PPGCS, BR-80215901 Curitiba, Parana, Brazil Pontificia Univ Catolica Paranci PUCPR, Expt Multiuser Lab LEM, Grad Program Hlth Sci PPGCS, Sch Med PPGCS, BR-80215901 Curitiba, Parana, BrazilFerrasa, Adriano论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catolica Paranci PUCPR, Expt Multiuser Lab LEM, Grad Program Hlth Sci PPGCS, Sch Med PPGCS, BR-80215901 Curitiba, Parana, Brazil UEPG, Dept Informat DEINFO, BR-84030900 Ponta Grosso, Parana, Brazil Pontificia Univ Catolica Paranci PUCPR, Expt Multiuser Lab LEM, Grad Program Hlth Sci PPGCS, Sch Med PPGCS, BR-80215901 Curitiba, Parana, BrazilMuotri, Alysson R.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Rady Childrens Hosp San Diego, Dept Cellular & Mol Med, Sch Med,Dept Pediat,Stem Cell Program, La Jolla, CA 92037 USA Pontificia Univ Catolica Paranci PUCPR, Expt Multiuser Lab LEM, Grad Program Hlth Sci PPGCS, Sch Med PPGCS, BR-80215901 Curitiba, Parana, BrazilHerai, Roberto H.论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catolica Paranci PUCPR, Expt Multiuser Lab LEM, Grad Program Hlth Sci PPGCS, Sch Med PPGCS, BR-80215901 Curitiba, Parana, Brazil Lico Kaesemodel Inst ILK, BR-80240000 Curitiba, Parana, Brazil Pontificia Univ Catolica Paranci PUCPR, Expt Multiuser Lab LEM, Grad Program Hlth Sci PPGCS, Sch Med PPGCS, BR-80215901 Curitiba, Parana, Brazil
- [10] The association between screen time and genetic risks for neurodevelopmental disorders in childrenPSYCHIATRY RESEARCH, 2023, 327Takahashi, Nagahide论文数: 0 引用数: 0 h-index: 0机构: Nagoya Univ, Grad Sch Med, Dept Child & Adolescent Psychiat, 65 Tsuruma Cho,Showa Ku, Nagoya, Aichi 4668550, Japan Hamamatsu Univ Sch Med, Res Ctr Child Mental Dev, Hamamatsu, Japan Hamamatsu Univ Sch Med, Osaka Univ, Kanazawa Univ, United Grad Sch Child Dev,Chiba Univ, Hamamatsu, Japan Univ Fukui, Fukui, Japan Nagoya Univ, Grad Sch Med, Dept Child & Adolescent Psychiat, 65 Tsuruma Cho,Showa Ku, Nagoya, Aichi 4668550, JapanTsuchiya, Kenji J.论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Res Ctr Child Mental Dev, Hamamatsu, Japan Hamamatsu Univ Sch Med, Osaka Univ, Kanazawa Univ, United Grad Sch Child Dev,Chiba Univ, Hamamatsu, Japan Univ Fukui, Fukui, Japan Nagoya Univ, Grad Sch Med, Dept Child & Adolescent Psychiat, 65 Tsuruma Cho,Showa Ku, Nagoya, Aichi 4668550, JapanOkumura, Akemi论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Res Ctr Child Mental Dev, Hamamatsu, Japan Hamamatsu Univ Sch Med, Osaka Univ, Kanazawa Univ, United Grad Sch Child Dev,Chiba Univ, Hamamatsu, Japan Univ Fukui, Fukui, Japan Nagoya Univ, Grad Sch Med, Dept Child & Adolescent Psychiat, 65 Tsuruma Cho,Showa Ku, Nagoya, Aichi 4668550, JapanHarada, Taeko论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Res Ctr Child Mental Dev, Hamamatsu, Japan Hamamatsu Univ Sch Med, Osaka Univ, Kanazawa Univ, United Grad Sch Child Dev,Chiba Univ, Hamamatsu, Japan Univ Fukui, Fukui, Japan Nagoya Univ, Grad Sch Med, Dept Child & Adolescent Psychiat, 65 Tsuruma Cho,Showa Ku, Nagoya, Aichi 4668550, Japan论文数: 引用数: h-index:机构:Rahman, Md Shafiur论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Res Ctr Child Mental Dev, Hamamatsu, Japan Hamamatsu Univ Sch Med, Osaka Univ, Kanazawa Univ, United Grad Sch Child Dev,Chiba Univ, Hamamatsu, Japan Univ Fukui, Fukui, Japan Nagoya Univ, Grad Sch Med, Dept Child & Adolescent Psychiat, 65 Tsuruma Cho,Showa Ku, Nagoya, Aichi 4668550, JapanKuwabara, Hitoshi论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Res Ctr Child Mental Dev, Hamamatsu, Japan Hamamatsu Univ Sch Med, Osaka Univ, Kanazawa Univ, United Grad Sch Child Dev,Chiba Univ, Hamamatsu, Japan Univ Fukui, Fukui, Japan Saitama Med Univ, Dept Psychiat, Saitama, Japan Nagoya Univ, Grad Sch Med, Dept Child & Adolescent Psychiat, 65 Tsuruma Cho,Showa Ku, Nagoya, Aichi 4668550, JapanNomura, Yoko论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Res Ctr Child Mental Dev, Hamamatsu, Japan CUNY, Queens Coll, New York, NY USA CUNY, Grad Ctr, New York, NY USA Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY USA Nagoya Univ, Grad Sch Med, Dept Child & Adolescent Psychiat, 65 Tsuruma Cho,Showa Ku, Nagoya, Aichi 4668550, JapanNishimura, Tomoko论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Res Ctr Child Mental Dev, Hamamatsu, Japan Hamamatsu Univ Sch Med, Osaka Univ, Kanazawa Univ, United Grad Sch Child Dev,Chiba Univ, Hamamatsu, Japan Univ Fukui, Fukui, Japan Nagoya Univ, Grad Sch Med, Dept Child & Adolescent Psychiat, 65 Tsuruma Cho,Showa Ku, Nagoya, Aichi 4668550, Japan