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- [1] Gain-of-function variants in the ODC1 gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalitiesAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (12) : 2554 - 2560Rodan, Lance H.论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA Harvard Med Sch, Boston Childrens Hosp, Dept Neurol, Boston, MA USA Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USAAnyane-Yeboa, Kwame论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pediat, Med Ctr, Div Clin Genet, New York, NY 10027 USA Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USAChong, Karen论文数: 0 引用数: 0 h-index: 0机构: Univ Toronto, Mt Sinai Hosp, Dept Obstet & Gynecol, Prenatal Diag & Med Genet Program, Toronto, ON, Canada Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USAWassink-Ruiter, Jolien S. Klein论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USAWilson, Ashley论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pediat, Med Ctr, Div Clin Genet, New York, NY 10027 USA Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USASmith, Lacey论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Epilepsy & Clin Neurophysiol, Dept Neurol, Epilepsy Genet Program, Boston, MA USA Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USAKothare, Sanjeev V.论文数: 0 引用数: 0 h-index: 0机构: Northwell Hlth, Zucker Sch Med Hofstra Northwell, Dept Neurol, New York, NY USA Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USARajabi, Farrah论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA论文数: 引用数: h-index:机构:Ni, Min论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr, Childrens Med Ctr, Res Inst, Dallas, TX USA Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USADeBerardinis, Ralph J.论文数: 0 引用数: 0 h-index: 0机构: Univ Texas Southwestern Med Ctr, Childrens Med Ctr, Res Inst, Dallas, TX USA Univ Texas Southwestern Med Ctr, Howard Hughes Med Inst, Dallas, TX USA Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USAPoduri, Annapurna论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Neurol, Boston, MA USA Boston Childrens Hosp, Div Epilepsy & Clin Neurophysiol, Dept Neurol, Epilepsy Genet Program, Boston, MA USA Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USABerry, Gerard T.论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA
- [2] Role of novel de novo gain-of-function TRPM3 mutations in a spectrum of neurodevelopmental disordersCELL CALCIUM, 2023, 110Kashio, Makiko论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Nat Sci, Natl Inst Physiol Sci, Div Cell Signaling, Okazaki 4448787, Japan Natl Inst Nat Sci, Exploratory Res Ctr Life & Living Syst, Thermal Biol Grp, Okazaki 4448787, Japan Natl Inst Physiol Sci, Div Cell Signaling, 5-1 Higashiyama, Okazaki, Aichi 4448787, Japan Natl Inst Nat Sci, Natl Inst Physiol Sci, Div Cell Signaling, Okazaki 4448787, JapanTominaga, Makoto论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Nat Sci, Natl Inst Physiol Sci, Div Cell Signaling, Okazaki 4448787, Japan Natl Inst Nat Sci, Exploratory Res Ctr Life & Living Syst, Thermal Biol Grp, Okazaki 4448787, Japan Grad Univ Adv Studies SOKENDAI, Dept Physiol Sci, Okazaki 4448585, Japan Natl Inst Physiol Sci, Div Cell Signaling, 5-1 Higashiyama, Okazaki, Aichi 4448787, Japan Natl Inst Nat Sci, Natl Inst Physiol Sci, Div Cell Signaling, Okazaki 4448787, Japan
- [3] Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsyBRAIN, 2022, 145 (04) : 1299 - 1309Ahring, Philip K.论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, Australia Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaLiao, Vivian W. Y.论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, Australia Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, Australia论文数: 引用数: h-index:机构:Johannesen, Katrine M.论文数: 0 引用数: 0 h-index: 0机构: Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Univ Southern Denmark, Dept Reg Hlth Res, Odense, Denmark Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaKrey, Ilona论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Inst Human Genet, Med Ctr, Leipzig, Germany Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, Australia论文数: 引用数: h-index:机构:Stadheim, Barbro F.论文数: 0 引用数: 0 h-index: 0机构: Oslo Univ Hosp, Dept Med Genet, Oslo, Norway Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaDavis, Hannah论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Div Med Genet, Dept Human Genet, Atlanta, GA USA Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaPeinhardt, Charlotte论文数: 0 引用数: 0 h-index: 0机构: Emory Univ, Sch Med, Div Med Genet, Dept Human Genet, Atlanta, GA USA Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaKoko, Mahmoud论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Hertie Inst Clin Brain Res, Dept Neurol & Epileptol, Tubingen, Germany Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaCoorg, Rohini K.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Pediat & Neurol Neurophysiol & Epilepsy, Houston, TX 77030 USA Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaSyrbe, Steffen论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Heidelberg, Ctr Paediat & Adolescent Med, Div Paediat Epileptol, Heidelberg, Germany Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaBertsche, Astrid论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Children & Adolescents, Neuropaediat, Rostock, Germany Univ Hosp Children & Adolescents, Ctr Pediat Res, Leipzig, Germany Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaSantiago-Sim, Teresa论文数: 0 引用数: 0 h-index: 0机构: GeneDx Inc, Gaithersburg, MD 20877 USA Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaDiemer, Tue论文数: 0 引用数: 0 h-index: 0机构: Aalborg Univ Hosp, Dept Clin Genet, Aalborg, Denmark Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaFenger, Christina D.论文数: 0 引用数: 0 h-index: 0机构: Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Univ Southern Denmark, Dept Reg Hlth Res, Odense, Denmark Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaPlatzer, Konrad论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Inst Human Genet, Med Ctr, Leipzig, Germany Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaEichler, Evan E.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA USA Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USA Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaLerche, Holger论文数: 0 引用数: 0 h-index: 0机构: Univ Tubingen, Hertie Inst Clin Brain Res, Dept Neurol & Epileptol, Tubingen, Germany Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaLemke, Johannes R.论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Inst Human Genet, Med Ctr, Leipzig, Germany Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaChebib, Mary论文数: 0 引用数: 0 h-index: 0机构: Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, Australia Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, AustraliaMoller, Rikke S.论文数: 0 引用数: 0 h-index: 0机构: Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Treatment, Dianalund, Denmark Univ Southern Denmark, Dept Reg Hlth Res, Odense, Denmark Univ Sydney, Fac Med & Hlth, Brain & Mind Ctr, Sch Pharm, Sydney, NSW, Australia
- [4] De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathyANNALS OF NEUROLOGY, 2018, 83 (06) : 1198 - 1204论文数: 引用数: h-index:机构:Soldovieri, Maria Virginia论文数: 0 引用数: 0 h-index: 0机构: Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, Italy Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, ItalyBast, Thomas论文数: 0 引用数: 0 h-index: 0机构: Epilepsy Ctr Kork, Kehl, Germany Univ Freiburg, Fac Med, Freiburg, Germany Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, ItalyTurnpenny, Peter D.论文数: 0 引用数: 0 h-index: 0机构: Royal Devon & Exeter NHS Fdn Trust, Clin Genet, Exeter, Devon, England Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, ItalyUhrig, Sabine论文数: 0 引用数: 0 h-index: 0机构: Klinikum Stuttgart, Inst Clin Genet, Stuttgart, Germany Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, ItalyBiskup, Saskia论文数: 0 引用数: 0 h-index: 0机构: CeGaT GmbH, Tubingen, Germany Praxis Humangenet Tubingen, Tubingen, Germany Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, ItalyDoecker, Miriam论文数: 0 引用数: 0 h-index: 0机构: CeGaT GmbH, Tubingen, Germany Praxis Humangenet Tubingen, Tubingen, Germany Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, ItalyFleck, Thilo论文数: 0 引用数: 0 h-index: 0机构: Univ Freiburg, Dept Congenital Heart Dis & Pediat Cardiol, Med Ctr, Univ Heart Ctr Freiburg Bad Krozingen, Freiburg, Germany Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, ItalyMosca, Ilaria论文数: 0 引用数: 0 h-index: 0机构: Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, Italy Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, ItalyManocchio, Laura论文数: 0 引用数: 0 h-index: 0机构: Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, Italy Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, Italy论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Lemke, Johannes R.论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig Hosp & Clin, Inst Human Genet, Philipp Rosenthal Str 55, D-04103 Leipzig, Germany Univ Molise, Dept Med & Hlth Sci Vincenzo Tiberio, Campobasso, Italy
- [5] De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic featuresHuman Genetics, 2016, 135 : 699 - 705Volkan Okur论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsMegan T. Cho论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsLindsay Henderson论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsKyle Retterer论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsMichael Schneider论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsShannon Sattler论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsDmitriy Niyazov论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsMeron Azage论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsSharon Smith论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsJonathan Picker论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsSharyn Lincoln论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsMark Tarnopolsky论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsLauren Brady论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsHans T. Bjornsson论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsCarolyn Applegate论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsAmy Dameron论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsRebecca Willaert论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsBerivan Baskin论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsJane Juusola论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of PediatricsWendy K. Chung论文数: 0 引用数: 0 h-index: 0机构: Columbia University Medical Center,Department of Pediatrics
- [6] De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic featuresHUMAN GENETICS, 2016, 135 (07) : 699 - 705Okur, Volkan论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USACho, Megan T.论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USAHenderson, Lindsay论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USARetterer, Kyle论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USASchneider, Michael论文数: 0 引用数: 0 h-index: 0机构: Carle Phys Grp, Urbana, IL USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USASattler, Shannon论文数: 0 引用数: 0 h-index: 0机构: Carle Phys Grp, Urbana, IL USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USANiyazov, Dmitriy论文数: 0 引用数: 0 h-index: 0机构: Ochsner Clin & Alton Ochsner Med Fdn, New Orleans, LA USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USAAzage, Meron论文数: 0 引用数: 0 h-index: 0机构: Ochsner Clin & Alton Ochsner Med Fdn, New Orleans, LA USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USASmith, Sharon论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USAPicker, Jonathan论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USALincoln, Sharyn论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Div Genet & Genom, Boston, MA USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USATarnopolsky, Mark论文数: 0 引用数: 0 h-index: 0机构: McMaster Childrens Hosp, Dept Pediat, Hamilton, ON, Canada Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USABrady, Lauren论文数: 0 引用数: 0 h-index: 0机构: McMaster Childrens Hosp, Dept Pediat, Hamilton, ON, Canada Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USABjornsson, Hans T.论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, McKusick Nathans Inst Genet Med, Baltimore, MD USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USAApplegate, Carolyn论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, McKusick Nathans Inst Genet Med, Baltimore, MD USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USADameron, Amy论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USAWillaert, Rebecca论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USABaskin, Berivan论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USAJuusola, Jane论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USAChung, Wendy K.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USA Columbia Univ, Med Ctr, Dept Med, New York, NY 10032 USA Columbia Univ, Med Ctr, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USA
- [7] De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic featuresAMERICAN JOURNAL OF HUMAN GENETICS, 2024, 111 (04) : 742 - 760Pan, Xueyang论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Dan Duncan Neurol Res Inst, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USATao, Alice M.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Vagelos Sch Phys & Surg, New York, NY USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USALu, Shenzhao论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Dan Duncan Neurol Res Inst, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAMa, Mengqi论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Dan Duncan Neurol Res Inst, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAHannan, Shabab B.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Dan Duncan Neurol Res Inst, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USASlaugh, Rachel论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, St Louis Sch Med, Dept Pediat, Div Genet & Genom Med, St Louis, MO USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAWilliams, Sarah Drewes论文数: 0 引用数: 0 h-index: 0机构: UPMC Childrens Hosp Pittsburgh, Dept Pediat, Div Genet & Genom Med, Pittsburgh, PA USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAO'Grady, Lauren论文数: 0 引用数: 0 h-index: 0机构: Massachusetts Gen Children, Div Med Genet & Metab, Boston, MA USA MGH Inst Hlth Profess, Charlestown, MA USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAKanca, Oguz论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Dan Duncan Neurol Res Inst, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAPerson, Richard论文数: 0 引用数: 0 h-index: 0机构: GeneDx LLC, Gaithersburg, MD USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USACarter, Melissa T.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Eastern Ontario, Dept Genet, Ottawa, ON, Canada Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAPlatzer, Konrad论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Inst Human Genet, Med Ctr, Leipzig, Germany Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USASchnabel, Franziska论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Inst Human Genet, Med Ctr, Leipzig, Germany Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAAbou Jamra, Rami论文数: 0 引用数: 0 h-index: 0机构: Univ Leipzig, Inst Human Genet, Med Ctr, Leipzig, Germany Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USARoberts, Amy E.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Dept Cardiol, Boston, MA USA Boston Childrens Hosp, Dept Med, Div Genet, Boston, MA USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USANewburger, Jane W.论文数: 0 引用数: 0 h-index: 0机构: Boston Childrens Hosp, Dept Cardiol, Boston, MA USA Harvard Med Sch, Dept Pediat, Boston, MA USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USARevah-Politi, Anya论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Inst Genom Med, Irving Med Ctr, New York, NY USA Columbia Univ, Precis Genom Lab, Irving Med Ctr, New York, NY USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAGranadillo, Jorge L.论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, St Louis Sch Med, Dept Pediat, Div Genet & Genom Med, St Louis, MO USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAStegmann, Alexander P. A.论文数: 0 引用数: 0 h-index: 0机构: Maastricht Univ, Dept Clin Genet, Med Ctr, Maastricht, Netherlands Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USASinnema, Margje论文数: 0 引用数: 0 h-index: 0机构: Maastricht Univ, Dept Clin Genet, Med Ctr, Maastricht, Netherlands Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA论文数: 引用数: h-index:机构:Salpietro, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: UCL, Dept Neuromuscular Disorders, Inst Neurol, Queen Sq, London, England Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USACapra, Valeria论文数: 0 引用数: 0 h-index: 0机构: IRCCS Ist Giannina Gaslini, Unit Med Genet & Genom, Genoa, Italy Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAGhaloul-Gonzalez, Lina论文数: 0 引用数: 0 h-index: 0机构: UPMC Childrens Hosp Pittsburgh, Dept Pediat, Div Genet & Genom Med, Pittsburgh, PA USA Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA论文数: 引用数: h-index:机构:Simon, Marleen E. H.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USASweetser, David A.论文数: 0 引用数: 0 h-index: 0机构: Massachusetts Gen Children, Div Med Genet & Metab, Boston, MA USA Massachusetts Gen Hosp, Ctr Genom Med, Boston, MA USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAGlinton, Kevin E.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Dept Genet, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAKirk, Susan E.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Pediat, Sect Hematol Oncol, Houston, TX USA Texas Childrens Canc & Hematol Ctr, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAWangler, Michael F.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Dan Duncan Neurol Res Inst, Houston, TX USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAYamamoto, Shinya论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Jan & Dan Duncan Neurol Res Inst, Houston, TX USA Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USAChung, Wendy K.论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Dept Pediat, Boston, MA 02115 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USABellen, Hugo J.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
- [8] Heterozygous De Novo UBTF Gain-of-Function Variant Is Associated with Neurodegeneration in ChildhoodAMERICAN JOURNAL OF HUMAN GENETICS, 2017, 101 (02) : 267 - 273Edvardson, Simon论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Pediat Neurol Unit, IL-91120 Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelNicolae, Claudia M.论文数: 0 引用数: 0 h-index: 0机构: Penn State Univ, Coll Med, Dept Biochem & Mol Biol, Hershey, PA 17033 USA Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelAgrawal, Pankaj B.论文数: 0 引用数: 0 h-index: 0机构: Harvard Med Sch, Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Newborn Med, Boston, MA 02115 USA Harvard Med Sch, Boston Childrens Hosp, Manton Ctr Orphan Dis Res, Div Genet & Genom, Boston, MA 02115 USA Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelMignot, Cyril论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Dept Genet, Ctr Reference Deficiences Intellectuelles Causes, F-75013 Paris, France Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelPayne, Katelyn论文数: 0 引用数: 0 h-index: 0机构: Riley Hosp Children, Indianapolis, IN 46202 USA Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelPrasad, Asuri Narayan论文数: 0 引用数: 0 h-index: 0机构: Univ Western Ontario, Dept Pediat, Sect Paediat Neurol, London, ON N6A 3K7, Canada Univ Western Ontario, Div Clin Neurol Sci, Fac Med, Schulich Sch Med & Dent, London, ON N6A 3K7, Canada Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelPrasad, Chitra论文数: 0 引用数: 0 h-index: 0机构: Western Univ, Dept Paediat, Sect Genet, London, ON N6A 3K7, Canada Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelSadler, Laurie论文数: 0 引用数: 0 h-index: 0机构: SUNY Buffalo, Women & Childrens Hosp Buffalo, Dept Pediat, Div Genet,Jacobs Sch Med & Biomed Sci, Buffalo, NY 14214 USA Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, Israel论文数: 引用数: h-index:机构:Mullen, Thomas E.论文数: 0 引用数: 0 h-index: 0机构: Massachusetts Gen Hosp, Analyt & Translat Genet Unit, Boston, MA 53377 USA Broad Inst MIT & Harvard, Program Med & Populat Genet, Cambridge, MA 02142 USA Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelBegtrup, Amber论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD 20877 USA Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelBaskin, Berivan论文数: 0 引用数: 0 h-index: 0机构: GeneDx, Gaithersburg, MD 20877 USA Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelPowis, Zoe论文数: 0 引用数: 0 h-index: 0机构: Ambry Genet, Dept Emerging Genet Med, Aliso Viejo, CA 92656 USA Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelShaag, Avraham论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelKeren, Boris论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, AP HP, Dept Genet, Ctr Reference Deficiences Intellectuelles Causes, F-75013 Paris, France Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelMoldovan, George-Lucian论文数: 0 引用数: 0 h-index: 0机构: Penn State Univ, Coll Med, Dept Biochem & Mol Biol, Hershey, PA 17033 USA Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, IsraelElpeleg, Orly论文数: 0 引用数: 0 h-index: 0机构: Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, Israel Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, IL-91120 Jerusalem, Israel
- [9] MYCN de novo gain-of-function mutation in a patient with a novel megalencephaly syndromeJOURNAL OF MEDICAL GENETICS, 2019, 56 (06) : 388 - 395Kato, Kohji论文数: 0 引用数: 0 h-index: 0机构: Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, Japan Nagoya Univ, Grad Sch Med, Dept Pediat, Nagoya, Aichi, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanMiya, Fuyuki论文数: 0 引用数: 0 h-index: 0机构: Tokyo Med & Dent Univ, Med Res Inst, Dept Med Sci Math, Tokyo, Japan Ctr Integrat Med Sci, Lab Med Sci Math, Tokyo, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanHamada, Nanako论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Inst Dev Res, Dept Mol Neurobiol, Kasugai, Aichi, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanNegishi, Yutaka论文数: 0 引用数: 0 h-index: 0机构: Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanNarumi-Kishimoto, Yoko论文数: 0 引用数: 0 h-index: 0机构: Shimada Ryoiku Ctr Hachiouji, Dept Pediat, Tokyo, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanOzawa, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Shimada Ryoiku Ctr Hachiouji, Dept Pediat, Tokyo, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanIto, Hidenori论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Inst Dev Res, Dept Mol Neurobiol, Kasugai, Aichi, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, Japan论文数: 引用数: h-index:机构:Hattori, Ayako论文数: 0 引用数: 0 h-index: 0机构: Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanOkamoto, Nobuhiko论文数: 0 引用数: 0 h-index: 0机构: Osaka Womens & Childrens Hosp, Dept Med Genet, Osaka, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanKato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Sch Med, Dept Pediat, Tokyo, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanTsunoda, Tatsuhiko论文数: 0 引用数: 0 h-index: 0机构: Tokyo Med & Dent Univ, Med Res Inst, Dept Med Sci Math, Tokyo, Japan Ctr Integrat Med Sci, Lab Med Sci Math, Tokyo, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanKanemura, Yonehiro论文数: 0 引用数: 0 h-index: 0机构: Natl Hosp Org, Osaka Natl Hosp, Inst Clin Res, Div Biomed Res & Innovat, Osaka, Japan Natl Hosp Org, Osaka Natl Hosp, Dept Neurosurg, Osaka, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanKosaki, Kenjiro论文数: 0 引用数: 0 h-index: 0机构: Keio Univ, Sch Med, Ctr Med Genet, Tokyo, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, Japan论文数: 引用数: h-index:机构:Nagata, Koh-ichi论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Inst Dev Res, Dept Mol Neurobiol, Kasugai, Aichi, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, JapanSaitoh, Shinji论文数: 0 引用数: 0 h-index: 0机构: Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, Japan Nagoya City Univ, Grad Sch Med Sci, Dept Pediat & Neonatol, Nagoya, Aichi 4678601, Japan
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