| Year |
Citation |
Score |
| 2022 |
Villa CE, Cheroni C, Dotter CP, López-Tóbon A, Oliveira B, Sacco R, Yahya AÇ, Morandell J, Gabriele M, Tavakoli MR, Lyudchik J, Sommer C, Gabitto M, Danzl JG, Testa G, ... Novarino G, et al. CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectories. Cell Reports. 39: 110615. PMID 35385734 DOI: 10.1016/j.celrep.2022.110615 |
0.367 |
|
| 2021 |
Vasic V, Jones MSO, Haslinger D, Knaus LS, Schmeisser MJ, Novarino G, Chiocchetti AG. Translating the Role of mTOR- and RAS-Associated Signalopathies in Autism Spectrum Disorder: Models, Mechanisms and Treatment. Genes. 12. PMID 34828352 DOI: 10.3390/genes12111746 |
0.308 |
|
| 2020 |
Basilico B, Morandell J, Novarino G. Molecular mechanisms for targeted ASD treatments. Current Opinion in Genetics & Development. 65: 126-137. PMID 32659636 DOI: 10.1016/J.Gde.2020.06.004 |
0.375 |
|
| 2020 |
Parenti I, Rabaneda LG, Schoen H, Novarino G. Neurodevelopmental Disorders: From Genetics to Functional Pathways. Trends in Neurosciences. PMID 32507511 DOI: 10.1016/J.Tins.2020.05.004 |
0.457 |
|
| 2019 |
Knaus L, Tarlungeanu D, Novarino G. S.16.03 A homozygous missense mutation in SLC7A5 leads to autism spectrum disorder and microcephaly European Neuropsychopharmacology. 29: S11. DOI: 10.1016/J.Euroneuro.2019.01.022 |
0.411 |
|
| 2018 |
Deliu E, Arecco N, Morandell J, Dotter CP, Contreras X, Girardot C, Käsper EL, Kozlova A, Kishi K, Chiaradia I, Noh KM, Novarino G. Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition. Nature Neuroscience. PMID 30455454 DOI: 10.1038/S41593-018-0266-2 |
0.385 |
|
| 2018 |
Tărlungeanu DC, Novarino G. Genomics in neurodevelopmental disorders: an avenue to personalized medicine. Experimental & Molecular Medicine. 50: 100. PMID 30089840 DOI: 10.1038/S12276-018-0129-7 |
0.424 |
|
| 2017 |
Sacco R, Cacci E, Novarino G. Neural stem cells in neuropsychiatric disorders. Current Opinion in Neurobiology. 48: 131-138. PMID 29287246 DOI: 10.1016/J.Conb.2017.12.005 |
0.316 |
|
| 2017 |
Marin-Valencia I, Novarino G, Johansen A, Rosti B, Issa MY, Musaev D, Bhat G, Scott E, Silhavy JL, Stanley V, Rosti RO, Gleeson JW, Imam FB, Zaki MS, Gleeson JG. A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features. Journal of Medical Genetics. PMID 28626029 DOI: 10.1136/Jmedgenet-2017-104627 |
0.709 |
|
| 2017 |
Novarino G. Rett syndrome modeling goes simian. Science Translational Medicine. 9. PMID 28592569 DOI: 10.1126/Scitranslmed.Aan8196 |
0.313 |
|
| 2017 |
Schroeder JC, Deliu E, Novarino G, Schmeisser MJ. Genetic and Pharmacological Reversibility of Phenotypes in Mouse Models of Autism Spectrum Disorder. Advances in Anatomy, Embryology, and Cell Biology. 224: 189-211. PMID 28551757 DOI: 10.1007/978-3-319-52498-6_10 |
0.404 |
|
| 2017 |
Hill-Yardin EL, McKeown SJ, Novarino G, Grabrucker AM. Extracerebral Dysfunction in Animal Models of Autism Spectrum Disorder. Advances in Anatomy, Embryology, and Cell Biology. 224: 159-187. PMID 28551756 DOI: 10.1007/978-3-319-52498-6_9 |
0.41 |
|
| 2017 |
Novarino G. Modeling Alzheimer's disease in mice with human neurons. Science Translational Medicine. 9. PMID 28298426 DOI: 10.1126/Scitranslmed.Aam9867 |
0.324 |
|
| 2017 |
Sauerzopf U, Sacco R, Novarino G, Niello M, Weidenauer A, Praschak-Rieder N, Sitte H, Willeit M. Are reprogrammed cells a useful tool for studying dopamine dysfunction in psychotic disorders? A review of the current evidence. The European Journal of Neuroscience. 45: 45-57. PMID 27690184 DOI: 10.1111/Ejn.13418 |
0.359 |
|
| 2017 |
Novarino G. The science of love in ASD and ADHD Science Translational Medicine. 9: eaap8168. DOI: 10.1126/Scitranslmed.Aap8168 |
0.304 |
|
| 2017 |
Novarino G. The riddle of
CHD8
haploinsufficiency in autism spectrum disorder Science Translational Medicine. 9: eaao0972. DOI: 10.1126/Scitranslmed.Aao0972 |
0.324 |
|
| 2016 |
Tărlungeanu DC, Deliu E, Dotter CP, Kara M, Janiesch PC, Scalise M, Galluccio M, Tesulov M, Morelli E, Sonmez FM, Bilguvar K, Ohgaki R, Kanai Y, Johansen A, Esharif S, ... ... Novarino G, et al. Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder. Cell. 167: 1481-1494.e18. PMID 27912058 DOI: 10.1016/J.Cell.2016.11.013 |
0.566 |
|
| 2015 |
Kuechler A, Zink AM, Wieland T, Lüdecke HJ, Cremer K, Salviati L, Magini P, Najafi K, Zweier C, Czeschik JC, Aretz S, Endele S, Tamburrino F, Pinato C, Clementi M, ... ... Novarino G, et al. Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome. European Journal of Human Genetics : Ejhg. 23: 753-60. PMID 25138099 DOI: 10.1038/Ejhg.2014.165 |
0.43 |
|
| 2014 |
Baek ST, Kerjan G, Bielas SL, Lee JE, Fenstermaker AG, Novarino G, Gleeson JG. Off-target effect of doublecortin family shRNA on neuronal migration associated with endogenous microRNA dysregulation. Neuron. 82: 1255-62. PMID 24945770 DOI: 10.1016/J.Neuron.2014.04.036 |
0.662 |
|
| 2014 |
Novarino G, Fenstermaker AG, Zaki MS, Hofree M, Silhavy JL, Heiberg AD, Abdellateef M, Rosti B, Scott E, Mansour L, Masri A, Kayserili H, Al-Aama JY, Abdel-Salam GM, Karminejad A, et al. Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders. Science (New York, N.Y.). 343: 506-11. PMID 24482476 DOI: 10.1126/Science.1247363 |
0.733 |
|
| 2013 |
Novarino G, Baek ST, Gleeson JG. The sacred disease: the puzzling genetics of epileptic disorders. Neuron. 80: 9-11. PMID 24094099 DOI: 10.1016/J.Neuron.2013.09.019 |
0.588 |
|
| 2012 |
Novarino G, El-Fishawy P, Kayserili H, Meguid NA, Scott EM, Schroth J, Silhavy JL, Kara M, Khalil RO, Ben-Omran T, Ercan-Sencicek AG, Hashish AF, Sanders SJ, Gupta AR, Hashem HS, et al. Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy. Science (New York, N.Y.). 338: 394-7. PMID 22956686 DOI: 10.1126/Science.1224631 |
0.574 |
|
| 2012 |
Dixon-Salazar TJ, Silhavy JL, Udpa N, Schroth J, Bielas S, Schaffer AE, Olvera J, Bafna V, Zaki MS, Abdel-Salam GH, Mansour LA, Selim L, Abdel-Hadi S, Marzouki N, Ben-Omran T, ... ... Novarino G, et al. Exome sequencing can improve diagnosis and alter patient management. Science Translational Medicine. 4: 138ra78. PMID 22700954 DOI: 10.1126/scitranslmed.3003544 |
0.627 |
|
| 2011 |
Novarino G, Akizu N, Gleeson JG. Modeling human disease in humans: the ciliopathies. Cell. 147: 70-9. PMID 21962508 DOI: 10.1016/J.Cell.2011.09.014 |
0.708 |
|
| 2010 |
Rickheit G, Wartosch L, Schaffer S, Stobrawa SM, Novarino G, Weinert S, Jentsch TJ. Role of ClC-5 in renal endocytosis is unique among ClC exchangers and does not require PY-motif-dependent ubiquitylation. The Journal of Biological Chemistry. 285: 17595-603. PMID 20351103 DOI: 10.1074/Jbc.M110.115600 |
0.323 |
|
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