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For: Dentici ML, Niceta M, Pantaleoni F, Barresi S, Bencivenga P, Dallapiccola B, Digilio MC, Tartaglia M. Expanding the phenotypic spectrum of truncating POGZ mutations: Association with CNS malformations, skeletal abnormalities, and distinctive facial dysmorphism. Am J Med Genet A 2017;173:1965-9. [PMID: 28480548 DOI: 10.1002/ajmg.a.38255] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 3.2] [Reference Citation Analysis]
Number Citing Articles
1 Deng L, Mojica-perez SP, Azaria RD, Schultz M, Parent JM, Niu W. Loss of POGZ alters neural differentiation of human embryonic stem cells. Molecular and Cellular Neuroscience 2022. [DOI: 10.1016/j.mcn.2022.103727] [Reference Citation Analysis]
2 Nagy D, Verheyen S, Wigby KM, Borovikov A, Sharkov A, Slegesky V, Larson A, Fagerberg C, Brasch-andersen C, Kibæk M, Bader I, Hernan R, High FA, Chung WK, Schieving JH, Behunova J, Smogavec M, Laccone F, Witsch-baumgartner M, Zobel J, Duba H, Weis D. Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring. Genes 2022;13:154. [DOI: 10.3390/genes13010154] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
3 Heath J, Cheyou ES, Findlay S, Luo VM, Carpio EP, Lee J, Djerir B, Chen X, Morin T, Lebeau B, Karam M, Bagci H, Grapton D, Ursini-Siegel J, Côté JF, Witcher M, Richard S, Maréchal A, Orthwein A. POGZ promotes homology-directed DNA repair in an HP1-dependent manner. EMBO Rep 2021;:e51041. [PMID: 34758190 DOI: 10.15252/embr.202051041] [Reference Citation Analysis]
4 Frewer V, Gilchrist CP, Collins SE, Williams K, Seal ML, Leventer RJ, Amor DJ. A systematic review of brain MRI findings in monogenic disorders strongly associated with autism spectrum disorder. J Child Psychol Psychiatry 2021;62:1339-52. [PMID: 34426966 DOI: 10.1111/jcpp.13510] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Donnarumma B, Riccio MP, Terrone G, Palma M, Strisciuglio P, Scala I. Expanding the neurological and behavioral phenotype of White-Sutton syndrome: a case report. Ital J Pediatr 2021;47:148. [PMID: 34215294 DOI: 10.1186/s13052-021-01101-9] [Reference Citation Analysis]
6 Trimarchi G, Caraffi SG, Radio FC, Barresi S, Contrò G, Pizzi S, Maini I, Pollazzon M, Fusco C, Sassi S, Nicoli D, Napoli M, Pascarella R, Gargano G, Zuffardi O, Tartaglia M, Garavelli L. Adducted Thumb and Peripheral Polyneuropathy: Diagnostic Supports in Suspecting White-Sutton Syndrome: Case Report and Review of the Literature. Genes (Basel) 2021;12:950. [PMID: 34206215 DOI: 10.3390/genes12070950] [Reference Citation Analysis]
7 Liu S, Yan Z, Huang Y, Zheng W, Deng Y, Zou Y, Xie H. A case of White-Sutton syndrome arising from a maternally-inherited mutation in POGZ. Psychiatr Genet 2021;31:135-9. [PMID: 34133408 DOI: 10.1097/YPG.0000000000000288] [Reference Citation Analysis]
8 Türay S, Eröz R. White-Sutton syndrome with hot water epilepsy and coexistence of SHOX gene variations. Acta Neurol Belg 2021;121:749-55. [PMID: 33837909 DOI: 10.1007/s13760-021-01671-9] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Wright CM, Guter SJ, Cook EH. Case Report: Association of Comorbid Psychiatric Disorders and Sigmoid Prolapse with de novo POGZ Mutation. J Autism Dev Disord 2021. [PMID: 33909211 DOI: 10.1007/s10803-021-05032-6] [Reference Citation Analysis]
10 Dal S, Hopper B, du Chattel MVR, Goel H. A case of White-Sutton syndrome with previously described loss-of-function variant in DDE domain of POGZ (p.Arg1211*) and Kartagener syndrome. Am J Med Genet A 2021;185:1006-7. [PMID: 33377604 DOI: 10.1002/ajmg.a.62042] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
11 Garde A, Cornaton J, Sorlin A, Moutton S, Nicolas C, Juif C, Geneviève D, Perrin L, Khau-Van-Kien P, Smol T, Vincent-Delorme C, Isidor B, Cogné B, Afenjar A, Keren B, Coubes C, Prieur F, Toutain A, Trousselet Y, Bourgouin S, Gonin-Olympiade C, Giraudat K, Piton A, Gérard B, Odent S, Tessier F, Lemasson L, Heide S, Gelineau AC, Sarret C, Miret A, Schaefer E, Piard J, Mathevet R, Boucon M, Bruel AL, Mau-Them FT, Chevarin M, Vitobello A, Philippe C, Thauvin-Robinet C, Faivre L. Neuropsychological study in 19 French patients with White-Sutton syndrome and POGZ mutations. Clin Genet 2021;99:407-17. [PMID: 33277917 DOI: 10.1111/cge.13894] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
12 Cunniff MM, Markenscoff-Papadimitriou E, Ostrowski J, Rubenstein JL, Sohal VS. Altered hippocampal-prefrontal communication during anxiety-related avoidance in mice deficient for the autism-associated gene Pogz. Elife 2020;9:e54835. [PMID: 33155545 DOI: 10.7554/eLife.54835] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
13 Pascolini G, Agolini E, Fleischer N, Gulotta E, Cesario C, D'Elia G, Novelli A, Majore S, Grammatico P. A novel patient with White-Sutton syndrome refines the mutational and clinical repertoire of the POGZ-related phenotype and suggests further observations. Am J Med Genet A 2020;182:1791-5. [PMID: 32359026 DOI: 10.1002/ajmg.a.61605] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
14 Samanta D, Ramakrishnaiah R, Schaefer B. The neurological aspects related to POGZ mutation: case report and review of CNS malformations and epilepsy. Acta Neurol Belg 2020;120:447-50. [PMID: 30879264 DOI: 10.1007/s13760-019-01122-6] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 6.5] [Reference Citation Analysis]
15 Matsumura K, Seiriki K, Okada S, Nagase M, Ayabe S, Yamada I, Furuse T, Shibuya H, Yasuda Y, Yamamori H, Fujimoto M, Nagayasu K, Yamamoto K, Kitagawa K, Miura H, Gotoda-Nishimura N, Igarashi H, Hayashida M, Baba M, Kondo M, Hasebe S, Ueshima K, Kasai A, Ago Y, Hayata-Takano A, Shintani N, Iguchi T, Sato M, Yamaguchi S, Tamura M, Wakana S, Yoshiki A, Watabe AM, Okano H, Takuma K, Hashimoto R, Hashimoto H, Nakazawa T. Pathogenic POGZ mutation causes impaired cortical development and reversible autism-like phenotypes. Nat Commun 2020;11:859. [PMID: 32103003 DOI: 10.1038/s41467-020-14697-z] [Cited by in Crossref: 17] [Cited by in F6Publishing: 28] [Article Influence: 8.5] [Reference Citation Analysis]
16 Assia Batzir N, Posey JE, Song X, Akdemir ZC, Rosenfeld JA, Brown CW, Chen E, Holtrop SG, Mizerik E, Nieto Moreno M, Payne K, Raas-Rothschild A, Scott R, Vernon HJ, Zadeh N, Lupski JR, Sutton VR; Baylor-Hopkins Center for Mendelian Genomics. Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome). Am J Med Genet A 2020;182:38-52. [PMID: 31782611 DOI: 10.1002/ajmg.a.61380] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 4.3] [Reference Citation Analysis]
17 Hansen AW, Murugan M, Li H, Khayat MM, Wang L, Rosenfeld J, Andrews BK, Jhangiani SN, Coban Akdemir ZH, Sedlazeck FJ, Ashley-Koch AE, Liu P, Muzny DM, Davis EE, Katsanis N, Sabo A, Posey JE, Yang Y, Wangler MF, Eng CM, Sutton VR, Lupski JR, Boerwinkle E, Gibbs RA; Task Force for Neonatal Genomics. A Genocentric Approach to Discovery of Mendelian Disorders. Am J Hum Genet 2019;105:974-86. [PMID: 31668702 DOI: 10.1016/j.ajhg.2019.09.027] [Cited by in Crossref: 19] [Cited by in F6Publishing: 14] [Article Influence: 6.3] [Reference Citation Analysis]
18 Ferretti A, Barresi S, Trivisano M, Ciolfi A, Dentici ML, Radio FC, Vigevano F, Tartaglia M, Specchio N. POGZ-related epilepsy: Case report and review of the literature. Am J Med Genet A 2019;179:1631-6. [PMID: 31136090 DOI: 10.1002/ajmg.a.61206] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.7] [Reference Citation Analysis]