BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: El Bouchikhi I, Belhassan K, Moufid FZ, Iraqui Houssaini M, Bouguenouch L, Samri I, Atmani S, Ouldim K. Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate. Int J Pediatr Adolesc Med. 2016;3:133-142. [PMID: 30805484 DOI: 10.1016/j.ijpam.2016.06.003] [Cited by in Crossref: 28] [Cited by in F6Publishing: 24] [Article Influence: 4.7] [Reference Citation Analysis]
Number Citing Articles
1 Geoffray MM, Falissard B, Green J, Kerr B, Evans DG, Huson S, Burkitt-Wright E, Garg S. Autism Spectrum Disorder Symptom Profile Across the RASopathies. Front Psychiatry 2020;11:585700. [PMID: 33519543 DOI: 10.3389/fpsyt.2020.585700] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Gurusamy N, Rajasingh S, Sigamani V, Rajasingh R, Isai DG, Czirok A, Bittel D, Rajasingh J. Noonan syndrome patient-specific induced cardiomyocyte model carrying SOS1 gene variant c.1654A>G. Exp Cell Res 2021;400:112508. [PMID: 33549576 DOI: 10.1016/j.yexcr.2021.112508] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Leach NT, Wilson Mathews DR, Rosenblum LS, Zhou Z, Zhu H, Heim RA. Comparative assessment of gene-specific variant distribution in prenatal and postnatal cohorts tested for Noonan syndrome and related conditions. Genet Med 2019;21:417-25. [DOI: 10.1038/s41436-018-0062-0] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
4 Le Quellec A, Edouard T, Audebert-Bellanger S, Pouzet A, Bourdet K, Colson C, Oriot C, Poignant S, Saraux A, Devauchelle-Pensec V. Joint involvement in Noonan syndrome. A retrospective paediatric descriptive study. Joint Bone Spine 2021;89:105270. [PMID: 34534690 DOI: 10.1016/j.jbspin.2021.105270] [Reference Citation Analysis]
5 Kessler D, Gerlach D, Kraut N, McConnell DB. Targeting Son of Sevenless 1: The pacemaker of KRAS. Curr Opin Chem Biol 2021;62:109-18. [PMID: 33848766 DOI: 10.1016/j.cbpa.2021.02.014] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
6 Radtke HB, Lalor LE, Basel DG, Siegel DH. Clinical Implications of Mosaicism and Low-Level Mosaicism in Neurocutaneous Disorders. Curr Genet Med Rep 2020;8:132-9. [DOI: 10.1007/s40142-020-00193-9] [Reference Citation Analysis]
7 Nees SN, Chung WK. Genetic Basis of Human Congenital Heart Disease. Cold Spring Harb Perspect Biol 2020;12:a036749. [PMID: 31818857 DOI: 10.1101/cshperspect.a036749] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
8 Malniece I, Grasmane A, Inashkina I, Stavusis J, Kreile M, Miklasevics E, Gailite L. The Fetal Phenotype of Noonan Syndrome Caused by Severe, Cancer-Related PTPN11 Variants. Am J Case Rep 2020;21:e922468. [PMID: 32794475 DOI: 10.12659/AJCR.922468] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
9 Khan A, Soliman MAR, Ghannam MM, Jowdy PK, Hess R, Recker MJ, Reynolds RM. Spinal cord glioblastoma multiforme in a patient with Noonan syndrome: A clinical report. Clin Neurol Neurosurg 2021;207:106725. [PMID: 34153779 DOI: 10.1016/j.clineuro.2021.106725] [Reference Citation Analysis]
10 Kushi R, Hirota Y, Ogawa W. Insulin resistance and exaggerated insulin sensitivity triggered by single-gene mutations in the insulin signaling pathway. Diabetol Int 2021;12:62-7. [PMID: 33479580 DOI: 10.1007/s13340-020-00455-5] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
11 Ly R, Soulat G, Iserin L, Ladouceur M. Coronary artery disease in adults with Noonan syndrome: Case series and literature review. Arch Cardiovasc Dis 2021;114:598-605. [PMID: 34535417 DOI: 10.1016/j.acvd.2021.06.006] [Reference Citation Analysis]
12 Hou H, Wang X, Ding W, Xiao C, Cai X, Lv W, Tu Y, Zhao W, Yao J, Yang C. Whole‐genome sequencing reveals the artificial selection and local environmental adaptability of pigeons ( Columba livia ). Evol Appl. [DOI: 10.1111/eva.13284] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Montero-Bullón JF, González-Velasco Ó, Isidoro-García M, Lacal J. Integrated in silico MS-based phosphoproteomics and network enrichment analysis of RASopathy proteins. Orphanet J Rare Dis 2021;16:303. [PMID: 34229750 DOI: 10.1186/s13023-021-01934-x] [Reference Citation Analysis]
14 Libraro A, D'Ascanio V, Cappa M, Chiarito M, Digilio MC, Einaudi S, Grandone A, Maghnie M, Mazzanti L, Mussa A, Patti G, Scarano E, Spinuzza A, Vannelli S, Wasniewska MG, Ferrero GB, Faienza MF. Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height. Front Endocrinol (Lausanne) 2021;12:761171. [PMID: 35002956 DOI: 10.3389/fendo.2021.761171] [Reference Citation Analysis]
15 Qiu Z, Chang WT, Chou YC, Wen KC, Ziying Y, Yuen K, Cai X, Chang TY, Lai HC, Sung PL. Prenatal case of RIT1 mutation associated Noonan syndrome by whole exome sequencing (WES) and review of the literature. Taiwan J Obstet Gynecol 2022;61:535-8. [PMID: 35595454 DOI: 10.1016/j.tjog.2022.03.025] [Reference Citation Analysis]
16 El Bouchikhi I, Bouguenouch L, Moufid FZ, Samri I, Abdouss F, Melhouf MA, Iraqui Houssaini M, Belhassan K, Atmani S, Ouldim K. Molecular and environmental characterization of Noonan syndrome in Morocco reveals a significant association with consanguinity and advanced parental age. Egypt J Med Hum Genet 2020;21. [DOI: 10.1186/s43042-020-0047-9] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
17 Brinkmann J, Lissewski C, Pinna V, Vial Y, Pantaleoni F, Lepri F, Daniele P, Burnyte B, Cuturilo G, Fauth C, Gezdirici A, Kotzot D, Güleç EY, Iotova V, Schanze D, Ramond F, Havlovicová M, Utine GE, Simsek-Kiper PO, Stoyanova M, Verloes A, De Luca A, Tartaglia M, Cavé H, Zenker M. The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered. Eur J Hum Genet 2021;29:524-7. [PMID: 33082526 DOI: 10.1038/s41431-020-00743-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
18 Zhao X, Li Z, Wang L, Lan Z, Lin F, Zhang W, Su Z. A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review. BMC Endocr Disord 2021;21:2. [PMID: 33407364 DOI: 10.1186/s12902-020-00666-6] [Reference Citation Analysis]
19 Shin YL. Correlation between genetic heterogeneity and variability for response to growth hormone in Noonan syndrome. Korean J Pediatr 2019;62:412-3. [PMID: 31319646 DOI: 10.3345/kjp.2019.00220] [Reference Citation Analysis]
20 Koh AL, Tan ES, Brett MS, Lai AHM, Jamuar SS, Ng I, Tan EC. The spectrum of genetic variants and phenotypic features of Southeast Asian patients with Noonan syndrome. Mol Genet Genomic Med 2019;7:e00581. [PMID: 30784236 DOI: 10.1002/mgg3.581] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
21 Meier AB, Raj Murthi S, Rawat H, Toepfer CN, Santamaria G, Schmid M, Mastantuono E, Schwarzmayr T, Berutti R, Cleuziou J, Ewert P, Görlach A, Klingel K, Laugwitz KL, Seidman CE, Seidman JG, Moretti A, Wolf CM. Cell cycle defects underlie childhood-onset cardiomyopathy associated with Noonan syndrome. iScience 2022;25:103596. [PMID: 34988410 DOI: 10.1016/j.isci.2021.103596] [Reference Citation Analysis]
22 Johnson C, Burkhart DL, Haigis KM. Classification of KRAS-Activating Mutations and the Implications for Therapeutic Intervention. Cancer Discov 2022;12:913-23. [PMID: 35373279 DOI: 10.1158/2159-8290.CD-22-0035] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Brodehl A, Milting H, Gerull B. Special Issue "Cardiovascular Genetics". Genes (Basel) 2021;12:479. [PMID: 33810227 DOI: 10.3390/genes12040479] [Reference Citation Analysis]
24 Caiazza M, Rubino M, Monda E, Passariello A, Fusco A, Cirillo A, Esposito A, Pierno A, De Fazio F, Pacileo R, Evangelista E, Pacileo G, Russo MG, Limongelli G. Combined PTPN11 and MYBPC3 Gene Mutations in an Adult Patient with Noonan Syndrome and Hypertrophic Cardiomyopathy. Genes (Basel) 2020;11:E947. [PMID: 32824488 DOI: 10.3390/genes11080947] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
25 Chow CA, Campbell KH, Chou JC, Elder RW. Noonan syndrome and pregnancy outcomes. Cardiol Young 2022;:1-5. [PMID: 35034678 DOI: 10.1017/S104795112100514X] [Reference Citation Analysis]
26 Morales-Rosado JA, Singh H, Olson RJ, Larsen BT, Hager MM, Klee EW, Dhamija R. Recurrent ganglioneuroma in PTPN11-associated Noonan syndrome: A case report and literature review. Am J Med Genet A 2021;185:1883-7. [PMID: 33779033 DOI: 10.1002/ajmg.a.62178] [Reference Citation Analysis]
27 Uludağ Alkaya D, Lissewski C, Yeşil G, Zenker M, Tüysüz B. Expanding the clinical phenotype of RASopathies in 38 Turkish patients, including the rare LZTR1, RAF1, RIT1 variants, and large deletion in NF1. Am J Med Genet A 2021. [PMID: 34184824 DOI: 10.1002/ajmg.a.62410] [Reference Citation Analysis]
28 Rodríguez FA, Castellón L, Moreno R, Paez E, Aracena Álvarez MI. Noonan syndrome with multiple Giant cell lesions, management and treatment with surgery and interferon alpha-2a therapy: Case report. Birth Defects Res 2020;112:732-9. [PMID: 32065515 DOI: 10.1002/bdr2.1659] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
29 Dai Y, Yin R, Yang L, Li ZH. Clinical and genetic spectrum of neonatal arrhythmia in a NICU. Transl Pediatr 2021;10:2432-8. [PMID: 34765466 DOI: 10.21037/tp-21-233] [Reference Citation Analysis]
30 Lee TL, Lin PH, Chen PL, Hong JB, Wu CC. Hereditary Hearing Impairment with Cutaneous Abnormalities. Genes (Basel) 2020;12:43. [PMID: 33396879 DOI: 10.3390/genes12010043] [Reference Citation Analysis]
31 Carrasco Salas P, Gómez-Molina G, Carreto-Alba P, Granell-Escobar R, Vázquez-Rico I, León-Justel A. Noonan syndrome: Severe phenotype and PTPN11 mutations. Med Clin (Barc) 2019;152:62-4. [PMID: 29703613 DOI: 10.1016/j.medcli.2018.03.015] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
32 Dempsey E, Homfray T, Simpson JM, Jeffery S, Mansour S, Ostergaard P. Fetal hydrops – a review and a clinical approach to identifying the cause. Expert Opinion on Orphan Drugs 2020;8:51-66. [DOI: 10.1080/21678707.2020.1719827] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
33 Yang LL, Liang SS. Study on pathogenic genes of dwarfism disease by next-generation sequencing. World J Clin Cases 2021; 9(7): 1600-1609 [PMID: 33728303 DOI: 10.12998/wjcc.v9.i7.1600] [Reference Citation Analysis]