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For: Vicente A, Bravo-González LA, López-Romero A, Muñoz CS, Sánchez-Meca J. Craniofacial morphology in down syndrome: a systematic review and meta-analysis. Sci Rep 2020;10:19895. [PMID: 33199843 DOI: 10.1038/s41598-020-76984-5] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Syed Mohamed AMF, Wei TZ, Sean CJ, Rosli TI. Comparison of the malocclusion and orthodontic treatment needs of Down syndrome and non-syndromic subjects by using the dental aesthetics index. Spec Care Dentist 2022. [PMID: 36269010 DOI: 10.1111/scd.12790] [Reference Citation Analysis]
2 Llambrich S, González-Colom R, Wouters J, Roldán J, Salassa S, Wouters K, Van Bulck V, Sharpe J, Callaerts-Vegh Z, Vande Velde G, Martínez-Abadías N. Green Tea Catechins Modulate Skeletal Development with Effects Dependent on Dose, Time, and Structure in a down Syndrome Mouse Model. Nutrients 2022;14. [PMID: 36235819 DOI: 10.3390/nu14194167] [Reference Citation Analysis]
3 Redhead Y, Gibbins D, Lana-elola E, Watson-scales S, Dobson L, Krause M, Liu KJ, Fisher EMC, Green JB, Tybulewicz VL. Craniofacial dysmorphology in Down Syndrome is caused by increased dosage of Dyrk1a and at least three other genes.. [DOI: 10.1101/2022.06.27.497841] [Reference Citation Analysis]
4 Campos PSSL, Taitson PF, Pinto da Silva LC, Leão LL. Dental and health aspects in the co-occurrence of Treacher Collins and Down syndromes: Case report. Spec Care Dentist 2022. [PMID: 35667009 DOI: 10.1111/scd.12735] [Reference Citation Analysis]
5 Alam MK, Alfawzan AA, Srivastava KC, Shrivastava D, Ganji KK, Manay SM. Craniofacial morphology in Apert syndrome: a systematic review and meta-analysis. Sci Rep 2022;12:5708. [PMID: 35383244 DOI: 10.1038/s41598-022-09764-y] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Earley MA, Sher ET, Hill TL. Otolaryngologic Disease in Down syndrome. Pediatr Clin North Am 2022;69:381-401. [PMID: 35337546 DOI: 10.1016/j.pcl.2022.01.005] [Reference Citation Analysis]
7 Stanbouly D, Steinberg B, Chuang SK. What are the Soft Tissue Risk Factors for Obstructive Sleep Apnea in Patients with Down's Syndrome? Cleft Palate Craniofac J 2022;:10556656221088171. [PMID: 35306875 DOI: 10.1177/10556656221088171] [Reference Citation Analysis]
8 Ganguly BB. Implications of trisomy 21 on congenital features and health aspects. Genetics and Neurobiology of Down Syndrome 2022. [DOI: 10.1016/b978-0-323-90456-8.00009-0] [Reference Citation Analysis]
9 Ganguly BB. Development of specific phenotypes and genetic consequences in Down syndrome. Genetics and Neurobiology of Down Syndrome 2022. [DOI: 10.1016/b978-0-323-90456-8.00002-8] [Reference Citation Analysis]
10 Lana-Elola E, Cater H, Watson-Scales S, Greenaway S, Müller-Winkler J, Gibbins D, Nemes M, Slender A, Hough T, Keskivali-Bond P, Scudamore CL, Herbert E, Banks GT, Mobbs H, Canonica T, Tosh J, Noy S, Llorian M, Nolan PM, Griffin JL, Good M, Simon M, Mallon AM, Wells S, Fisher EMC, Tybulewicz VLJ. Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes. Dis Model Mech 2021;14:dmm049157. [PMID: 34477842 DOI: 10.1242/dmm.049157] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
11 Ponroy Bally B, Murai KK. Astrocytes in Down Syndrome Across the Lifespan. Front Cell Neurosci 2021;15:702685. [PMID: 34483840 DOI: 10.3389/fncel.2021.702685] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
12 Chen XQ, Xing Z, Chen QD, Salvi RJ, Zhang X, Tycko B, Mobley WC, Yu YE. Mechanistic Analysis of Age-Related Clinical Manifestations in Down Syndrome. Front Aging Neurosci 2021;13:700280. [PMID: 34276349 DOI: 10.3389/fnagi.2021.700280] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
13 Lana-elola E, Cater H, Watson-scales S, Greenaway S, Müller-winkler J, Gibbins D, Nemes M, Slender A, Hough T, Keskivali-bond P, Scudamore CL, Herbert E, Banks GT, Mobbs H, Canonica T, Tosh J, Noy S, Llorian M, Nolan PM, Griffin JL, Good M, Simon M, Mallon A, Wells S, Fisher EMC, Tybulewicz VLJ. Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down Syndrome-related phenotypes.. [DOI: 10.1101/2021.02.11.430828] [Reference Citation Analysis]