Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1985 2
1988 3
1990 2
1993 2
1994 3
1995 1
1996 8
1997 6
1998 6
1999 11
2000 7
2001 13
2002 12
2003 11
2004 13
2005 13
2006 16
2007 30
2008 13
2009 12
2010 27
2011 25
2012 25
2013 30
2014 25
2015 24
2016 23
2017 26
2018 24
2019 12
2020 28
2021 24
2022 19
2023 13
2024 7

Text availability

Article attribute

Article type

Publication date

Search Results

451 results

Results by year

Filters applied: . Clear all
Page 1
Arrhythmias in Williams Syndrome.
Deitch AM, Giacone HM, Chubb H, Algaze CA, Lechich KM, Collins RT. Deitch AM, et al. Am J Cardiol. 2023 May 15;195:91-97. doi: 10.1016/j.amjcard.2023.03.004. Epub 2023 Apr 8. Am J Cardiol. 2023. PMID: 37037070
Williams syndrome (WS) is a congenital, multisystem disorder in which 80% of patients have cardiovascular abnormalities. ...We retrospectively reviewed all patients with WS with ambulatory electrocardiogram (ECG) monitoring at our institution between October 2017 an …
Williams syndrome (WS) is a congenital, multisystem disorder in which 80% of patients have cardiovascular abnormalities. ...We …
Epigenetic aging in Williams syndrome.
Okazaki S, Kimura R, Otsuka I, Tomiwa K, Funabiki Y, Hagiwara M, Murai T, Hishimoto A. Okazaki S, et al. J Child Psychol Psychiatry. 2022 Dec;63(12):1553-1562. doi: 10.1111/jcpp.13613. Epub 2022 Apr 13. J Child Psychol Psychiatry. 2022. PMID: 35416284
BACKGROUND: Williams syndrome (WS) is a rare genetic disorder caused by a microdeletion at the 7q11.23 region and is characterized by diverse symptoms encompassing physical and cognitive features. ...METHODS: We investigated GrimAge, DNAm-based telomere length (DNAm …
BACKGROUND: Williams syndrome (WS) is a rare genetic disorder caused by a microdeletion at the 7q11.23 region and is character …
Williams syndrome deletions and duplications: Genetic windows to understanding anxiety, sociality, autism, and schizophrenia.
Crespi BJ, Procyshyn TL. Crespi BJ, et al. Neurosci Biobehav Rev. 2017 Aug;79:14-26. doi: 10.1016/j.neubiorev.2017.05.004. Epub 2017 May 10. Neurosci Biobehav Rev. 2017. PMID: 28499504 Review.
We describe and evaluate an integrative hypothesis for helping to explain the major neurocognitive features of individuals with Williams syndrome region deletions and duplications. First, we demonstrate how the cognitive differences between Williams syndro …
We describe and evaluate an integrative hypothesis for helping to explain the major neurocognitive features of individuals with Williams …
Anxiety and Spatial Navigation in Williams Syndrome and Down Syndrome.
Farran EK, Hudson KD, Bennett A, Ameen A, Misheva I, Bechlem B, Blades M, Courbois Y. Farran EK, et al. Dev Neuropsychol. 2022 Apr-Jun;47(3):136-157. doi: 10.1080/87565641.2022.2047685. Epub 2022 Mar 14. Dev Neuropsychol. 2022. PMID: 35282728
Individuals with Down Syndrome (DS) and individuals with Williams syndrome (WS) present with poor navigation and elevated anxiety. ...Most individuals were not permitted to travel independently. A relationship between navigation anxiety and SBSOD scores (but …
Individuals with Down Syndrome (DS) and individuals with Williams syndrome (WS) present with poor navigation and elevated anxi …
Mild macrocytosis in Williams-Beuren syndrome.
Yu E, Feinn R, Bona R, Brink B, Sindhar S, Kozel BA, Pober BR. Yu E, et al. Eur J Med Genet. 2020 Mar;63(3):103740. doi: 10.1016/j.ejmg.2019.103740. Epub 2019 Aug 14. Eur J Med Genet. 2020. PMID: 31419598
Providers encountering isolated mild macrocytosis in WBS can consider observation over further workup....
Providers encountering isolated mild macrocytosis in WBS can consider observation over further workup....
Oxytocin and Oxytocin Receptor Gene Regulation in Williams Syndrome: A Systematic Review.
Çalışkan E, Şahin MN, Güldağ MA. Çalışkan E, et al. Yale J Biol Med. 2021 Dec 29;94(4):623-635. eCollection 2021 Dec. Yale J Biol Med. 2021. PMID: 34970101 Free PMC article. Review.
Williams Syndrome (WS) is a rare genetic multisystem disorder that occurs because of a deletion of approximately 25 genes in the 7q11.23 chromosome region. ...We aim to systematically present the data available of OT/OXTR regulation and expression, and the evidence …
Williams Syndrome (WS) is a rare genetic multisystem disorder that occurs because of a deletion of approximately 25 genes in t …
Understanding Number Line Estimation in Williams Syndrome and Down Syndrome.
Simms V, Karmiloff-Smith A, Ranzato E, Van Herwegen J. Simms V, et al. J Autism Dev Disord. 2020 Feb;50(2):583-591. doi: 10.1007/s10803-019-04268-7. J Autism Dev Disord. 2020. PMID: 31705420 Free PMC article.
Previous studies suggest that tasks dependent on the mental number line may be difficult for Williams Syndrome (WS) and Down Syndrome (DS) groups. However, few have directly assessed number line estimation in these groups. ...Differential relationships between numbe …
Previous studies suggest that tasks dependent on the mental number line may be difficult for Williams Syndrome (WS) and Down S …
Clinical Characteristics and Long-Term Outcomes of Midaortic Syndrome.
Patel RS, Nguyen S, Lee MT, Price MD, Krause H, Truong VTT, Sandhu HK, Charlton-Ouw KM, LeMaire SA, Coselli JS, Prakash SK. Patel RS, et al. Ann Vasc Surg. 2020 Jul;66:318-325. doi: 10.1016/j.avsg.2019.12.039. Epub 2020 Jan 7. Ann Vasc Surg. 2020. PMID: 31923594
The etiology of MAS was identified in 6 cases, including genetic syndromes (neurofibromatosis type 1 (2/13), Williams syndrome (1/13), fibromuscular dysplasia (2/13), and Takayasu arteritis (1/13)). ...Extensive disease frequently requires multiple invasive interven …
The etiology of MAS was identified in 6 cases, including genetic syndromes (neurofibromatosis type 1 (2/13), Williams syndrome …
Mapping brain maturation.
Toga AW, Thompson PM, Sowell ER. Toga AW, et al. Trends Neurosci. 2006 Mar;29(3):148-59. doi: 10.1016/j.tins.2006.01.007. Epub 2006 Feb 10. Trends Neurosci. 2006. PMID: 16472876 Free PMC article. Review.
Here, we review recent progress on imaging studies of development. We focus on cortical and subcortical changes observed in healthy children, and contrast them with abnormal developmental changes in early-onset schizophrenia, fetal alcohol syndrome, attention-deficit-hyper …
Here, we review recent progress on imaging studies of development. We focus on cortical and subcortical changes observed in healthy c …
Williams syndrome is an epigenome-regulator disease.
Kitagawa H, Fujiki R, Yoshimura K, Oya H, Kato S. Kitagawa H, et al. Endocr J. 2011;58(2):77-85. doi: 10.1507/endocrj.k10e-393. Epub 2011 Jan 14. Endocr J. 2011. PMID: 21242649 Free article. Review.
By making WSTF-deficient mice, some of the heart defects as well as abnormal calcium metabolism observed in Williams syndrome are attributed to the abnormal chromatin remodeling activity caused by WSTF deficiency. Thus, we would propose to designate Willia …
By making WSTF-deficient mice, some of the heart defects as well as abnormal calcium metabolism observed in Williams syndro …
451 results