Skip directly to search
Skip directly to A to Z list
Skip directly to navigation
Skip directly to page options
Skip directly to site content
Start of Search Controls
Search Form Controls
Search The CDC
submit
CDC A-Z Index
MENU
CDC A-Z
SEARCH
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
#
Search Form Controls
Search The CDC
submit
CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
About
Public Health Genomics Branch
PHGKB Weekly Horizon Scan
Genomics Precision Health Scan
Advanced Molecular Detection Clips
Non-Genomics Precision Health Scan
CDC-authored Publications Scan
Specialized PHGKB
Cancer PHGKB
Diabetes PHGKB
Economic Evaluation PHGKB
Environmental Health PHGKB
Family Health History PHGKB
Health Equity PHGKB
HLBS-PopOmics
Infectious Diseases PHGKB
Implementation Science PHGKB
Neurological Disorders PHGKB
Pharmacogenomics PHGKB
Primary Immune Deficiency Diseases PHGKB
Rare Diseases PHGKB
Reproductive and Child Health PHGKB
All Databases
COVID-19 GPH (47426)
CDC/NIH Web Information Database (32208)
CDC-Authored Genomics and Precision Health Publications Database (6104)
Precision Health Database (63914)
Tier-Classified Guidelines Database (535)
Pathogen Advanced Molecular Detection Database (26916)
All of Us Reports and Publications Database (730)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (227373)
Epigenetic Epidemiology Publications Database (22897)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 21, 2024
. (Total: 63914 Documents since 2012)
All
Cancer
Diabetes
Economic
Equity
Environmental
FHH
HLBS
ID
Implementation
ND
PGx
PI
Rare
RCH
dataset
All
GPH
Non-GPH
Filtered By
:
Select to fine-tune your search
Disease
Gene
Product Type
Category
Year
Previous
Records 1 - 30 (of 36 Records)
Next
Query Trace:
A holistic approach to fragile X syndrome integrated guidance for person-centred care.
Kirsten Johnson et al. J Appl Res Intellect Disabil 2024 37(3) e13214
Similar articles in PubMed
Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in Chile.
M Cecilia Poli et al. Eur J Hum Genet 2024
Similar articles in PubMed
Ethical issues of involving people with intellectual disabilities in genomic research: a scoping review protocol.
Dorothy Chepkirui et al. Wellcome Open Res 2023 8340
Similar articles in PubMed
Project Inclusive Genetics: Protecting reproductive autonomy from bias via prenatal patient-centered counseling.
Apolline Jungels et al. HGG Adv 2023 4(4) 100228
Similar articles in PubMed
Genome-Wide Sequencing Modalities for Children with Unexplained Global Developmental Delay and Intellectual Disabilities-A Narrative Review.
Mary Hsin-Ju Ko et al. Children (Basel, Switzerland) 2023 10(3)
Similar articles in PubMed
Designing an international survey for organisations serving people with Down syndrome.
Kats Daniel J et al. Journal of applied research in intellectual disabilities : JARID 2023
Similar articles in PubMed
Indicators of health in Down syndrome: A virtual focus group study with patients and their parents.
Santoro Stephanie L et al. Journal of applied research in intellectual disabilities : JARID 2023
Similar articles in PubMed
Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome.
McGinn Daniel E et al. Genes 2022 13(10)
Similar articles in PubMed
Biological, Behavioral, and Ethical Considerations of Prader-Willi Syndrome: A Primer for Behavior Analysts.
Kennedy Danielle et al. Behavior analysis in practice 2022 15(2) 562-570
Similar articles in PubMed
A Study of the Genomic Variations Associated with Autistic Spectrum Disorders in a Russian Cohort of Patients Using Whole-Exome Sequencing.
Gibitova Ekaterina A et al. Genes 2022 13(5)
Similar articles in PubMed
Fragile X premutation carrier screening in Pakistani preconception women in primary care consultation.
Meraj Neelam et al. BMC women's health 2022 22(1) 57
Similar articles in PubMed
The opinions and experiences of people with intellectual disability regarding genetic testing and genetic medicine: A systematic review.
Strnadová Iva et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021
Similar articles in PubMed
Frequency of carriers for rare recessive Mendelian diseases in a Brazilian cohort of 320 patients.
Quaio Caio Robledo D'Angioli Costa et al. American journal of medical genetics. Part C, Seminars in medical genetics 2021
Similar articles in PubMed
[Experience and lessons on guiding and governing clinical applications of chromosome microarray analysis in the United States].
Xie Xiaolei et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 38(5) 419-424
Similar articles in PubMed
The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects.
Fridman Hila et al. American journal of human genetics 2021
Similar articles in PubMed
COVID-19 infection and outcomes in a population-based cohort of 17,173 adults with intellectual disabilities compared with the general population
A Henderson et al, MEDRXIV, February 9, 2021
Next-generation sequencing for the diagnosis of patients with congenital multiple anomalies and / or intellectual disabilities.
Suga Kenichi et al. The journal of medical investigation : JMI 2020 67(3.4) 246-249
Similar articles in PubMed
Association of polycystic ovary syndrome or anovulatory infertility with offspring psychiatric and mild neurodevelopmental disorders: a Finnish population-based cohort study.
Chen Xinxia et al. Human reproduction (Oxford, England) 2020 Aug
Similar articles in PubMed
An efficient genetic test flow for multiple congenital anomaly and intellectual disability.
Yokoi Takayuki et al. Pediatrics international : official journal of the Japan Pediatric Society 2020 Jan
Similar articles in PubMed
New genetic analysis improves diagnosis of intellectual disability
Karolinska Institute, November 11, 2019
Increase in Developmental Disabilities Among Children in the United States
CDC, September 2019
Education versus screening: the use of capacity to consent tools in psychiatric genomics.
Kong Camillia et al. Journal of medical ethics 2019 Sep
Similar articles in PubMed
Team links gene to children with physical and intellectual disabilities
S Yozwiak, Medical Xpress, August 15, 2019
What do parents expect from a genetic diagnosis of their child with intellectual disability?
Dikow Nicola et al. Journal of applied research in intellectual disabilities : JARID 2019 Apr
Similar articles in PubMed
Using Bayesian methodology to explore the profile of mental health and well-being in 646 mothers of children with 13 rare genetic syndromes in relation to mothers of children with autism.
Adams Dawn et al. Orphanet journal of rare diseases 2018 Oct 13(1) 185
Similar articles in PubMed
Family Genetics Key to Severity of Autism and Other Neurodevelopmental Disorders
GEN News Highlights, September 2018
[FROM GENETICS OF FRAGILE X SYNDROME TO DEVELOPMENT OF TARGETED AND PERSONALIZED DRUG THERAPY].
Gabis Lidia V et al. Harefuah 2018 Aug 157(8) 529-533
Similar articles in PubMed
'We would have missed out so much had we terminated': What fathers of a child with Down syndrome think about current non-invasive prenatal testing for Down syndrome.
How Bethea et al. Journal of intellectual disabilities : JOID 2018 Jan 1744629518787606
Similar articles in PubMed
Marked yield of re-evaluating phenotype and exome/target sequencing data in 33 individuals with intellectual disabilities.
Xiao Bing et al. American journal of medical genetics. Part A 2017 Nov
Similar articles in PubMed
Genetic testing in intellectual disability psychiatry: Opinions and practices of UK child and intellectual disability psychiatrists.
Wolfe Kate et al. Journal of applied research in intellectual disabilities : JARID 2017 Aug
Similar articles in PubMed
File Formats Help:
How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?
Adobe PDF file
Microsoft PowerPoint file
Microsoft Word file
Microsoft Excel file
Audio/Video file
Apple Quicktime file
RealPlayer file
Text file
Zip Archive file
SAS file
ePub file
Page last reviewed:
Feb 1, 2024
Page last updated:
May 21, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
TOP