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 (47395)
CDC/NIH Web Information Database (32189)
CDC-Authored Genomics and Precision Health Publications Database (6062)
Precision Health Database (63767)
Tier-Classified Guidelines Database (534)
Pathogen Advanced Molecular Detection Database (26823)
All of Us Reports and Publications Database (679)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (226753)
Epigenetic Epidemiology Publications Database (22811)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 02, 2024
. (Total: 63767 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 43 Records)
Next
Query Trace:
Secondary (additional) findings from the 100,000 Genomes Project: disease manifestation, healthcare outcomes and costs of disclosure.
Joshua Nolan et al. Genet Med 2023 101051
Similar articles in PubMed
Lived experiences of undergoing regular tumor screening in patients with multiple endocrine neoplasia types 1 and 2 (MEN1/MEN2).
Mirthe Jasmijn Klein Haneveld et al. J Genet Couns 2023
Similar articles in PubMed
Mainstreaming of genomics in oncology: a nationwide survey of the genomics training needs of UK oncologists.
Rippie K Tutika et al. Clinical medicine (London, England) 2023 23(1) 9-15
Similar articles in PubMed
Multiple Endocrine Neoplasia Type 2 (MEN2) and RET Specific Modifications of the ACMG/AMP Variant Classification Guidelines and Impact on the MEN2 RET Database.
Margraf Rebecca L et al. Human mutation 2022
Similar articles in PubMed
Genetics of Pancreatic Neuroendocrine Tumors.
Mohindroo Chirayu et al. Hematology/oncology clinics of North America 2022
Similar articles in PubMed
Cancer predisposing syndrome: a retrospective cohort analysis in a pediatric and multidisciplinary genetic cancer counseling unit.
Escudero Adela et al. International journal of clinical oncology 2022
Similar articles in PubMed
A review of inherited cancer susceptibility syndromes.
Brown Gina R et al. JAAPA : official journal of the American Academy of Physician Assistants 2020 Dec 33(12) 10-16
Similar articles in PubMed
A review of inherited cancer susceptibility syndromes.
Brown Gina R et al. JAAPA : official journal of the American Academy of Physician Assistants 2020 Nov
Similar articles in PubMed
Outcome of Clinical Genetic Testing in Patients with Features Suggestive for Hereditary Predisposition to PTH-Mediated Hypercalcemia.
Khairi Shafaq et al. Hormones & cancer 2020 Aug
Similar articles in PubMed
Inherited syndromes involving pancreatic neuroendocrine tumors.
Geurts Jennifer L et al. Journal of gastrointestinal oncology 2020 Jun 11(3) 559-566
Similar articles in PubMed
[Challenges of screening germline predispositions in children].
Manabe Atsushi et al. [Rinsho ketsueki] The Japanese journal of clinical hematology 2020 61(6) 682-686
Similar articles in PubMed
Hereditary Parathyroid Disease: Sometimes Pathologists Do Not Know What They Are Missing.
Turchini John et al. Endocrine pathology 2020 May
Similar articles in PubMed
Genetic testing for hereditary hyperparathyroidism and familial hypocalciuric hypercalcaemia in a large UK cohort.
Mariathasan S et al. Clinical endocrinology 2020 May
Similar articles in PubMed
Health-related quality of life in patients with Multiple Endocrine Neoplasia type 1.
van Leeuwaarde Rachel S et al. Neuroendocrinology 2020 May
Similar articles in PubMed
Proposition of adjustments to the ACMG-AMP framework for the interpretation of MEN1 missense variants.
Romanet Pauline et al. Human mutation 2019 40(6) 661-674
Similar articles in PubMed
Challenges and opportunities in genetic counseling for hereditary endocrine neoplasia syndromes.
Brock Pamela L et al. Endocrine-related cancer 2020 Feb
Similar articles in PubMed
A primer on the genetics of medullary thyroid cancer.
Larouche V et al. Current oncology (Toronto, Ont.) 2019 Dec 26(6) 389-394
Similar articles in PubMed
Complicated Case Presentation: Management of Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1.
Mulvey Claire K et al. Pancreas 2017 46(3) 416-426
Similar articles in PubMed
Local Coverage Determination (LCD): Biomarker Testing for Neuroendocrine Tumors/Neoplasms (L37851)
The U.S. Centers for Medicare & Medicaid Services
CLINGEN Actionability Report for Multiple Endocrine Neoplasia Type IIB - RET
ClinGen Actionability Working Group
CLINGEN Actionability Report for Multiple Endocrine Neoplasia Type I - MEN1
ClinGen Actionability Working Group
CLINGEN Actionability Report for Multiple Endocrine Neoplasia IIA, Familial Medullary Thyroid Cancer - RET
ClinGen Actionability Working Group
ONCOGENE PANEL SEQUENCING ANALYSIS IDENTIFIES CANDIDATE ACTIONABLE GENES IN ADVANCED WELL-DIFFERENTIATED GASTROENTEROPANCREATIC NEUROENDOCRINE TUMORS.
Tirosh Amit et al. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2019 Jun 25(6) 580-588
Similar articles in PubMed
Long-Term Outcomes and Aggressiveness of Hereditary Medullary Thyroid Carcinoma: 40 Years of Experience at One Center.
Raue Friedhelm et al. The Journal of clinical endocrinology and metabolism 2019 May
Similar articles in PubMed
Clinical utility of genetic diagnosis for sporadic and hereditary medullary thyroid carcinoma.
Elisei Rossella et al. Annales d'endocrinologie 2019 Apr
Similar articles in PubMed
Long-term follow-up of RET Y791F carriers in Denmark 1994-2017: A National Cohort Study.
Høxbroe Michaelsen Sanne et al. Journal of surgical oncology 2019 May 119(6) 687-693
Similar articles in PubMed
Multiple endocrine neoplasia type 1: extensive analysis of a large database of Florentine patients.
Marini Francesca et al. Orphanet journal of rare diseases 2018 13(1) 205
Similar articles in PubMed
Patient quality of life and prognosis in multiple endocrine neoplasia type 2.
Grey Joanna et al. Endocrine-related cancer 2018 25(2) T69-T77
Similar articles in PubMed
Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study.
Castinetti Frederic et al. The lancet. Diabetes & endocrinology 2019 Jan
Similar articles in PubMed
'Quality in, quality out', a stepwise approach to EBM for rare diseases promoted by MEN1.
van Beek Dirk-Jan et al. Endocrine connections 2018 Sep
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 02, 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