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 (47475)
CDC/NIH Web Information Database (32208)
CDC-Authored Genomics and Precision Health Publications Database (6094)
Precision Health Database (63881)
Tier-Classified Guidelines Database (535)
Pathogen Advanced Molecular Detection Database (26916)
All of Us Reports and Publications Database (698)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (227294)
Epigenetic Epidemiology Publications Database (22891)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Heart, Lung, Blood and Sleep Disorders
Last data update: May 18, 2024
. (Total: 63881 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 31 Records)
Next
Query Trace:
Genomic Analyses of Germline and Somatic Variation in High-Grade Serous Ovarian Cancer.
Aaron W Adamson et al. Research square 2023
Similar articles in PubMed
Retrospective evaluation of clinical and molecular data of 148 cases of esophageal atresia.
Ranza Emmanuelle et al. American journal of medical genetics. Part A 2022
Similar articles in PubMed
Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization.
Hol Janna A et al. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2022 JCO2102510
Similar articles in PubMed
Spectrum of Hematological Malignancies, Clonal Evolution and Outcomes in 144 Mayo Clinic Patients with Germline Predisposition Syndromes.
St Martin Emma et al. American journal of hematology 2021
Similar articles in PubMed
Cell and Gene Therapy for Anemia: Hematopoietic Stem Cells and Gene Editing.
Anurogo Dito et al. International journal of molecular sciences 2021 22(12)
Similar articles in PubMed
Monitoring and treatment of MDS in genetically susceptible persons.
Davies Stella M et al. Hematology. American Society of Hematology. Education Program 2019 2019(1) 105-109
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
Could editing the DNA of embryos with CRISPR help save people who are already alive?
A Joseph, StatNews, September 16, 2019
Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia.
Río Paula, et al. Nature medicine 2019 0 0. (9) 1396-1401
Similar articles in PubMed
Current Knowledge and Priorities for Future Research in Late Effects after Hematopoietic Cell Transplantation for Inherited Bone Marrow Failure Syndromes: Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Pediatric Hematopoietic Cell Transplantation.
Dietz Andrew C et al. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation 2017 May 23(5) 726-735
Similar articles in PubMed
PARP Inhibitors Hit the Pancreatic Cancer Scene
D Ternyila, Oncology Nursing News, August 9, 2019
[Genetic analysis of Japanese patients with Fanconi anemia: novel findings].
Mori Minako et al. [Rinsho ketsueki] The Japanese journal of clinical hematology 2019 60(6) 691-701
Similar articles in PubMed
Prospective Comprehensive Genomic Profiling of Primary and Metastatic Prostate Tumors.
Chung Jon H et al. JCO precision oncology 2019 3
Similar articles in PubMed
Toward the precision breast cancer survival prediction utilizing combined whole genome-wide expression and somatic mutation analysis.
Zhang Yifan et al. BMC medical genomics 2018 Nov 11(Suppl 5) 104
Similar articles in PubMed
Acquired and germline predisposition to bone marrow failure: Diagnostic features and clinical implications.
Kallen Michael E et al. Seminars in hematology 2019 56(1) 69-82
Similar articles in PubMed
Targeted RNA-seq successfully identifies normal and pathogenic splicing events in breast/ovarian cancer susceptibility and Lynch syndrome genes.
Brandão Rita D et al. International journal of cancer 2019 Jan
Similar articles in PubMed
Prevalence of nonfounder BRCA1/2 mutations in Ashkenazi Jewish patients presenting for genetic testing at a hereditary breast and ovarian cancer center.
Frey Melissa K et al. Cancer 2018 Nov
Similar articles in PubMed
Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility.
Catucci Irene et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 20(4) 452-457
Similar articles in PubMed
Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia.
Bogliolo Massimo et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 20(4) 458-463
Similar articles in PubMed
Defective DNA repair in hereditary ovarian cancers: Implications for therapy.
Burgess Brian T et al. American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists 2018 Sep
Similar articles in PubMed
Retrospective evaluation of a decision-support algorithm (MIPOGG) for genetic referrals for children with neuroblastic tumors.
Goudie Catherine et al. Pediatric blood & cancer 2018 Aug e27390
Similar articles in PubMed
Old and new tools in the clinical diagnosis of inherited bone marrow failure syndromes.
West Allison H et al. Hematology. American Society of Hematology. Education Program 2017 2017(1) 79-87
Similar articles in PubMed
[Using target next-generation sequencing assay in diagnosing of 46 patients with suspected congenital anemias].
Li Y et al. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2018 May 39(5) 414-419
Similar articles in PubMed
Genetic Testing in a Cohort of Complex Esophageal Atresia.
Beauregard-Lacroix Eliane et al. Molecular syndromology 2017 Aug 8(5) 236-243
Similar articles in PubMed
A strategy for molecular diagnostics of Fanconi anemia in Brazilian patients.
Pilonetto Daniela V et al. Molecular genetics & genomic medicine 2017 Jul 5(4) 360-372
Similar articles in PubMed
Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders.
Walsh Michael F et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2017 Jun 23(11) e23-e31
Similar articles in PubMed
Revisiting the morbid genome of Mendelian disorders.
Abouelhoda Mohamed et al. Genome biology 2016 Nov 17(1) 235
Similar articles in PubMed
Genetic Information-Seeking Behaviors and Knowledge among Family Members and Patients with Inherited Bone Marrow Failure Syndromes.
Hamilton Jada G et al. Journal of genetic counseling 2015 Oct 24(5) 760-70
Similar articles in PubMed
Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC).
DiNardo Courtney D et al. Clinical lymphoma, myeloma & leukemia 2016 Apr
Similar articles in PubMed
Twenty years of the Italian Fanconi Anemia Registry: where we stand and what remains to be learned.
Risitano Antonio M et al. Haematologica 2015 Dec
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 18, 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