Detalhe da pesquisa
1.
X chromosome reactivation dynamics reveal stages of reprogramming to pluripotency.
Cell
; 159(7): 1681-97, 2014 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25525883
2.
A genetic history of the pre-contact Caribbean.
Nature
; 590(7844): 103-110, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33361817
3.
Comparative Clinicopathologic and Genomic Analysis of Hepatocellular Neoplasm, Not Otherwise Specified, and Hepatoblastoma.
Mod Pathol
; 37(2): 100385, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37992967
4.
Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group.
Genet Med
; 26(3): 101036, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38054408
5.
Benign Lobular Inner Nuclear Layer Proliferations of the Retina Associated with Congenital Hypertrophy of the Retinal Pigment Epithelium.
Ophthalmology
; 130(3): 265-273, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36270406
6.
Hidden cargo: The impact of historical shipping trade on the recent-past and contemporary non-native flora of northeastern United States.
Am J Bot
; 110(9): e16224, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37551431
7.
Clinical Integration of a Highly Accurate Polymerase Chain Reaction Point-of-Care Test Can Inform Immediate Treatment Decisions for Chlamydia, Gonorrhea, and Trichomonas.
Sex Transm Dis
; 49(4): 262-267, 2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34813579
8.
High prevalence of deleterious mutations in concomitant nonsyndromic cleft and outflow tract heart defects.
Am J Med Genet A
; 188(7): 2082-2095, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35385219
9.
PLAG1 Immunohistochemical Staining Is a Surrogate Marker for PLAG1 Fusions in Lipoblastomas.
Pediatr Dev Pathol
; 25(2): 134-140, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34601996
10.
Expanding the spectrum of dicer1-associated sarcomas.
Mod Pathol
; 33(1): 164-174, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31537896
11.
Considerations for clinical curation, classification, and reporting of low-penetrance and low effect size variants associated with disease risk.
Genet Med
; 21(12): 2765-2773, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31147632
12.
Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework.
Genet Med
; 21(7): 1507-1516, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30523343
13.
Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical next-generation sequencing.
Genet Med
; 18(12): 1282-1289, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27228465
14.
Peripheral Restricted Diffusion: A Common Appearance of Hepatic Abscesses.
J Comput Assist Tomogr
; 39(6): 890-5, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26466106
15.
Transcriptome Sequencing Allows Comprehensive Genomic Characterization of Pediatric B-Acute Lymphoblastic Leukemia in an Academic Clinical Laboratory.
J Mol Diagn
; 26(1): 49-60, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37981088
16.
Histone H3 trimethylation on lysine 27 immunostaining pattern in DICER1-associated tumors.
Transl Pediatr
; 13(4): 624-633, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38715664
17.
Evaluation of an injectable monthly extended-release buprenorphine program in a low-barrier specialty addiction medicine clinic.
J Subst Use Addict Treat
; 156: 209183, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37879433
18.
Pediatric Sertoli-Leydig Cell Tumors of the Ovary: An Integrated Study of Clinicopathological Features, Pan-cancer-Targeted Next-generation Sequencing and Chromosomal Microarray Analysis From a Single Institution.
Am J Surg Pathol
; 48(2): 194-203, 2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37946548
19.
An Exome Capture-Based RNA-Sequencing Assay for Genome-Wide Identification and Prioritization of Clinically Important Fusions in Pediatric Tumors.
J Mol Diagn
; 26(2): 127-139, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38008288
20.
Significance Associated with Phenotype Score Aids in Variant Prioritization for Exome Sequencing Analysis.
J Mol Diagn
; 26(5): 337-348, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38360210