Detalhe da pesquisa
1.
A Mesp1-dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors.
Development
; 150(9)2023 05 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36994838
2.
Genetic and Immunohistochemical Profiling of Mammary Hidradenoma and Comparison to Mucoepidermoid Carcinoma.
Mod Pathol
; 36(10): 100270, 2023 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-37422157
3.
ALK Immunoexpression is Specific for Inflammatory Myofibroblastic Tumor Among Vulvovaginal Mesenchymal Neoplasms.
Int J Gynecol Pathol
; 42(1): 1-10, 2023 Jan 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35180768
4.
Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis.
Am J Obstet Gynecol
; 226(1): 128.e1-128.e11, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34331894
5.
Hydra: A mixture modeling framework for subtyping pediatric cancer cohorts using multimodal gene expression signatures.
PLoS Comput Biol
; 16(4): e1007753, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-32275708
6.
Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features.
Ophthalmology
; 127(6): 804-813, 2020 06.
Artigo
Inglês
| MEDLINE | ID: mdl-32139107
7.
Practical roles for molecular diagnostic testing in ovarian adult granulosa cell tumour, Sertoli-Leydig cell tumour, microcystic stromal tumour and their mimics.
Histopathology
; 76(1): 11-24, 2020 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-31846522
8.
NTRK fusion cervical sarcoma: a report of three cases, emphasising morphological and immunohistochemical distinction from other uterine sarcomas, including adenosarcoma.
Histopathology
; 77(1): 100-111, 2020 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-31971278
9.
Identification of high-risk human papillomavirus and Rb/E2F pathway genomic alterations in mutually exclusive subsets of colorectal neuroendocrine carcinoma.
Mod Pathol
; 32(2): 290-305, 2019 02.
Artigo
Inglês
| MEDLINE | ID: mdl-30237525
10.
Genetic ancestry and diagnostic yield of exome sequencing in a diverse population.
NPJ Genom Med
; 9(1): 1, 2024 Jan 03.
Artigo
Inglês
| MEDLINE | ID: mdl-38172272
11.
A disrupted compartment boundary underlies abnormal cardiac patterning and congenital heart defects.
bioRxiv
; 2024 Mar 04.
Artigo
Inglês
| MEDLINE | ID: mdl-38370632
12.
Diagnostic Yield of Exome Sequencing in a Diverse Pediatric and Prenatal Population is not Associated with Genetic Ancestry.
medRxiv
; 2023 May 24.
Artigo
Inglês
| MEDLINE | ID: mdl-37293051
13.
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
NPJ Genom Med
; 8(1): 10, 2023 May 26.
Artigo
Inglês
| MEDLINE | ID: mdl-37236975
14.
Novel SOX10 indel mutations drive schwannomas through impaired transactivation of myelination gene programs.
Neuro Oncol
; 25(12): 2221-2236, 2023 12 08.
Artigo
Inglês
| MEDLINE | ID: mdl-37436963
15.
Expanding the phenotype of males with OFD1 pathogenic variants-a case report and literature review.
Eur J Med Genet
; 65(6): 104496, 2022 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-35398350
16.
Homologous Recombination Deficiency and Ovarian Cancer Treatment Decisions: Practical Implications for Pathologists for Tumor Typing and Reporting.
Surg Pathol Clin
; 15(2): 219-234, 2022 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-35715159
17.
Tumor and Constitutional Sequencing for Neurofibromatosis Type 1.
JCO Precis Oncol
; 6: e2100540, 2022 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35584348
18.
Cytoplasmic Pattern p53 Immunoexpression in Pelvic and Endometrial Carcinomas With TP53 Mutation Involving Nuclear Localization Domains: An Uncommon But Potential Diagnostic Pitfall With Clinical Implications.
Am J Surg Pathol
; 45(11): 1441-1451, 2021 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33899789
19.
Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart Disease.
Dev Cell
; 56(3): 292-309.e9, 2021 02 08.
Artigo
Inglês
| MEDLINE | ID: mdl-33321106
20.
A novel reporter allele for monitoring Dll4 expression within the embryonic and adult mouse.
Biol Open
; 7(3)2018 Mar 12.
Artigo
Inglês
| MEDLINE | ID: mdl-29437553