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Stephanie LaHaye
Stephanie LaHaye
Tempus Labs, Inc.
在 tempus.com 的电子邮件经过验证 - 首页
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Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease
K Bosse, CP Hans, N Zhao, SN Koenig, N Huang, A Guggilam, S LaHaye, ...
Journal of molecular and cellular cardiology 60, 27-35, 2013
1822013
Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve
EM Bonachea, SW Chang, G Zender, S LaHaye, S Fitzgerald-Butt, ...
Pediatric research 76 (2), 211-216, 2014
952014
Genetics of valvular heart disease
S LaHaye, J Lincoln, V Garg
Current cardiology reports 16, 1-9, 2014
922014
Utilization of whole exome sequencing to identify causative mutations in familial congenital heart disease
S LaHaye, D Corsmeier, M Basu, JL Bowman, S Fitzgerald-Butt, G Zender, ...
Circulation: Cardiovascular Genetics 9 (4), 320-329, 2016
872016
Epigenetic mechanisms underlying maternal diabetes-associated risk of congenital heart disease
M Basu, JY Zhu, S LaHaye, U Majumdar, K Jiao, Z Han, V Garg
JCI insight 2 (20), 2017
702017
Notch1 haploinsufficiency causes ascending aortic aneurysms in mice
SN Koenig, S LaHaye, JD Feller, P Rowland, KN Hor, AJ Trask, ...
JCI insight 2 (21), 2017
532017
Detection of brain somatic variation in epilepsy‐associated developmental lesions
TA Bedrosian, KE Miller, OE Grischow, KM Schieffer, S LaHaye, H Yoon, ...
Epilepsia 63 (8), 1981-1997, 2022
392022
Evidence of pioneer factor activity of an oncogenic fusion transcription factor
BD Sunkel, M Wang, S LaHaye, BJ Kelly, JR Fitch, FG Barr, P White, ...
IScience 24 (8), 2021
202021
YAP1-FAM118B fusion defines a rare subset of childhood and young adulthood meningiomas
KM Schieffer, V Agarwal, S LaHaye, KE Miller, DC Koboldt, T Lichtenberg, ...
The American Journal of Surgical Pathology 45 (3), 329-340, 2021
192021
Developmental origins for semilunar valve stenosis identified in mice harboring congenital heart disease-associated GATA4 mutation
S LaHaye, U Majumdar, J Yasuhara, SN Koenig, A Matos-Nieves, ...
Disease models & mechanisms 12 (6), dmm036764, 2019
182019
Discovery of clinically relevant fusions in pediatric cancer
S LaHaye, JR Fitch, KJ Voytovich, AC Herman, BJ Kelly, GE Lammi, ...
BMC genomics 22, 1-16, 2021
172021
KPT-330 prevents aortic valve calcification via a novel C/EBPβ signaling pathway
P Dutta, KM Kodigepalli, S LaHaye, JW Thompson, S Rains, C Nagel, ...
Circulation research 128 (9), 1300-1316, 2021
152021
High early death rates, treatment resistance, and short survival of Black adolescents and young adults with AML
KT Larkin, D Nicolet, BJ Kelly, K Mrózek, S LaHaye, KE Miller, S Wijeratne, ...
Blood advances 6 (19), 5570-5581, 2022
132022
Gastroblastoma with a novel EWSR1‐CTBP1 fusion presenting in adolescence
SC Koo, S LaHaye, BP Kovari, KM Schieffer, MA Ranalli, JH Aldrink, ...
Genes, Chromosomes and Cancer 60 (9), 640-646, 2021
132021
Postnatal and adult aortic heart valves have distinctive transcriptional profiles associated with valve tissue growth and maintenance respectively
E Nordquist, S LaHaye, C Nagel, J Lincoln
Frontiers in cardiovascular medicine 5, 30, 2018
132018
Novel morphologic findings in PLAG1‐rearranged soft tissue tumors
SJ Logan, KM Schieffer, MR Conces, E Stonerock, AR Miller, J Fitch, ...
Genes, Chromosomes and Cancer 60 (8), 577-585, 2021
112021
Clinically aggressive pediatric spinal ependymoma with novel MYC amplification demonstrates molecular and histopathologic similarity to newly described MYCN-amplified spinal …
M Shatara, KM Schieffer, D Klawinski, DL Thomas, CR Pierson, ...
Acta neuropathologica communications 9 (1), 192, 2021
92021
Evidence of pioneer factor activity of an oncogenic fusion transcription factor. iScience 24
BD Sunkel, M Wang, S LaHaye, BJ Kelly, JR Fitch, FG Barr, P White, ...
72021
Tgfβ1-cthrc1 signaling plays an important role in the short-term reparative response to heart valve endothelial injury
EM Nordquist, P Dutta, KM Kodigepalli, C Mattern, MR McDermott, ...
Arteriosclerosis, thrombosis, and vascular biology 41 (12), 2923-2942, 2021
62021
Molecular classification of a complex structural rearrangement of the RB1 locus in an infant with sporadic, isolated, intracranial, sellar region retinoblastoma
KM Schieffer, AZ Feldman, EA Kautto, S McGrath, AR Miller, ...
Acta neuropathologica communications 9, 1-11, 2021
62021
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