Các bài viết có thể truy cập công khai - Edward D. EsplinTìm hiểu thêm
Không có ở bất kỳ nơi nào: 1
Clinical implications of pathogenic germline variants in small intestine neuroendocrine tumors (SI-NETs)
K Perez, MH Kulke, A Chittenden, C Ukaegbu, K Astone, H Alexander, ...
JCO Precision Oncology 5, 808-816, 2021
Các cơ quan ủy nhiệm: Susan G. Komen
Có tại một số nơi: 33
The human tumor atlas network: charting tumor transitions across space and time at single-cell resolution
O Rozenblatt-Rosen, A Regev, P Oberdoerffer, T Nawy, A Hupalowska, ...
Cell 181 (2), 236-249, 2020
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, Howard …
Single-cell analyses define a continuum of cell state and composition changes in the malignant transformation of polyps to colorectal cancer
WR Becker, SA Nevins, DC Chen, R Chiu, AM Horning, TK Guha, ...
Nature genetics 54 (7), 985-995, 2022
Các cơ quan ủy nhiệm: US National Institutes of Health
Organization of the human intestine at single-cell resolution
JW Hickey, WR Becker, SA Nevins, A Horning, AE Perez, C Zhu, B Zhu, ...
Nature 619 (7970), 572-584, 2023
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, Cancer …
Personalized sequencing and the future of medicine: discovery, diagnosis and defeat of disease
ED Esplin, L Oei, MP Snyder
Pharmacogenomics 15 (14), 1771-1790, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health
Addressing underrepresentation in genomics research through community engagement
AA Lemke, ED Esplin, AJ Goldenberg, C Gonzaga-Jauregui, ...
The American Journal of Human Genetics 109 (9), 1563-1571, 2022
Các cơ quan ủy nhiệm: US National Institutes of Health
Germline genetic testing after cancer diagnosis
AW Kurian, P Abrahamse, A Furgal, KC Ward, AS Hamilton, R Hodan, ...
Jama 330 (1), 43-51, 2023
Các cơ quan ủy nhiệm: US National Institutes of Health, State of Califonia
Returning integrated genomic risk and clinical recommendations: The eMERGE study
JE Linder, A Allworth, HT Bland, PJ Caraballo, RL Chisholm, EW Clayton, ...
Genetics in Medicine 25 (4), 100006, 2023
Các cơ quan ủy nhiệm: US National Institutes of Health
Nine patients with Xp22. 31 microduplication, cognitive deficits, seizures, and talipes anomalies
ED Esplin, B Li, A Slavotinek, A Novelli, A Battaglia, R Clark, C Curry, ...
American Journal of Medical Genetics Part A 164 (8), 2097-2103, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health
Assessment of the diagnostic yield of combined cardiomyopathy and arrhythmia genetic testing
LM Dellefave-Castillo, AL Cirino, TE Callis, ED Esplin, J Garcia, ...
JAMA cardiology 7 (9), 966-974, 2022
Các cơ quan ủy nhiệm: US National Institutes of Health
RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans
E esplin
Am J Hum Genet, 2015
Các cơ quan ủy nhiệm: Canadian Institutes of Health Research, Genome Canada
Developing and optimizing innovative tools to address familial hypercholesterolemia underdiagnosis: identification methods, patient activation, and cascade testing for familial …
G Campbell-Salome, LK Jones, MF Masnick, NA Walton, CD Ahmed, ...
circulation: genomic and precision medicine 14 (1), e003120, 2021
Các cơ quan ủy nhiệm: US National Institutes of Health
Genomic era diagnosis and management of hereditary and sporadic colon cancer
ED Esplin, MP Snyder
World journal of clinical oncology 5 (5), 1036, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health
Clinical impact of pathogenic germline variants in pancreatic cancer: results from a multicenter, prospective, universal genetic testing study
PLS Uson Jr, NJ Samadder, D Riegert-Johnson, L Boardman, MJ Borad, ...
Clinical and translational gastroenterology, e00414, 2021
Các cơ quan ủy nhiệm: US National Institutes of Health
FH variant pathogenicity promotes purine salvage pathway dependence in kidney cancer
BR Wilde, N Chakraborty, N Matulionis, S Hernandez, D Ueno, ME Gee, ...
Cancer discovery 13 (9), 2072-2089, 2023
Các cơ quan ủy nhiệm: US National Institutes of Health
Fumarate hydratase variant prevalence and manifestations among individuals receiving germline testing
E Lu, KE Hatchell, SM Nielsen, ED Esplin, K Ouyang, K Nykamp, ...
Cancer 128 (4), 675-684, 2022
Các cơ quan ủy nhiệm: US National Institutes of Health
Trans-ethnic variation in germline variants of patients with renal cell carcinoma
S Abou Alaiwi, AH Nassar, E Adib, SM Groha, EW Akl, BA McGregor, ...
Cell reports 34 (13), 2021
Các cơ quan ủy nhiệm: US Department of Defense, US National Institutes of Health
Multigene panel testing in individuals with hepatocellular carcinoma identifies pathogenic germline variants
A Mezina, N Philips, Z Bogus, N Erez, R Xiao, R Fan, KM Olthoff, ...
JCO Precision Oncology 5, 988-1000, 2021
Các cơ quan ủy nhiệm: US National Institutes of Health
Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization
C Eno, P Bayrak-Toydemir, L Bean, A Braxton, EC Chao, D El-Khechen, ...
Genetics in Medicine 21 (4), 861-866, 2019
Các cơ quan ủy nhiệm: US National Institutes of Health
High resolution single cell maps reveals distinct cell organization and function across different regions of the human intestine
JW Hickey, WR Becker, SA Nevins, A Horning, AE Perez, R Chiu, ...
BioRxiv, 2021.11. 25.469203, 2021
Các cơ quan ủy nhiệm: US National Institutes of Health, Cancer Research UK
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