关注
Pagna Sok
Pagna Sok
在 bcm.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
Association between birth defects and cancer risk among children and adolescents in a population-based assessment of 10 million live births
PJ Lupo, JM Schraw, TA Desrosiers, WN Nembhard, PH Langlois, ...
JAMA oncology 5 (8), 1150-1158, 2019
1372019
Cerebrospinal fluid metabolomic profiles associated with fatigue during treatment for pediatric acute lymphoblastic leukemia
AL Brown, P Sok, O Taylor, JP Woodhouse, MB Bernhardt, KP Raghubar, ...
Journal of pain and symptom management 61 (3), 464-473, 2021
222021
Altered mechanisms of genital development identified through integration of DNA methylation and genomic measures in hypospadias
MA Richard, P Sok, S Canon, WN Nembhard, AL Brown, ...
Scientific Reports 10 (1), 12715, 2020
212020
An updated assessment of 43,110 patients enrolled in the Childhood Cancer Research Network: A Children's Oncology Group report
AL Brown, P Sok, ME Scheurer, KR Rabin, EL Marcotte, DS Hawkins, ...
Cancer 128 (14), 2760-2767, 2022
112022
Utilization of archived neonatal dried blood spots for genome-wide genotyping
P Sok, PJ Lupo, MA Richard, KR Rabin, EA Ehli, NA Kallsen, GE Davies, ...
PLoS One 15 (2), e0229352, 2020
102020
Trends in overall survival among patients treated for sarcoma at a large tertiary cancer center between 1986 and 2014
E Stricker, DR Reed, MB Schabath, P Sok, ME Scheurer, PJ Lupo
Cancers 15 (2), 514, 2023
72023
Evaluation of the sociodemographic, behavioral and clinical influences on complete antiretroviral therapy adherence among HIV-infected adults receiving medical care in Houston …
P Sok, O Mgbere, L Pompeii, EJ Essien
HIV/AIDS-Research and Palliative Care, 539-555, 2021
72021
The role of genetic variation in DGKK on moderate and severe hypospadias
MA Richard, P Sok, S Canon, AL Brown, EC Peckham‐Gregory, ...
Birth defects research 111 (13), 932-937, 2019
72019
Associations between birth defects and childhood and adolescent germ cell tumors according to sex, histologic subtype, and site
JM Schraw, P Sok, TA Desrosiers, AE Janitz, PH Langlois, MA Canfield, ...
Cancer 129 (20), 3300-3308, 2023
42023
Germline genetic variants and pediatric rhabdomyosarcoma outcomes: a report from the Children’s Oncology Group
BA Martin-Giacalone, MA Richard, ME Scheurer, J Khan, P Sok, ...
JNCI: Journal of the National Cancer Institute 115 (6), 733-741, 2023
32023
Exome‐wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify …
P Sok, A Sabo, LM Almli, MM Jenkins, WN Nembhard, AJ Agopian, ...
American Journal of Medical Genetics Part A 191 (6), 1546-1556, 2023
32023
Disparities in relapse among a large multi-ethnic population of children diagnosed with acute lymphoblastic leukemia (ALL): A report from the Reducing Ethnic Disparities in …
P Sok, AL Brown, OA Taylor, MB Bernhardt, JC Bernini, RA Erana, ...
Cancer Research 82 (12_Supplement), 3633-3633, 2022
32022
Genetic susceptibility to cognitive decline following craniospinal irradiation for pediatric central nervous system tumors
AL Brown, P Sok, KP Raghubar, PJ Lupo, MA Richard, AC Morrison, ...
Neuro-oncology 25 (9), 1698-1708, 2023
22023
Epigenome-wide association study of acute lymphoblastic leukemia in children with Down syndrome
S Li, P Sok, K Xu, IS Muskens, N Elliott, SS Myint, P Pandey, HM Hansen, ...
Blood Advances 6 (14), 4132-4136, 2022
12022
Predictors of Art Adherence among HIV-infected Persons Receiving Medical Care in Houston, Texas
P Sok
The University of Texas School of Public Health, 2018
12018
Association of Latino Ethnicity with Cytogenetic Subtype in Pediatric Acute Lymphoblastic Leukemia: A Report from the Reducing Ethnic Disparities in Acute Leukemia Consortium
MD Leon-Camarena, JM Geris, MI Castellanos, O Taylor, ...
Blood 142, 4206, 2023
2023
Differential newborn DNA methylation among individuals with complex congenital heart defects and childhood lymphoma
MA Richard, W Yang, P Sok, M Li, SL Carmichael, J von Behren, ...
Birth Defects Research 114 (20), 1434-1439, 2022
2022
Identification of common germline variants associated with pediatric rhabdomyosarcoma survival: A report from the Children's Oncology Group (COG)
BA Martin-Giacalone, ME Scheurer, J Khan, SJ Chanock, SA Li, M Yeager, ...
Cancer Research 82 (12_Supplement), 683-683, 2022
2022
Exome-Wide Assessment of Isolated Biliary Atresia: Using Child-Parent Trios and a Case-Control Design to Identify Novel Rare Variants
P Sok, A Sabo, LM Almli, MM Jenkins, WN Nembhard, AJ Agopian, ...
BIRTH DEFECTS RESEARCH 114 (9), 405-406, 2022
2022
Epigenome-Wide Association Study of Acute Lymphoblastic Leukemia in Children with Down Syndrome
S Li, P Sok, K Xu, IS Muskens, N Elliott, SS Myint, P Pandey, HM Hansen, ...
Blood 138, 214, 2021
2021
系统目前无法执行此操作,请稍后再试。
文章 1–20