Matthew G. Sampson
Matthew G. Sampson
Boston Children's Hospital
Verified email at - Homepage
Cited by
Cited by
A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
Tissue transcriptome-driven identification of epidermal growth factor as a chronic kidney disease biomarker
W Ju, V Nair, S Smith, L Zhu, K Shedden, PXK Song, LH Mariani, ...
Science translational medicine 7 (316), 316ra193-316ra193, 2015
Design of the Nephrotic Syndrome Study Network (NEPTUNE) to evaluate primary glomerular nephropathy by a multidisciplinary approach
CA Gadegbeku, DS Gipson, LB Holzman, AO Ojo, PXK Song, L Barisoni, ...
Kidney international 83 (4), 749-756, 2013
Copy-number disorders are a common cause of congenital kidney malformations
S Sanna-Cherchi, K Kiryluk, KE Burgess, M Bodria, MG Sampson, ...
The American Journal of Human Genetics 91 (6), 987-997, 2012
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
M Verbitsky, R Westland, A Perez, K Kiryluk, Q Liu, P Krithivasan, ...
Nature genetics 51 (1), 117-127, 2019
An eQTL landscape of kidney tissue in human nephrotic syndrome
CE Gillies, R Putler, R Menon, E Otto, K Yasutake, V Nair, P Hoover, ...
The American Journal of Human Genetics 103 (2), 232-244, 2018
Genetic drivers of kidney defects in the DiGeorge syndrome
E Lopez-Rivera, YP Liu, M Verbitsky, BR Anderson, VP Capone, EA Otto, ...
New England Journal of Medicine 376 (8), 742-754, 2017
Discovery of autoantibodies targeting nephrin in minimal change disease supports a novel autoimmune etiology
AJB Watts, KH Keller, G Lerner, I Rosales, AB Collins, M Sekulic, ...
Journal of the American Society of Nephrology 33 (1), 238-252, 2022
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
J Xie, L Liu, N Mladkova, Y Li, H Ren, W Wang, Z Cui, L Lin, X Hu, X Yu, ...
Nature communications 11 (1), 1600, 2020
Integrative genomics identifies novel associations with APOL1 risk genotypes in black NEPTUNE subjects
MG Sampson, CC Robertson, S Martini, LH Mariani, KV Lemley, ...
Journal of the American Society of Nephrology 27 (3), 814-823, 2016
Exome-wide association study identifies GREB1L mutations in congenital kidney malformations
S Sanna-Cherchi, K Khan, R Westland, P Krithivasan, L Fievet, ...
The American Journal of Human Genetics 101 (5), 789-802, 2017
Genomic Mismatch at LIMS1 Locus and Kidney Allograft Rejection
NJ Steers, Y Li, Z Drace, JA D’Addario, C Fischman, L Liu, K Xu, YJ Na, ...
New England Journal of Medicine 380 (20), 1918-1928, 2019
Appetitive traits associated with higher and lower body mass index: evaluating the validity of the adult eating behaviour questionnaire in an Australian sample
KM Mallan, A Fildes, X de la Piedad Garcia, J Drzezdzon, M Sampson, ...
International Journal of Behavioral Nutrition and Physical Activity 14, 1-8, 2017
CureGN study rationale, design, and methods: establishing a large prospective observational study of glomerular disease
LH Mariani, AS Bomback, PA Canetta, MF Flessner, M Helmuth, ...
American journal of kidney diseases 73 (2), 218-229, 2019
Transethnic, genome-wide analysis reveals immune-related risk alleles and phenotypic correlates in pediatric steroid-sensitive nephrotic syndrome
H Debiec, C Dossier, E Letouzé, CE Gillies, M Vivarelli, RK Putler, E Ars, ...
Journal of the American Society of Nephrology 29 (7), 2000-2013, 2018
APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic …
DK Ng, CC Robertson, RP Woroniecki, S Limou, CE Gillies, KJ Reidy, ...
Nephrology Dialysis Transplantation 32 (6), 983-990, 2017
A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis
H Yu, M Artomov, S Brähler, MC Stander, G Shamsan, MG Sampson, ...
The Journal of clinical investigation 126 (3), 1067-1078, 2016
Complete remission in the nephrotic syndrome study network
DS Gipson, JP Troost, RA Lafayette, MA Hladunewich, H Trachtman, ...
Clinical Journal of the American Society of Nephrology 11 (1), 81-89, 2016
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis
SE Graham, JB Nielsen, M Zawistowski, W Zhou, LG Fritsche, ...
Nature communications 10 (1), 1847, 2019
Evidence for a recurrent microdeletion at chromosome 16p11. 2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease
MG Sampson, CR Coughlin, P Kaplan, LK Conlin, KEC Meyers, ...
American Journal of Medical Genetics Part A 152 (10), 2618-2622, 2010
The system can't perform the operation now. Try again later.
Articles 1–20