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European Journal of Human Genetics : EJHG|December 15, 2010
Phenotypic manifestations of copy number variation in chromosome 16p13.11Sandesh C Sreenath Nagamani, Ayelet Erez, Patricia Bader, et al.
Molecular Metabolism|September 20, 2013
Differential colonization with segmented filamentous bacteria and Lactobacillus murinus do not drive divergent development of diet-induced obesity in C57BL/6 miceIsaac T W Harley, Daniel A Giles, Paul T Pfluger, et al.
Annals of Hematology|May 17, 2023
Therapy results in pediatric Hodgkin lymphoma - does less mean better? Experience from a single children's oncology centerJoanna Stankiewicz, Andrzej Kołtan, Ewa Demidowicz, et al.
Developmental Cell|October 9, 2024
Sex-biased human thymic architecture guides T cell development through spatially defined nichesLaura N Stankiewicz, Kevin Salim, Emily A Flaschner, et al.
The Journal of Urology|August 8, 2019
Noninvasive Detection of Clinically Significant Prostate Cancer Using Circulating Tumor CellsLei Xu, Xueying Mao, Alistair Grey, et al.
Genome Medicine|July 28, 2019
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencingYe Cao, Mari J Tokita, Edward S Chen, et al.
Pediatric Neurology|June 27, 2024
Epilepsy as a Novel Phenotype of BPTF-Related DisordersAlessandro Ferretti, Margherita Furlan, Kevin E Glinton, et al.
Plos Genetics|November 24, 2016
Mechanisms for Complex Chromosomal InsertionsShen Gu, Przemyslaw Szafranski, Zeynep Coban Akdemir, et al.
Human Molecular Genetics|March 28, 2009
Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switchingClaudia M B Carvalho, Feng Zhang, Pengfei Liu, et al.
The Journal of Molecular Diagnostics : JMD|February 10, 2020
Highly Sensitive Blocker Displacement Amplification and Droplet Digital PCR Reveal Low-Level Parental FOXF1 Somatic Mosaicism in Families with Alveolar Capillary Dysplasia with Misalignment of Pulmonary VeinsJustyna A Karolak, Qian Liu, Nina G Xie, et al.
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