Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II

Neil E. Lamb, Sallie B. Freeman, Amanda Savage-Austin, +12

Nature Genetics

BiologyChromatinChromosome DynamicsCell DivisionMedicine +12

Identification of Krüppel-like factor 4 as a potential tumor suppressor gene in colorectal cancer

Weidong Zhao, Irfan M. Hisamuddin, Mandayam O. Nandan, +3

Oncogene

Krüppel-like Factor 4Tumor BiologyMedicineColorectal CancerPathology +8

Genomic diagnosis for children with intellectual disability and/or developmental delay

Kevin M. Bowling, Michelle L. Thompson, Michelle D. Amaral, +18

Genome Medicine

Recombination rate and reproductive success in humans

Augustine Kong, John Barnard, Daníel F. Guðbjartsson, +10

Nature Genetics

Reproduction ResponseInfertilityReproductive SuccessFertilityMedicine +8

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21

Neil E. Lamb

Human Molecular Genetics

CytogeneticsGeneticsPathologyMeiosis IiMolecular Genetics +21

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

Robert C. Green, Katrina A.B. Goddard, Gail P. Jarvik, +271

The American Journal of Human Genetics

EpidemiologySequencingMedicineNext-generation SequencingGenomics +5

Association between Maternal Age and Meiotic Recombination for Trisomy 21

Neil E. Lamb, Kai Yu, John R. Shaffer, +2

The American Journal of Human Genetics

Maternal AgeGeneticsReproductive HealthGenetic EpidemiologyGynecology +9

What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report

Belén Hurlé, Toby Citrin, Jean Jenkins, +4

Genetics in Medicine

BiologyGeneticsGenome AnalysisGenomicsGenomic Selection +2

LKB1 mutation in large cell carcinoma of the lung

Diansheng Zhong, Lizheng Guo, Itziar de Aguirre, +6

Lung Cancer

Tumor BiologyPathologyBronchial NeoplasmCancer GeneticsMedicine +3

Systematic reanalysis of genomic data improves quality of variant interpretation

Susan M. Hiatt, Michelle D. Amaral, Kevin M. Bowling, +17

Clinical Genetics