Recombinant Vitronectin Is a Functionally Defined Substrate That Supports Human Embryonic Stem Cell Self-Renewal via αVβ5 Integrin

Stefan Braam, Laura Zeinstra, Sandy H.M. Litjens, +9

Stem Cells

Ecm RequirementsCell AdhesionRecombinant VitronectinEcm ProductionStem Cell Biology +16

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Claire Redin, Harrison Brand, Ryan L. Collins, +146

Nature Genetics

Human Congenital AnomaliesDevelopmental AnomalyDevelopmental BiologyCytogeneticsGenomic Landscape +6

Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands

Ron Hochstenbach, Ellen van Binsbergen, J.J.M. Engelen, +7

European Journal of Medical Genetics

Developmental AnomalyEarly DiagnosisWorkflow ConsequencesCognitive DevelopmentPediatrics +7

TGF-β1 induces efficient differentiation of human cardiomyocyte progenitor cells into functional cardiomyocytes in vitro

Marie‐José Goumans, Teun P. de Boer, Anke M. Smits, +14

Stem Cell Research

Regenerative MedicineCardiomyopathyDevelopmental BiologyMedicineCardiac Progenitor Cells +8

Constitutional Chromothripsis Rearrangements Involve Clustered Double-Stranded DNA Breaks and Nonhomologous Repair Mechanisms

Wigard P. Kloosterman, Masoumeh Tavakoli‐Yaraki, Markus J. van Roosmalen, +19

Cell Reports

Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism

Bert van der Zwaag, Lude Franke, Martin Poot, +20

PLoS ONE

GeneticsMolecular BiologyGene CharacterizationDisease Gene IdentificationGenomics +16

Selective chromosome analysis in couples with two or more miscarriages: case-control study

Maureen Franssen, Johanna C. Korevaar, N. J. Leschot, +8

BMJ

A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome

Deniz Kanber, Jacques C. Giltay, Dagmar Wieczorek, +6

European Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsClinical GeneticsGenetic Epidemiology +12

Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring

Mirjam S. de Pagter, Markus J. van Roosmalen, Annette F. Baas, +8

The American Journal of Human Genetics

Severe Congenital AbnormalitiesChromatinDevelopmental AnomalyDevelopmental BiologyGenetic Disorder +11

A co‐segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder

Bert van der Zwaag, Wouter Staal, Ron Hochstenbach, +14

American Journal of Medical Genetics Part B Neuropsychiatric Genetics

NeurogenomicsGeneticsRisk GenesMolecular GeneticsDisease Gene Identification +15