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Colin L. Stewart, Petr Kašpar, Lisa J. Brunet, +4

Nature

OocyteDevelopmental BiologyFertilityBlastocyst ImplantationReproductive Health +5

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay

Rachel D. Burnside, Romela Pasion, Fady M. Mikhail, +14

Human Genetics

Neurodevelopmental DisordersMolecular NeuroscienceProximal 15Q11.2Genetic DisorderGenetics +9

Stem Cells from Primordial Germ Cells Can Reenter the Germ Line

Colin L. Stewart, Inder Gadi, Harshida Bhatt

Developmental Biology

Germ Cell BiologyEmbryonic Stem CellInduced Pluripotent Stem CellDevelopmental BiologyGerm Cell +12

[49] Derivation of embryonic stem cell lines

Susan J. Abbondanzo, Inder Gadi, Colin L. Stewart

Methods in enzymology on CD-ROM/Methods in enzymology

Embryonic Stem CellDevelopmental BiologyCell SpecializationMedicineMorphogenesis +6

UPD detection using homozygosity profiling with a SNP genotyping microarray

Peter Papenhausen, Stuart Schwartz, Hiba Risheg, +8

American Journal of Medical Genetics Part A

Single ChromosomeGenetic TestingSingle Nucleotide PolymorphismGeneticsGenomics +18

Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: Implications for genetic imprinting

Jeff Mann, Inder Gadi, Margaret L. Harbison, +2

Cell

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Gene amplification: an example of accelerated evolution in tumorigenic cells.

Ruth Sager, Inder Gadi, Len Stephens, +1

Proceedings of the National Academy of Sciences

Gene AmplificationPathologyTumor BiologyOncologyTumor Heterogeneity +15

Azacytidine-induced tumorigenesis of CHEF/18 cells: correlated DNA methylation and chromosome changes.

Janie J. Harrison, Anthony Anisowicz, Inder Gadi, +2

Proceedings of the National Academy of Sciences

Nontumorigenic Stable DiploidsEpigenetic ChangeGeneticsDna MethylationCell Proliferation +21

Mosaic paternal genome‐wide uniparental isodisomy with down syndrome

Diana Darcy, Paldeep S. Atwal, Cathy Angell, +2

American Journal of Medical Genetics Part A

Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype

Rachel D. Burnside, John Pappas, Stephanie Sacharow, +12

American Journal of Medical Genetics Part A