Obsessive‐compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome

Doron Gothelf, Gadi Presburger, Ada H. Zohar, +12

American Journal of Medical Genetics Part B Neuropsychiatric Genetics

Neurogenetic Microdeletion SyndromesPsychological Co-morbiditiesPsychiatryObsessive‐compulsive DisorderEarly-onset Ocd +10

Chromosomal aberrations and gene expression profiles in non-small cell lung cancer

Elinor Dehan, Amir Ben‐Dor, Wei‐Yu Liao, +14

Lung Cancer

ChromatinOncologyTumor HeterogeneityMedicineGenetics +9

Detection of chromosomal aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization

Michal Daniely, Ayala Aviram‐Goldring, Gad Barkai, +1

Human Reproduction

FertilityCytogeneticsGeneticsComparative Genomic HybridizationReproductive Health +16

Sperm chromosome analysis and outcome of IVF in patients with non-mosaic Klinefelter’s syndrome

Jacob Levron, Ayala Aviram‐Goldring, Igal Madgar, +3

Fertility and Sterility

InfertilityAndrologyFertilityCytogeneticsReproductive Health +10

Sperm chromosome abnormalities in men with severe male factor infertility who are undergoing in vitro fertilization with intracytoplasmic sperm injection

Jacob Levron, Ayala Aviram‐Goldring, Igal Madgar, +3

Fertility and Sterility

InfertilityUrologyMale FertilityFertilityAndrology +12

Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome

Doron Gothelf, Elena Michaelovsky, Amos Frisch, +10

The International Journal of Neuropsychopharmacology

Screening of human pluripotent stem cells using CGH and FISH reveals low-grade mosaic aneuploidy and a recurrent amplification of chromosome 1q

Michal Dekel-Naftali, Ayala Aviram‐Goldring, Talia Litmanovitch, +9

European Journal of Human Genetics

Chromosome 1QChromatinRecurrent AmplificationInduced Pluripotent Stem CellCytogenetics +10

Deletion patterns of the STS gene and flanking sequences in Israeli X-linked ichthyosis patients and carriers: analysis by polymerase chain reaction and fluorescence in situ hybridization techniques

Ayala Aviram‐Goldring, Boleslav Goldman, Irit Netanelov-Shapira, +5

International Journal of Dermatology

Congenital diaphragmatic hernia in a family segregating a reciprocal translocation t(5;15)(p15.3;q24)

Ayala Aviram‐Goldring, Michal Daniely, Moshe Frydman, +3

American Journal of Medical Genetics

Developmental AnomalyDistal DeletionDevelopmental BiologyHernia SurgeryCongenital Diaphragmatic Hernia +9

Detection of numerical chromosome aberrations by comparative genomic hybridization

Michal Daniely, Gad Barkai, Boleslaw Goldman, +1

Prenatal Diagnosis

CytogeneticsGeneticsGynecologyPathologyGenomics +16