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You searched for: Author/Creator Reymond, Alexandre

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1. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders. Issue 10 (10th October 2012)

2. A mitochondria-specific mutational signature of aging: increased rate of A > G substitutions on the heavy strand. Issue 18 (21st September 2022)

3. Alpha Satellite Insertion Close to an Ancestral Centromeric Region. (31st August 2021)

4. Copy Number Variations and Cognitive Phenotypes in Unselected Populations. Issue 9 (September 2015)

7. Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs. Issue 1 (21st February 2021)

8. GENCODE reference annotation for the human and mouse genomes. Issue Volume 47:Issue D1(2019) (24th October 2018)

9. Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria. Issue 4 (6th September 2022)

10. Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics. Issue 1 (December 2016)