M. Watson

Genetics in Medicine · 2006–2016

A researcher in the Science corpus: 6 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Papers from M. Watson's perspective

Ordered by how strongly the researchers M. Watson trusts endorse each paper. Same corpus, a different order for every researcher.

  1. Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
  2. Global variation in copy number in the human genome (Nature)
  3. Procedure‐related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta‐analysis (Ultrasound in Obstetrics and Gynecology)
  4. Origins and functional impact of copy number variation in the human genome (Nature)
  5. Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis (New England Journal of Medicine)
  6. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. (American Journal of Human Genetics)
  7. Care of girls and women with Turner syndrome: a guideline of the Turner Syndrome Study Group. (Journal of Clinical Endocrinology and Metabolism)
  8. The epidemiology of autism spectrum disorders. (Annual Review of Public Health)
  9. Guideline for the diagnosis and treatment of celiac disease in children: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. (Journal of Pediatric Gastroenterology and Nutrition - JPGN)
  10. Next-generation sequencing transforms today's biology (Nature Methods)

Their papers