Florence Fellmann

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2

Robin Walters, Sébastien Jacquemont, Armand Valsesia et al. · Nature · 2010 · 554 citations · Full text

Obesity, Metabolic Syndrome, Childhood Obesity +9

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey et al. · Nature · 2011 · 474 citations · Full text

Gene Dosage, Genetics, Human Polymorphism +8

Whole-genome sequencing in health care

Carla van El, Martina C. Cornel, Pascal Borry et al. · European Journal of Human Genetics · 2013 · 374 citations · Full text

Sequencing, Next-generation Sequencing, Genomics +4

Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.

Carla van El, Martina C. Cornel, Pascal Borry et al. · PubMed · 2013 · 356 citations · Full text

Whole-genome Sequencing, Sequencing, Medicine +7

SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years

Michito Namekawa, Isabelle Nelson, Sylvie Forlani et al. · Neurology · 2006 · 119 citations