Michail Spiliopoulos

Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia

Michail Spiliopoulos, Francesco Brancati, Eric Powell et al. · The American Journal of Human Genetics · 2011 · 256 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7

MASP1 Mutations in Patients with Facial, Umbilical, Coccygeal, and Auditory Findings of Carnevale, Malpuech, OSA, and Michels Syndromes

Tom Walsh, Hatice Akay, Michail Spiliopoulos et al. · The American Journal of Human Genetics · 2010 · 139 citations · Full text

Developmental Anomaly, Mendelian Disorder, Genetic Disorder +6

De novo ACTG2 mutations cause congenital distended bladder, microcolon, and intestinal hypoperistalsis

Willa Thorson, Oscar Diaz‐Horta, Joseph Foster et al. · Human Genetics · 2013 · 101 citations

Urology, Developmental Biology, Medicine +6

Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome

Kemal O. Yariz, Tom Walsh, Michail Spiliopoulos et al. · Fertility and Sterility · 2011 · 96 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +6

Esophageal Achalasia: An Uncommon Complication during Pregnancy Treated Conservatively

Dimitrios Spiliopoulos, Michail Spiliopoulos, Alero Awala · Case Reports in Obstetrics and Gynecology · 2013 · 66 citations · Full text

Esophageal Achalasia, Esophagus, Pediatric Swallowing +12