Élise Schaefer

Top papers

• “Bold! Daring! Shocking! True!”

  Élise Schaefer·1999
  ↗ 446
• New perspectives on community-acquired pneumonia in 388 406 patients. Results from a nationwide mandatory performance measurement programme in healthcare quality

  Santiago Ewig, Norbert Birkner, Richard Strauß, et al.·2009·Thorax
  ↗ 408OA
• Postpartum Anxiety and Maternal-Infant Health Outcomes

  Ian M. Paul, Danielle Symons Downs, Élise Schaefer, et al.·2013·PEDIATRICS
  ↗ 222
• Early Weight Loss Nomograms for Exclusively Breastfed Newborns

  Valerie J. Flaherman, Élise Schaefer, Michael W. Kuzniewicz, et al.·2014·PEDIATRICS
  ↗ 196OA
• Breastfeeding Outcome Comparison by Parity

  Nicole M. Hackman, Élise Schaefer, Jessica S. Beiler, et al.·2014·Breastfeeding Medicine
  ↗ 177OA
• Idiopathic Systemic Capillary Leak Syndrome (Clarkson's Disease): The Mayo Clinic Experience

  Prashant Kapoor, Patricia T. Greipp, Élise Schaefer, et al.·2010·Mayo Clinic Proceedings
  ↗ 172OA
• Treacher Collins syndrome: a clinical and molecular study based on a large series of patients

  Marie Vincent, David Geneviève, Agnès Ostertag, et al.·2015·Genetics in Medicine
  ↗ 161
• Defining the phenotypic spectrum of <i>SLC6A1</i> mutations

  Katrine M. Johannesen, Elena Gardella, Tarja Linnankivi, et al.·2018·Epilepsia
  ↗ 148OA
• Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit <i>BBIP1</i> (<i>BBS18</i>)

  Sophie Scheidecker, Christelle Etard, Nathan W. Pierce, et al.·2013·Journal of Medical Genetics
  ↗ 137OA
• Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy

  Johann Böhm, Valérie Biancalana, Elizabeth T. DeChene, et al.·2012·Human Mutation
  ↗ 136OA
• Truven Health Analytics MarketScan Databases for Clinical Research in Colon and Rectal Surgery

  Élise Schaefer, Evangelos Messaris, Christopher S. Hollenbeak, et al.·2019·Clinics in Colon and Rectal Surgery
  ↗ 129OA
• Exome sequencing identifies mutations in <i>LZTFL1</i>, a BBSome and smoothened trafficking regulator, in a family with Bardet–Biedl syndrome with situs inversus and insertional polydactyly

  Vincent Marion, Fanny Stutzmann, Marion Gérard, et al.·2012·Journal of Medical Genetics
  ↗ 128