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Cited by in CrossRef
Number Cited Articles
1
Maria Piccione, Tiziana Fragapane, Vincenzo Antona, Daniela Giachino, Francesco Cupido, Giovanni Corsello. Response to Stanich et al.: Correspondence regarding-PTEN hamartoma tumor syndromes in childhood-Description of two cases and a proposal for follow-up protocolAmerican Journal of Medical Genetics Part A 2014; 164(7): 1871 doi: 10.1002/ajmg.a.36527
2
Monika M. Golas, Bernd Auber, Tim Ripperger, Brigitte Pabst, Gunnar Schmidt, Michel Morlot, Uta Diebold, Doris Steinemann, Brigitte Schlegelberger, Susanne Morlot. Looking for the hidden mutation: Bannayan–Riley–Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A American Journal of Medical Genetics Part A 2019;  doi: 10.1002/ajmg.a.61166
3
Shlomi Cohen, Warren Hyer, Emmanuel Mas, Marcus Auth, Thomas M. Attard, Johannes Spalinger, Andrew Latchford, Carol Durno. Management of Juvenile Polyposis Syndrome in Children and AdolescentsJournal of Pediatric Gastroenterology and Nutrition 2019; 68(3): 453 doi: 10.1097/MPG.0000000000002246
4
Till Joscha Demal, Melina Heise, Benedikt Reiz, Deepika Dogra, Ingrid Brænne, Hermann Reichenspurner, Jörg Männer, Zouhair Aherrahrou, Heribert Schunkert, Jeanette Erdmann, Salim Abdelilah-Seyfried. A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1AScientific Reports 2019; 9(1) doi: 10.1038/s41598-019-39648-7
5
Richard N. Wang, Jordan Green, Zhongliang Wang, Youlin Deng, Min Qiao, Michael Peabody, Qian Zhang, Jixing Ye, Zhengjian Yan, Sahitya Denduluri, Olumuyiwa Idowu, Melissa Li, Christine Shen, Alan Hu, Rex C. Haydon, Richard Kang, James Mok, Michael J. Lee, Hue L. Luu, Lewis L. Shi. Bone Morphogenetic Protein (BMP) signaling in development and human diseasesGenes & Diseases 2014; 1(1): 87 doi: 10.1016/j.gendis.2014.07.005
6
Federica Guaraldi, Giovanni Di Nardo, Luigi Tarani, Luca Bertelli, Francesco Claudio Susca, Rosanna Bagnulo, Nicoletta Resta. Association of autoimmune thyroiditis and celiac disease with Juvenile Polyposis due to 10q23.1q23.31 deletion: Potential role of PI3K/Akt pathway dysregulationEuropean Journal of Medical Genetics 2017; 60(7): 380 doi: 10.1016/j.ejmg.2017.04.010