GabrielAlejandroBien-WillnerMD

PubMed

• 18 citations
  A multigene mutation classification of 468 colorectal cancers reveals a prognostic role for APC.
  Schell, M. J., Yang, M., Teer, J. K., Lo, F. Y., Madan, A., Coppola, D., Monteiro, A. N., Nebozhyn, M. V., Yue, B., Loboda, A., Bien-Willner, G. A., Greenawalt, D. M.,...> ;Nature communications. 2016 Jun 16
• Genetic variation in MKL2 and decreased downstream PCTAIRE1 expression in extreme, fatal primary human microcephaly.
  Ramos EI Bien-Willner GA Li J Hughes AE Giacalone J Chasnoff S Kulkarni S Parmacek M Cole FS Druley TE> ;Clin Genet. 2014 May
• 19 citations
  CD163 Immunohistochemistry Is Superior to CD68 in Predicting Outcome in Classical Hodgkin Lymphoma
  Jonathan L. Klein, Tu Dung T. Nguyen, Gabriel A. Bien-Willner, Ling Chen, Kelley V. Foyil, Nancy L. Bartlett, Eric J. Duncavage, Anjum Hassan, John L. Frater, Friederi...> ;American Journal of Clinical Pathology. 2014 Mar 1
• Male-to-female sex reversal associated with an ∼250 kb deletion upstream of NR0B1 (DAX1)
  Marta Smyk, Jonathan S. Berg, Amber Pursley, Fiona Curtis, Bridget A. Fernandez, Gabriel A. Bien-Willner, James R. Lupski, Sau Wai Cheung, Pawel Stankiewicz> ;Human Genetics. 2007 May 15
• SOX9cre1, a cis-acting regulatory element located 1.1 Mb upstream of SOX9, mediates its enhancement through the SHH pathway.
  Gabriel A. Bien-Willner, Pawel Stankiewicz, James R. Lupski> ;Human Molecular Genetics. 2007 May 15
• Two novel translocation breakpoints upstream of SOX9 define borders of the proximal and distal breakpoint cluster region in campomelic dysplasia.
  M Leipoldt, M Erdel, Gabriel A. Bien-Willner, Marta Smyk, M Theurl, Svetlana A. Yatsenko, J R Lupski, AH Lane, AL Shanske, Pawel Stankiewicz, Gerd Scherer> ;Clinical Genetics. 2006 Dec 14
• Mutational and genotype-phenotype correlation analyses in 28 polish patients with cornelia de lange syndrome
  Jiong Yan, Gulam Mustafa Saifi, Tomasz H. Wierzba, Marjorie Withers, Gabriel A. Bien-Willner, Janusz Limon, Pawel Stankiewicz, James R. Lupski, Jolanta Wierzba> ;American Journal of Medical Genetics Part A. 2006 Jul 15
• 69 citations
  Position effects due to chromosome breakpoints that map ∼900 Kb upstream and ∼1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia
  Gopalrao V.N. Velagaleti, Gabriel A. Bien-Willner, Jill K. Northup, Lillian H. Lockhart, Judy C. Hawkins, Syed M. Jalal, Marjorie Withers, James R. Lupski, Pawel Stank...> ;American Journal of Human Genetics. 2005 Apr 1
• 14 citations
  Small marker chromosomes in two patients with segmental aneusomy for proximal 17p
  Christine J. Shaw, Pawel Stankiewicz, Gabriel A. Bien-Willner, Scott C. Bello, Chad A. Shaw, Marta Carrera, Luis A. Pérez Jurado, Xavier Estivill, James R. Lupski> ;Human Genetics. 2004 Apr 20
• Join now to see all

Journal Articles

• Mutation and expression analysis in medulloblastoma yields prognostic variants and a putative mechanism of disease for i17q tumors  
  Bien-Willner GA, Mitra RD, Acta Neuropathol Commun, 7/17/2014
• Early recurrence in standard-risk medulloblastoma patients with the common idic(17)(p11.2) rearrangement  
  Bien-Willner, GA, López-Terrada D, Bhattacharjee MB, Patel KU, Stankiewicz P, Lupski JR, Pfeifer JR, Perry A, Neuro-Oncology, 3/13/2012

Lectures

• Analysis of use of a molecular reporting and treatment decision support tool in more than 1300 cancer cases. 
  2018 ASCO Annual Meeting - Chicago, Illinois - 06/2/2018