Neurofibromatosis Type 2 (NF2) and the Implications for Vestibular Schwannoma and Meningioma Pathogenesis
Bachir, Suha, Shah, Sanjit, Shapiro, Scott, Koehler, Abigail, Mahammedi, Abdelkader, Samy, Ravi N, Zuccarello, Mario, Schorry, Elizabeth, Sengupta, Soma
Published in International journal of molecular sciences (12.01.2021)
Published in International journal of molecular sciences (12.01.2021)
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Journal Article
A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndrome
Doyle, Jefferson J, Doyle, Alexander J, Wilson, Nicole K, Habashi, Jennifer P, Bedja, Djahida, Whitworth, Ryan E, Lindsay, Mark E, Schoenhoff, Florian, Myers, Loretha, Huso, Nick, Bachir, Suha, Squires, Oliver, Rusholme, Benjamin, Ehsan, Hamid, Huso, David, Thomas, Craig J, Caulfield, Mark J, Van Eyk, Jennifer E, Judge, Daniel P, Dietz, Harry C
Published in eLife (27.10.2015)
Published in eLife (27.10.2015)
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Journal Article
P639: Large-scale genome reanalysis of 159 individuals affected by undiagnosed genetic diseases from the Stanford Center for Undiagnosed Diseases
Mendez, Hector, Bonner, Devon, Reuter, Chloe, Kohler, Jennefer, Marwaha, Shruti, van de Wiel, Laurens, Kravets, Elijah, Ostrow, Charlotte, Alvarez, Raquel, Emami, Sara, Halley, Meghan, Tabor, Holly, Bachir, Suha, Bernstein, Jonathan, Wheeler, Matthew
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Imaging of Neurologic Disease in Hospitalized Patients with COVID-19: An Italian Multicenter Retrospective Observational Study
Mahammedi, Abdelkader, Saba, Luca, Vagal, Achala, Leali, Michela, Rossi, Andrea, Gaskill, Mary, Sengupta, Soma, Zhang, Bin, Carriero, Alessandro, Bachir, Suha, Crivelli, Paola, Paschè, Alessio, Premi, Enrico, Padovani, Alessandro, Gasparotti, Roberto
Published in Radiology (01.11.2020)
Published in Radiology (01.11.2020)
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Journal Article
Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant
Smith, Carly M., Guinon, Kristi, Bachir, Suha, Tise, Christina G.
Published in Prenatal diagnosis (01.08.2024)
Published in Prenatal diagnosis (01.08.2024)
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Journal Article
Is There a Genetic Correlation between Multiple Sclerosis and Cerebral Aneurysms?
Albrekkan, Fatimah M, Bachir, Suha, Jumaa, Mouhammed A, Zaidi, Syed Fazal, Medhkour, Azedine
Published in World neurosurgery (01.11.2016)
Published in World neurosurgery (01.11.2016)
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Journal Article
A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with a PTPN11 mutation and a novel variant in SOS1
Fahrner, Jill A., Frazier, Aisha, Bachir, Suha, Walsh, Michael F., Applegate, Carolyn D., Thompson, Reid, Halushka, Marc K., Murphy, Anne M., Gunay‐Aygun, Meral
Published in American journal of medical genetics. Part A (01.06.2012)
Published in American journal of medical genetics. Part A (01.06.2012)
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Journal Article
A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with a PTPN11 mutation and a novel variant in SOS1
Fahrner, Jill A., Frazier, Aisha, Bachir, Suha, Walsh, Michael F., Applegate, Carolyn D., Thompson, Reid, Halushka, Marc K., Murphy, Anne M., Gunay-Aygun, Meral
Published in American Journal of Medical Genetics Part A (01.06.2012)
Published in American Journal of Medical Genetics Part A (01.06.2012)
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