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Suleyman Gulsuner

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Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|December 10, 2013
De novo mutations in schizophrenia disrupt genes co-expressed in fetal prefrontal cortexSuleyman Gulsuner, Jon M McClellan
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|December 9, 2014
Copy number variation in schizophreniaSuleyman Gulsuner, Jon M McClellan
Ophthalmic Genetics|June 13, 2012
Neuro-ophthalmologic findings in humans with quadrupedal locomotionOzge Sarac, Suleyman Gulsuner, Yelda Yildiz-Tasci, et al.
Journal of Clinical Immunology|May 27, 2022
Revisiting Genetic Testing for Patients with Negative Results: IPEX and FOXP3Sarah K Baxter, Suleyman Gulsuner, David Hagin, et al.
Blood Advances|October 4, 2023
Evaluating the prevalence of inborn errors of immunity in adults with chronic immune thrombocytopenia or Evans syndromeDebbie Jiang, Kira Rosenlind, Sarah Baxter, et al.
Journal of Medical Genetics|October 16, 2020
CRISPR-Cas9/long-read sequencing approach to identify cryptic mutations in <i>BRCA1</i> and other tumour suppressor genesTom Walsh, Silvia Casadei, Katherine M Munson, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 11, 2008
Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humansTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 12, 2008
Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotionTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2025
Genetic regulation of the estrogen receptor and inherited predisposition to breast cancerSarah B Pierce, Hannah Kortbawi, Suleyman Gulsuner, et al.
JAMA Oncology|July 21, 2017
Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish WomenTom Walsh, Jessica B Mandell, Barbara M Norquist, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|December 10, 2013
De novo mutations in schizophrenia disrupt genes co-expressed in fetal prefrontal cortexSuleyman Gulsuner, Jon M McClellan
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|December 9, 2014
Copy number variation in schizophreniaSuleyman Gulsuner, Jon M McClellan
Ophthalmic Genetics|June 13, 2012
Neuro-ophthalmologic findings in humans with quadrupedal locomotionOzge Sarac, Suleyman Gulsuner, Yelda Yildiz-Tasci, et al.
Journal of Clinical Immunology|May 27, 2022
Revisiting Genetic Testing for Patients with Negative Results: IPEX and FOXP3Sarah K Baxter, Suleyman Gulsuner, David Hagin, et al.
Blood Advances|October 4, 2023
Evaluating the prevalence of inborn errors of immunity in adults with chronic immune thrombocytopenia or Evans syndromeDebbie Jiang, Kira Rosenlind, Sarah Baxter, et al.
Journal of Medical Genetics|October 16, 2020
CRISPR-Cas9/long-read sequencing approach to identify cryptic mutations in <i>BRCA1</i> and other tumour suppressor genesTom Walsh, Silvia Casadei, Katherine M Munson, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 11, 2008
Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humansTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 12, 2008
Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotionTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 23, 2025
Genetic regulation of the estrogen receptor and inherited predisposition to breast cancerSarah B Pierce, Hannah Kortbawi, Suleyman Gulsuner, et al.
JAMA Oncology|July 21, 2017
Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish WomenTom Walsh, Jessica B Mandell, Barbara M Norquist, et al.
Pageof 7