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Home - The Girirajan Laboratory

What is the molecular genetic basis of neurodevelopmental disorders? Welcome to the Girirajan Lab website! The primary focus of our research is to discover and characterize genetic changes including genomic deletions and duplications and single nucleotide mutations contributing to neurodevelopmental disorders such as autism, intellectual disability, schizophrenia, epilepsy and congenital malformation. The Girirajan laboratory is affiliated to the following:. The Huck Institutes of the Life Sciences.

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Home - The Girirajan Laboratory | autism.bx.psu.edu Reviews

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What is the molecular genetic basis of neurodevelopmental disorders? Welcome to the Girirajan Lab website! The primary focus of our research is to discover and characterize genetic changes including genomic deletions and duplications and single nucleotide mutations contributing to neurodevelopmental disorders such as autism, intellectual disability, schizophrenia, epilepsy and congenital malformation. The Girirajan laboratory is affiliated to the following:. The Huck Institutes of the Life Sciences.

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Home - The Girirajan Laboratory | autism.bx.psu.edu Reviews

https://autism.bx.psu.edu

What is the molecular genetic basis of neurodevelopmental disorders? Welcome to the Girirajan Lab website! The primary focus of our research is to discover and characterize genetic changes including genomic deletions and duplications and single nucleotide mutations contributing to neurodevelopmental disorders such as autism, intellectual disability, schizophrenia, epilepsy and congenital malformation. The Girirajan laboratory is affiliated to the following:. The Huck Institutes of the Life Sciences.

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autism.bx.psu.edu

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Teaching - The Girirajan Laboratory

https://autism.bx.psu.edu/teaching.html

I teach two courses, Genomics. For graduate students in the Fall semester and Functional Genomics. Contact webmaster: mpj5142@psu.edu.

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The project | 16p12.2 deletion study - The Girirajan Laboratory

https://autism.bx.psu.edu/16p12.2

Our work would not be possible without the recruitment of patients for study. We invite you to participate in our study if your child or loved one of yours has been affected by the 16p12.2 deletion. Contact webmaster: mpj5142@psu.edu.

3

People - The Girirajan Laboratory

https://autism.bx.psu.edu/people.html

Lab photo 2014 - From left to right: Janani Iyer, Lizmari Reyez-Munoz, Lexi Kubina, Abby Talbert, Brian Lifshutz, Santhosh Girirajan, Thanh Le, Qingyu Wang, Komal Vadodaria, Andrew Polyak, Lucilla Pizzo. Qingyu Wang, Graduate student (PhD class of 2016). Janani Iyer, Postdoctoral scholar. Andrew Polyak, Research technologist. Thanh Le, Rotation graduate student. Janine Brandt, Undergraduate student. Lauren Thomas, Undergraduate student. Abigail Talbert, Undergraduate student.

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Publications - The Girirajan Laboratory

https://autism.bx.psu.edu/publications.html

Quantitative Assessment of Eye Phenotypes for Functional Genetic Studies Using Drosophila melanogaster. Iyer J, Wang Q, Le T, Pizzo L. Gronke S, Ambegaokar S, Imai Y, Srivastava A, Llamusi Troisi B, Mardon G, Artero R, Jackson GR, Isaacs AM, Partridge L, Kumar JP, Girirajan S. An assessment of sex bias in neurodevelopmental disorders. Rosenfeld JA, Girirajan S. Comorbidity of intellectual disability confounds ascertainment of autism: implications for genetic diagnosis. Kubina RM, Girirajan S. Zhao N, Wu ...

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Participate | 16p12.2 deletion study - The Girirajan Laboratory

https://autism.bx.psu.edu/16p12.2/participate.html

The following is an initial questionnaire used to gain information about you, and the affected individual carrying deletion 16p12.2 (previously known as 16p12.1 deletion). This questionnaire is designed for parents or guardians of children diagnosed with this deletion. The information provided in this questionnaire will be used to better understand the connection between the symptoms these individuals manifest, and genetic variation identified. Continue to electronic survey.

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News - Craig Cameron Lab

http://www.cameronlab.com/news

Website about the members and research of the lab of Craig Cameron, PhD, at The Pennylvania State University. August 5th, 2016. Friend and colleague, Squire Booker, featured on the homepage of the Howard Hughes Medical Institute. When he is no longer the face of the homepage, you can still read about him here. May 19th, 2016. Plenary and award lectures from the 2016 Annual Meeting of the American Society for Biochemistry and Molecular Biology are now online ( click here. Harvard University, HHMI. Penn St...

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Home - The Girirajan Laboratory

What is the molecular genetic basis of neurodevelopmental disorders? Welcome to the Girirajan Lab website! The primary focus of our research is to discover and characterize genetic changes including genomic deletions and duplications and single nucleotide mutations contributing to neurodevelopmental disorders such as autism, intellectual disability, schizophrenia, epilepsy and congenital malformation. The Girirajan laboratory is affiliated to the following:. The Huck Institutes of the Life Sciences.

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