Anushree Acharya

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 10

Top Topics

Duchenne Muscular Dystrophy

Intellectual Disability

Autism Spectrum Disorder

Top Venues

BioMed research international

Brain communications

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Irma Järvelä, Ritva Paetau, Yasmin Rajendran, Anushree Acharya, Thashi Bharadwaj, Suzanne M Leal, Anna-Elina Lehesjoki, Maarit Palomäki, Isabelle Schrauwen
Heterogeneous genetic patterns in bilateral perisylvian polymicrogyria: insights from a Finnish family cohort. Brain communications 6 (3) (2024)
Irma Järvelä, Ritva Paetau, Yasmin Rajendran, Anushree Acharya, Thashi Bharadwaj, Suzanne M Leal, Anna-Elina Lehesjoki, Maarit Palomäki, Isabelle Schrauwen
Heterogeneous genetic patterns in bilateral perisylvian polymicrogyria: insights from a Finnish family cohort. Brain communications 6 (3) (2024)
Irma Järvelä, Ritva Paetau, Yasmin Rajendran, Anushree Acharya, Thashi Bharadwaj, Suzanne M Leal, Anna-Elina Lehesjoki, Maarit Palomäki, Isabelle Schrauwen
Heterogeneous genetic patterns in bilateral perisylvian polymicrogyria: insights from a Finnish family cohort. Brain communications 6 (3) (2024)
Irma Järvelä, Ritva Paetau, Yasmin Rajendran, Anushree Acharya, Thashi Bharadwaj, Suzanne M Leal, Anna-Elina Lehesjoki, Maarit Palomäki, Isabelle Schrauwen
Heterogeneous genetic patterns in bilateral perisylvian polymicrogyria: insights from a Finnish family cohort. Brain communications 6 (3) (2024)
Abrar Hussain, Anushree Acharya, Thashi Bharadwaj, University Of Washington Center For Mendelian Genomics, Regie Lyn P Santos-Cortez, Abdul Khaliq, Asif Mir, Isabelle Schrauwen
A Novel Variant in VPS13B Underlying Cohen Syndrome. BioMed research international 2023 (2023)
Abrar Hussain, Anushree Acharya, Thashi Bharadwaj, University Of Washington Center For Mendelian Genomics, Regie Lyn P Santos-Cortez, Abdul Khaliq, Asif Mir, Isabelle Schrauwen
A Novel Variant in VPS13B Underlying Cohen Syndrome. BioMed research international 2023 (2023)
Abrar Hussain, Anushree Acharya, Thashi Bharadwaj, University Of Washington Center For Mendelian Genomics, Regie Lyn P Santos-Cortez, Abdul Khaliq, Asif Mir, Isabelle Schrauwen
A Novel Variant in VPS13B Underlying Cohen Syndrome. BioMed research international 2023 (2023)
Abrar Hussain, Anushree Acharya, Thashi Bharadwaj, University Of Washington Center For Mendelian Genomics, Regie Lyn P Santos-Cortez, Abdul Khaliq, Asif Mir, Isabelle Schrauwen
A Novel Variant in VPS13B Underlying Cohen Syndrome. BioMed research international 2023 (2023)
Thashi Bharadwaj, Isabelle Schrauwen, Anushree Acharya, Liz M Nouel Saied, Marja-Leena Väisänen, Minna Kraatari, Elisa Rahikkala, Irma Jarvela, Jouko Kotimäki, Regie Lyn P Santos-Cortez
Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant. Molecular genetics & genomic medicine 10 (3) (2022)
Hannaleena Kokkonen, Auli Siren, Tuomo Määttä, Magda Kamila Kadlubowska, Anushree Acharya, Liz M Nouel-Saied, Regie Lyn P Santos-Cortez, Irma Järvelä, Isabelle Schrauwen
Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders. Molecular genetics & genomic medicine (2021)