Thashi Bharadwaj

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 16

Top Topics

Intellectual Disability

Autism Spectrum Disorder

Top Venues

BioMed research international

Brain communications

Molecular genetics & genomic medicine

European journal of human genetics : EJHG

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)
Diana M Cornejo-Sanchez, Anushree Acharya, Thashi Bharadwaj, Lizeth Marin-Gomez, Pilar Pereira-Gomez, Liz M Nouel-Saied, null University Of Washington Center For Mendelian Genomics, Deborah A Nickerson, Michael J Bamshad, Heather C Mefford, Isabelle Schrauwen, Jaime Carrizosa-Moog, William Cornejo-Ochoa, Nicolas Pineda-Trujillo, Suzanne M Leal
SCN1A Variants as the Underlying Cause of Genetic Epilepsy with Febrile Seizures Plus in Two Multi-Generational Colombian Families. Genes 13 (5) (2022)
Abdoulaye Yalcouyé, Oumou Traoré, Salimata Diarra, Isabelle Schrauwen, Kevin Esoh, Magda Kamila Kadlubowska, Thashi Bharadwaj, Samuel Mawuli Adadey, Mohamed Kéita, Cheick O Guinto, Suzanne M Leal, Guida Landouré, Ambroise Wonkam
A monoallelic variant in EYA1 is associated with Branchio-Otic syndrome in a Malian family. Molecular genetics & genomic medicine 10 (7) (2022)
Isabelle Schrauwen, Amama Ghaffar, Thashi Bharadwaj, Khadim Shah, Sakina Rehman, Anushree Acharya, Khurram Liaqat, Nicole S Lin, Jenna L Everard, Anwar Khan, Zubair M Ahmed, Wasim Ahmad, Saima Riazuddin, Regie Lyn P Santos-Cortez
Syntaxin 4 is essential for hearing in human and zebrafish. Human molecular genetics (2022)
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)
Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Suzanne M Leal, Ambroise Wonkam
A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family. Experimental biology and medicine (Maywood, N.J.) 246 (13) (2021)
Adebolajo A Adeyemo, Rabia Faridi, Parna Chattaraj, Rizwan Yousaf, Risa Tona, Samuel Okorie, Thashi Bharadwaj, Liz M Nouel-Saied, Anushree Acharya, Isabelle Schrauwen, Robert J Morell, Regie Lyn P Santos-Cortez, Thomas B Friedman, Andrew J Griffith, Isabelle Roux
Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria. European journal of human genetics : EJHG (2021)
Thashi Bharadwaj, Isabelle Schrauwen, Sakina Rehman, Khurram Liaqat, Anushree Acharya, Arnaud P J Giese, Liz M Nouel-Saied, Abdul Nasir, Jenna L Everard, Lana M Pollock, Shaoyuan Zhu, Michael J Bamshad, Deborah A Nickerson, Raja Hussain Ali, Asmat Ullah, Abdul Wali, Ghazanfar Ali, Regie Lyn P Santos-Cortez, Zubair M Ahmed, Brian M McDermott, Muhammad Ansar, Saima Riazuddin, Wasim Ahmad, Regie Lyn P Santos-Cortez
ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment. European journal of human genetics : EJHG (2021)
Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Samuel Mawuli Adadey, Shaheen Mowla, Suzanne M Leal, Ambroise Wonkam
Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment. Genes 11 (11) (2020)