Harsha Prasada Lashkari

ORCID

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 4

Top Venues

Clinical case reports

Human mutation

Nature genetics

Indian journal of pediatrics

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

Publications

Shalini Radhakrishnan, Ranjitha Rao, Harsha Prasada Lashkari, Hema Kini, Jyoti Ramanath Kini, Vatsala Basavaraju Kudurugundi, Vanishree Ashok, Chaithra Venkataramana Gowthuvalli
A needle in the haystack: An unusual case presentation of ganglioneuroblastoma at a tertiary care center in Coastal Karnataka. Clinical case reports 11 (11) (2023)
Ricardo Moreno Traspas, Tze Shin Teoh, Pui-Mun Wong, Michael Maier, Crystal Y Chia, Kenneth Lay, Nur Ain Ali, Austin Larson, Fuad Al Mutairi, Nouriya Abbas Al-Sannaa, Eissa Ali Faqeih, Majid Alfadhel, Huma Arshad Cheema, Juliette Dupont, Stephane Bezieau, Bertrand Isidor, Dorrain Yanwen Low, Yulan Wang, Grace Tan, Poh San Lai, Hugues Piloquet, Madeleine Joubert, Hülya Kayserili, Kimberly A Kripps, Shareef A Nahas, Eric P Wartchow, Mikako Warren, Gandham SriLakshmi Bhavani, Majed Dasouki, Renata Sandoval, Elisa Carvalho, Luiza Ramos, Gilda Porta, Bin Wu, Harsha Prasada Lashkari, Badr AlSaleem, Raeda M BaAbbad, Anabela Natália Abreu Ferrão, Vasiliki Karageorgou, Natalia Ordonez-Herrera, Suliman Khan, Peter Bauer, Benjamin Cogné, Aida Maria Bertoli-Avella, Marie Vincent, Katta Mohan Girisha, Bruno Reversade
Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis. Nature genetics 54 (8) (2022)
Merin George, Avani Solanki, Niranjan Chavan, Aruna Rajendran, Revathi Raj, Sheila Mohan, Sandeep Nemani, Shailesh Kanvinde, Deendayalan Munirathnam, Sudha Rao, Nita Radhakrishnan, Harsha Prasada Lashkari, Radha Gulati Ghildhiyal, Mamta Manglani, Chandrakala Shanmukhaiah, Sunil Bhat, Sowmyashree Ramesh, Anchu Cherian, Pritesh Junagade, Babu Rao Vundinti
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects. Human mutation 42 (12) (2021)
Harsha Prasada Lashkari, Manisha Madkaikar, Aparna Dalvi, Maya Gupta, Jacinta Bustamante, Madhubala Sharma, Amit Rawat, Prateek Bhatia, Kamalakshi G Bhat, Sadashiva Rao, Nutan Kamath, Faheem Moideen, Sylvain Latour, Sarah Winter, Gandham SriLakshmi Bhavani, Katta M Girisha
Clinical and Genetic Spectrum of Inborn Errors of Immunity in a Tertiary Care Center in Southern India. Indian journal of pediatrics (2021)

Harsha Prasada Lashkari

Publication Activity (10 Years)

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