Bhooma Thiruvahindrapuram

ORCID

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 12

Top Venues

Nature genetics

Molecular psychiatry

European journal of human genetics : EJHG

BMC medical genomics

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

Publications

Darcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, Neal Sondheimer, Bhooma Thiruvahindrapuram, Jeffrey R MacDonald, Edward J Higginbotham, Ritesh Thapa, Tarannum Behlim, Sabrina Aimola, Lauren Switzer, Pamela Ng, John Wei, Prakroothi S Danthi, Giovanna Pellecchia, Sylvia Lamoureux, Karen Ho, Sergio L Pereira, Jill de Rijke, Wilson W L Sung, Alireza Mowjoodi, Jennifer L Howe, Thomas Nalpathamkalam, Roozbeh Manshaei, Siavash Ghaffari, Joseph Whitney, Rohan V Patel, Omar Hamdan, Rulan Shaath, Brett Trost, Shannon Knights, Dawa Samdup, Anna McCormick, Carolyn Hunt, Adam Kirton, Anne Kawamura, Ronit Mesterman, Jan Willem Gorter, Nomazulu Dlamini, Daniele Merico, Murto Hilali, Kyle Hirschfeld, Kritika Grover, Nelson X Bautista, Kara Han, Christian R Marshall, Ryan K C Yuen, Padmaja Subbarao, Meghan B Azad, Stuart E Turvey, Piush Mandhane, Theo J Moraes, Elinor Simons, George Maxwell, Michael Shevell, Gregory Costain, Jacques L Michaud, Fadi F Hamdan, Julie Gauthier, Kévin Uguen, Dimitri J Stavropoulos, Richard F Wintle, Maryam Oskoui, Stephen W Scherer
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy. Nature genetics (2024)
Darcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, Neal Sondheimer, Bhooma Thiruvahindrapuram, Jeffrey R MacDonald, Edward J Higginbotham, Ritesh Thapa, Tarannum Behlim, Sabrina Aimola, Lauren Switzer, Pamela Ng, John Wei, Prakroothi S Danthi, Giovanna Pellecchia, Sylvia Lamoureux, Karen Ho, Sergio L Pereira, Jill de Rijke, Wilson W L Sung, Alireza Mowjoodi, Jennifer L Howe, Thomas Nalpathamkalam, Roozbeh Manshaei, Siavash Ghaffari, Joseph Whitney, Rohan V Patel, Omar Hamdan, Rulan Shaath, Brett Trost, Shannon Knights, Dawa Samdup, Anna McCormick, Carolyn Hunt, Adam Kirton, Anne Kawamura, Ronit Mesterman, Jan Willem Gorter, Nomazulu Dlamini, Daniele Merico, Murto Hilali, Kyle Hirschfeld, Kritika Grover, Nelson X Bautista, Kara Han, Christian R Marshall, Ryan K C Yuen, Padmaja Subbarao, Meghan B Azad, Stuart E Turvey, Piush Mandhane, Theo J Moraes, Elinor Simons, George Maxwell, Michael Shevell, Gregory Costain, Jacques L Michaud, Fadi F Hamdan, Julie Gauthier, Kévin Uguen, Dimitri J Stavropoulos, Richard F Wintle, Maryam Oskoui, Stephen W Scherer
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy. Nature genetics 56 (4) (2024)
Darcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, Neal Sondheimer, Bhooma Thiruvahindrapuram, Jeffrey R MacDonald, Edward J Higginbotham, Ritesh Thapa, Tarannum Behlim, Sabrina Aimola, Lauren Switzer, Pamela Ng, John Wei, Prakroothi S Danthi, Giovanna Pellecchia, Sylvia Lamoureux, Karen Ho, Sergio L Pereira, Jill de Rijke, Wilson W L Sung, Alireza Mowjoodi, Jennifer L Howe, Thomas Nalpathamkalam, Roozbeh Manshaei, Siavash Ghaffari, Joseph Whitney, Rohan V Patel, Omar Hamdan, Rulan Shaath, Brett Trost, Shannon Knights, Dawa Samdup, Anna McCormick, Carolyn Hunt, Adam Kirton, Anne Kawamura, Ronit Mesterman, Jan Willem Gorter, Nomazulu Dlamini, Daniele Merico, Murto Hilali, Kyle Hirschfeld, Kritika Grover, Nelson X Bautista, Kara Han, Christian R Marshall, Ryan K C Yuen, Padmaja Subbarao, Meghan B Azad, Stuart E Turvey, Piush Mandhane, Theo J Moraes, Elinor Simons, George Maxwell, Michael Shevell, Gregory Costain, Jacques L Michaud, Fadi F Hamdan, Julie Gauthier, Kévin Uguen, Dimitri J Stavropoulos, Richard F Wintle, Maryam Oskoui, Stephen W Scherer
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy. Nature genetics 56 (4) (2024)
Darcy L Fehlings, Mehdi Zarrei, Worrawat Engchuan, Neal Sondheimer, Bhooma Thiruvahindrapuram, Jeffrey R MacDonald, Edward J Higginbotham, Ritesh Thapa, Tarannum Behlim, Sabrina Aimola, Lauren Switzer, Pamela Ng, John Wei, Prakroothi S Danthi, Giovanna Pellecchia, Sylvia Lamoureux, Karen Ho, Sergio L Pereira, Jill de Rijke, Wilson W L Sung, Alireza Mowjoodi, Jennifer L Howe, Thomas Nalpathamkalam, Roozbeh Manshaei, Siavash Ghaffari, Joseph Whitney, Rohan V Patel, Omar Hamdan, Rulan Shaath, Brett Trost, Shannon Knights, Dawa Samdup, Anna McCormick, Carolyn Hunt, Adam Kirton, Anne Kawamura, Ronit Mesterman, Jan Willem Gorter, Nomazulu Dlamini, Daniele Merico, Murto Hilali, Kyle Hirschfeld, Kritika Grover, Nelson X Bautista, Kara Han, Christian R Marshall, Ryan K C Yuen, Padmaja Subbarao, Meghan B Azad, Stuart E Turvey, Piush Mandhane, Theo J Moraes, Elinor Simons, George Maxwell, Michael Shevell, Gregory Costain, Jacques L Michaud, Fadi F Hamdan, Julie Gauthier, Kévin Uguen, Dimitri J Stavropoulos, Richard F Wintle, Maryam Oskoui, Stephen W Scherer
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy. Nature genetics 56 (4) (2024)
Bushra Haque, David Cheerie, Saba Birkadze, Alice Linyan Xu, Thomas Nalpathamkalam, Bhooma Thiruvahindrapuram, Susan Walker, Gregory Costain
Estimating the proportion of nonsense variants undergoing the newly described phenomenon of manufactured splice rescue. European journal of human genetics : EJHG (2023)
Shengjie Ying, Tracy Heung, Bhooma Thiruvahindrapuram, Worrawat Engchuan, Yue Yin, Christina Blagojevic, Zhaolei Zhang, Robert A Hegele, Ryan K C Yuen, Danielle S Bassett
Polygenic risk for triglyceride levels in the presence of a high impact rare variant. BMC medical genomics 16 (1) (2023)
Claudia I Samogy Costa, Gabriele Campos, Eduarda Morgana da Silva Montenegro, Jaqueline Yu Ting Wang, Marília Scliar, Frederico Monfardini, Elaine Cristina Zachi, Naila C V Lourenço, Ada J S Chan, Sergio L Pereira, Worrawat Engchuan, Bhooma Thiruvahindrapuram, Mehdi Zarrei, Stephen W Scherer, Maria Rita Passos-Bueno
Three generation families: Analysis of de novo variants in autism. European journal of human genetics : EJHG (2023)
Ada J S Chan, Worrawat Engchuan, Miriam S Reuter, Zhuozhi Wang, Bhooma Thiruvahindrapuram, Brett Trost, Thomas Nalpathamkalam, Carol Negrijn, Sylvia Lamoureux, Giovanna Pellecchia, Rohan V Patel, Wilson W L Sung, Jeffrey R MacDonald, Jennifer L Howe, Jacob A S Vorstman, Neal Sondheimer, Nicole Takahashi, Judith H Miles, Evdokia Anagnostou, Kristiina Tammimies, Mehdi Zarrei, Daniele Merico, Dimitri J Stavropoulos, Ryan K C Yuen, Bridget A Fernandez, Stephen W Scherer
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder. Nature communications 13 (1) (2022)
Robert Lesurf, Abdelrahman Said, Oyediran Akinrinade, Jeroen Breckpot, Kathleen Delfosse, Ting Liu, Roderick Yao, Gabrielle Persad, Fintan McKenna, Ramil R Noche, Winona Oliveros, Kaia Mattioli, Shreya Shah, Anastasia Miron, Qian Yang, Guoliang Meng, Michelle Chan Seng Yue, Wilson W L Sung, Bhooma Thiruvahindrapuram, Jane Lougheed, Erwin Oechslin, Tapas Mondal, M Lynn Bergin, John Smythe, Shashank Jayappa, Vinay J Rao, Jayaprakash Shenthar, Perundurai S Dhandapany, Christopher Semsarian, Robert G Weintraub, Richard Douglas Bagnall, Jodie Ingles, null null, Marta Melé, Philipp G Maass, James Ellis, Stephen W Scherer, Seema Mital
Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy. NPJ genomic medicine 7 (1) (2022)
Bahareh A Mojarad, Worrawat Engchuan, Brett Trost, Ian Backstrom, Yue Yin, Bhooma Thiruvahindrapuram, Linda Pallotto, Aleksandra Mitina, Mahreen Khan, Giovanna Pellecchia, Bushra Haque, Keyi Guo, Tracy Heung, Gregory Costain, Stephen W Scherer, Christian R Marshall, Christopher E Pearson, Anne Susan Bassett, Ryan K C Yuen
Genome-wide tandem repeat expansions contribute to schizophrenia risk. Molecular psychiatry 27 (9) (2022)
Adam X Maihofer, Worrawat Engchuan, Guillaume Huguet, Marieke Klein, Jeffrey R MacDonald, Omar Shanta, Bhooma Thiruvahindrapuram, Martineau Jean-Louis, Zohra Saci, Sebastien Jacquemont, Stephen W Scherer, Elizabeth Ketema, Allison E Aiello, Ananda B Amstadter, Esmina Avdibegović, Dragan Babic, Dewleen G Baker, Jonathan I Bisson, Marco P M Boks, Elizabeth A Bolger, Richard A Bryant, Angela C Bustamante, Jose Miguel Caldas-de-Almeida, Graça Cardoso, Jurgen Deckert, Douglas L Delahanty, Katharina Domschke, Boadie W Dunlop, Alma Dzubur-Kulenovic, Alexandra Evans, Norah C Feeny, Carol E Franz, Aarti Gautam, Elbert Geuze, Aferdita Goci, Rasha Hammamieh, Miro Jakovljevic, Marti Jett, Ian R Jones, Milissa L Kaufman, Ronald C Kessler, Anthony P King, William S Kremen, Bruce R Lawford, Lauren A M Lebois, Catrin Lewis, Israel Liberzon, Sarah D Linnstaedt, Bozo Lugonja, Jurjen J Luykx, Michael J Lyons, Matig R Mavissakalian, Katie A McLaughlin, Samuel A McLean, Divya Mehta, Rebecca Mellor, Charles Phillip Morris, Seid Muhie, Holly K Orcutt, Matthew Peverill, Andrew Ratanatharathorn, Victoria B Risbrough, Albert Skip Rizzo, Andrea L Roberts, Alex O Rothbaum, Barbara O Rothbaum, Peter Roy-Byrne, Kenneth J Ruggiero, Bart P F Rutten, Dick Schijven, Julia S Seng, Christina M Sheerin, Michael A Sorenson, Martin Hersch Teicher, Monica Uddin, Robert J Ursano, Christiaan H Vinkers, Joanne Voisey, Heike Weber, Sherry Winternitz, Miguel Xavier, Ruoting Yang, Ross McD Young, Lori A Zoellner, null null, null null, Rany M Salem, Richard A Shaffer, Tianying Wu, Kerry James Ressler, Murray B Stein, Karestan C Koenen, Jonathan Sebat, Caroline M Nievergelt
Rare copy number variation in posttraumatic stress disorder. Molecular psychiatry (2022)
Jia Wen, Brett Trost, Worrawat Engchuan, Matthew Halvorsen, Linda M Pallotto, Aleksandra Mitina, NaEshia Ancalade, Martilias S Farrell, Ian Backstrom, Keyi Guo, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, Paola Giusti-Rodriguez, Jonathan David Rosen, Yun Li, Hyejung Won, Patrik K E Magnusson, Ulf Gyllensten, Anne Susan Bassett, Christina M Hultman, Patrick F Sullivan, Ryan K C Yuen, Jin P Szatkiewicz
Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia. Molecular psychiatry (2022)

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Publication Activity (10 Years)

Top Topics

Top Venues

Bhooma Thiruvahindrapuram