Tarjinder Singh

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 27

Top Venues

Nature genetics

Nature aging

European journal of human genetics : EJHG

bioRxiv : the preprint server for biology

Broad Institute

University of Cambridge (PHD)

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

Affiliation History

Broad Institute Feb 01 2017

United States

Postdoctoral Fellow :: Stanley Center of Psychiatric Research

Massachusetts General Hospital Feb 01 2017

United States

Postdoctoral Fellow :: Analytic and Translational Unit/Center of Genomic Medicine

Education History

University of Cambridge Oct 01 2012 - Oct 01 2016

United Kingdom

PHD :: Wellcome Trust Sanger Institute

Williams College Sep 01 2008 - Jun 01 2012

United States

BSC

Publications

Lea Urpa, Mitja I Kurki, Elisa J Rahikkala, Eija Hämäläinen, Veikko V Salomaa, Jaana Suvisaari, Riikka Keski-Filppula, Merja Rauhala, Satu Korpi-Heikkilä, Jonna Komulainen-Ebrahim, Heli Helander, Päivi M Vieira, Johanna Uusimaa, Jukka S Moilanen, Jarmo Körkkö, Tarjinder Singh, Outi Kuismin, Olli Pietiläinen, Aarno Palotie, Mark J Daly
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability. European journal of human genetics : EJHG 32 (5) (2024)
Lea Urpa, Mitja I Kurki, Elisa J Rahikkala, Eija Hämäläinen, Veikko V Salomaa, Jaana Suvisaari, Riikka Keski-Filppula, Merja Rauhala, Satu Korpi-Heikkilä, Jonna Komulainen-Ebrahim, Heli Helander, Päivi M Vieira, Johanna Uusimaa, Jukka S Moilanen, Jarmo Körkkö, Tarjinder Singh, Outi Kuismin, Olli Pietiläinen, Aarno Palotie, Mark J Daly
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability. European journal of human genetics : EJHG (2024)
Lea Urpa, Mitja I Kurki, Elisa J Rahikkala, Eija Hämäläinen, Veikko V Salomaa, Jaana Suvisaari, Riikka Keski-Filppula, Merja Rauhala, Satu Korpi-Heikkilä, Jonna Komulainen-Ebrahim, Heli Helander, Päivi M Vieira, Johanna Uusimaa, Jukka S Moilanen, Jarmo Körkkö, Tarjinder Singh, Outi Kuismin, Olli Pietiläinen, Aarno Palotie, Mark J Daly
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability. European journal of human genetics : EJHG 32 (5) (2024)
Lea Urpa, Mitja I Kurki, Elisa J Rahikkala, Eija Hämäläinen, Veikko V Salomaa, Jaana Suvisaari, Riikka Keski-Filppula, Merja Rauhala, Satu Korpi-Heikkilä, Jonna Komulainen-Ebrahim, Heli Helander, Päivi M Vieira, Johanna Uusimaa, Jukka S Moilanen, Jarmo Körkkö, Tarjinder Singh, Outi Kuismin, Olli Pietiläinen, Aarno Palotie, Mark J Daly
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability. European journal of human genetics : EJHG 32 (5) (2024)
Lea Urpa, Mitja I Kurki, Elisa J Rahikkala, Eija Hämäläinen, Veikko V Salomaa, Jaana Suvisaari, Riikka Keski-Filppula, Merja Rauhala, Satu Korpi-Heikkilä, Jonna Komulainen-Ebrahim, Heli Helander, Päivi M Vieira, Johanna Uusimaa, Jukka S Moilanen, Jarmo Körkkö, Tarjinder Singh, Outi Kuismin, Olli Pietiläinen, Aarno Palotie, Mark J Daly
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability. European journal of human genetics : EJHG 32 (5) (2024)
Eucharist Kun, Emily M Javan, Olivia Smith, Faris F Gulamali, Javier De la Fuente, Brianna I Flynn, Kushal Vajrala, Zoe D Trutner, Prakash Jayakumar, Elliot M Tucker-Drob, Mashaal Sohail, Tarjinder Singh, Vagheesh M Narasimhan
The genetic architecture of the human skeletal form. bioRxiv : the preprint server for biology (2023)
Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica S Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, null null, Katherine E Burdick, Joseph D Buxbaum, Enrico Domenici, Sophia Frangou, Annette M Hartmann, Claudine Laurent-Levinson, Dheeraj Malhotra, Carlos N Pato, Michele T Pato, Kerry James Ressler, Panagiotis Roussos, Dan Rujescu, Celso Arango, Alessandro Bertolino, Giuseppe Blasi, Luisella Bocchio-Chiavetto, Dominique Campion, Vaughan J Carr, Janice M Fullerton, Massimo Gennarelli, Javier González-Peñas, Douglas F Levinson, Bryan Mowry, Vishwajit L Nimgaokar, Giulio Pergola, Antonio Rampino, Jorge A Cervilla, Margarita Rivera, Sibylle G Schwab, Dieter B Wildenauer, Mark Daly, Benjamin M Neale, Tarjinder Singh, Michael C O'Donovan, Michael J Owen, James T R Walters, Muhammad Ayub, Anil K Malhotra, Todd Lencz, Patrick F Sullivan, Pamela Sklar, Eli A Stahl, Laura M Huckins, Alexander W Charney
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature genetics 55 (3) (2023)
Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica S Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, null null, Katherine E Burdick, Joseph D Buxbaum, Enrico Domenici, Sophia Frangou, Annette M Hartmann, Claudine Laurent-Levinson, Dheeraj Malhotra, Carlos N Pato, Michele T Pato, Kerry James Ressler, Panagiotis Roussos, Dan Rujescu, Celso Arango, Alessandro Bertolino, Giuseppe Blasi, Luisella Bocchio-Chiavetto, Dominique Campion, Vaughan J Carr, Janice M Fullerton, Massimo Gennarelli, Javier González-Peñas, Douglas F Levinson, Bryan Mowry, Vishwajit L Nimgaokar, Giulio Pergola, Antonio Rampino, Jorge A Cervilla, Margarita Rivera, Sibylle G Schwab, Dieter B Wildenauer, Mark Daly, Benjamin M Neale, Tarjinder Singh, Michael C O'Donovan, Michael J Owen, James T R Walters, Muhammad Ayub, Anil K Malhotra, Todd Lencz, Patrick F Sullivan, Pamela Sklar, Eli A Stahl, Laura M Huckins, Alexander W Charney
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature genetics 55 (3) (2023)
Eucharist Kun, Emily M Javan, Olivia Smith, Faris F Gulamali, Javier De la Fuente, Brianna I Flynn, Kushal Vajrala, Zoe D Trutner, Prakash Jayakumar, Elliot M Tucker-Drob, Mashaal Sohail, Tarjinder Singh, Vagheesh M Narasimhan
The genetic architecture of the human skeletal form. bioRxiv : the preprint server for biology (2023)
Chia-Yen Chen, Ruoyu Tian, Tian Ge, Max Lam, Gabriela Sanchez-Andrade, Tarjinder Singh, Lea Urpa, Jimmy Z Liu, Mark Sanderson, Christine Rowley, Holly Ironfield, Terry Fang, null null, null null, null null, Mark Daly, Aarno Palotie, Ellen A Tsai, Hailiang Huang, Matthew E Hurles, Sebastian S Gerety, Todd Lencz, Heiko Runz
The impact of rare protein coding genetic variation on adult cognitive function. Nature genetics (2023)
Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica S Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, null null, Katherine E Burdick, Joseph D Buxbaum, Enrico Domenici, Sophia Frangou, Annette M Hartmann, Claudine Laurent-Levinson, Dheeraj Malhotra, Carlos N Pato, Michele T Pato, Kerry James Ressler, Panagiotis Roussos, Dan Rujescu, Celso Arango, Alessandro Bertolino, Giuseppe Blasi, Luisella Bocchio-Chiavetto, Dominique Campion, Vaughan J Carr, Janice M Fullerton, Massimo Gennarelli, Javier González-Peñas, Douglas F Levinson, Bryan Mowry, Vishwajit L Nimgaokar, Giulio Pergola, Antonio Rampino, Jorge A Cervilla, Margarita Rivera, Sibylle G Schwab, Dieter B Wildenauer, Mark Daly, Benjamin M Neale, Tarjinder Singh, Michael C O'Donovan, Michael J Owen, James T R Walters, Muhammad Ayub, Anil K Malhotra, Todd Lencz, Patrick F Sullivan, Pamela Sklar, Eli A Stahl, Laura M Huckins, Alexander W Charney
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature genetics 55 (3) (2023)
Eucharist Kun, Emily M Javan, Olivia Smith, Faris F Gulamali, Javier De la Fuente, Brianna I Flynn, Kushal Vajrala, Zoe D Trutner, Prakash Jayakumar, Elliot M Tucker-Drob, Mashaal Sohail, Tarjinder Singh, Vagheesh M Narasimhan
The genetic architecture and evolution of the human skeletal form. Science (New York, N.Y.) 381 (6655) (2023)
Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica S Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, null null, Katherine E Burdick, Joseph D Buxbaum, Enrico Domenici, Sophia Frangou, Annette M Hartmann, Claudine Laurent-Levinson, Dheeraj Malhotra, Carlos N Pato, Michele T Pato, Kerry James Ressler, Panagiotis Roussos, Dan Rujescu, Celso Arango, Alessandro Bertolino, Giuseppe Blasi, Luisella Bocchio-Chiavetto, Dominique Campion, Vaughan J Carr, Janice M Fullerton, Massimo Gennarelli, Javier González-Peñas, Douglas F Levinson, Bryan Mowry, Vishwajit L Nimgaokar, Giulio Pergola, Antonio Rampino, Jorge A Cervilla, Margarita Rivera, Sibylle G Schwab, Dieter B Wildenauer, Mark Daly, Benjamin M Neale, Tarjinder Singh, Michael C O'Donovan, Michael J Owen, James T R Walters, Muhammad Ayub, Anil K Malhotra, Todd Lencz, Patrick F Sullivan, Pamela Sklar, Eli A Stahl, Laura M Huckins, Alexander W Charney
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations. Nature genetics 55 (3) (2023)
Eucharist Kun, Emily M Javan, Olivia Smith, Faris F Gulamali, Javier De la Fuente, Brianna I Flynn, Kushal Vajrala, Zoe D Trutner, Prakash Jayakumar, Elliot M Tucker-Drob, Mashaal Sohail, Tarjinder Singh, Vagheesh M Narasimhan
The genetic architecture of the human skeletal form. bioRxiv : the preprint server for biology (2023)
Borislav Dejanovic, Tiffany Wu, Ming-Chi Tsai, David Graykowski, Vineela D Gandham, Christopher M Rose, Corey E Bakalarski, Hai Ngu, Yuanyuan Wang, Shristi Pandey, Mitchell G Rezzonico, Brad A Friedman, Rose Edmonds, Ann De Mazière, Raphael Rakosi-Schmidt, Tarjinder Singh, Judith Klumperman, Oded Foreman, Michael C Chang, Luke Xie, Morgan Sheng, Jesse E Hanson
Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer's disease mouse models. Nature aging 2 (9) (2022)
Borislav Dejanovic, Tiffany Wu, Ming-Chi Tsai, David Graykowski, Vineela D Gandham, Christopher M Rose, Corey E Bakalarski, Hai Ngu, Yuanyuan Wang, Shristi Pandey, Mitchell G Rezzonico, Brad A Friedman, Rose Edmonds, Ann De Mazière, Raphael Rakosi-Schmidt, Tarjinder Singh, Judith Klumperman, Oded Foreman, Michael C Chang, Luke Xie, Morgan Sheng, Jesse E Hanson
Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer's disease mouse models. Nature aging 2 (9) (2022)
Borislav Dejanovic, Tiffany Wu, Ming-Chi Tsai, David Graykowski, Vineela D Gandham, Christopher M Rose, Corey E Bakalarski, Hai Ngu, Yuanyuan Wang, Shristi Pandey, Mitchell G Rezzonico, Brad A Friedman, Rose Edmonds, Ann De Mazière, Raphael Rakosi-Schmidt, Tarjinder Singh, Judith Klumperman, Oded Foreman, Michael C Chang, Luke Xie, Morgan Sheng, Jesse E Hanson
Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer's disease mouse models. Nature aging 2 (9) (2022)
Borislav Dejanovic, Tiffany Wu, Ming-Chi Tsai, David Graykowski, Vineela D Gandham, Christopher M Rose, Corey E Bakalarski, Hai Ngu, Yuanyuan Wang, Shristi Pandey, Mitchell G Rezzonico, Brad A Friedman, Rose Edmonds, Ann De Mazière, Raphael Rakosi-Schmidt, Tarjinder Singh, Judith Klumperman, Oded Foreman, Michael C Chang, Luke Xie, Morgan Sheng, Jesse E Hanson
Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer's disease mouse models. Nature aging 2 (9) (2022)
Tarjinder Singh, Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D Barchas, Nicholas Bass, Tim B Bigdeli, Gerome Breen, Evelyn J Bromet, Peter F Buckley, William E Bunney, Jonas Bybjerg-Grauholm, William F Byerley, Sinéad B Chapman, Wei J Chen, Claire Churchhouse, Nicholas Craddock, Caroline M Cusick, Lynn DeLisi, Sheila Dodge, Michael A Escamilla, Saana Eskelinen, Ayman H Fanous, Stephen V Faraone, Alessia Fiorentino, Laurent Francioli, Stacey B Gabriel, Diane Gage, Sarah A Gagliano Taliun, Andrea Ganna, Giulio Genovese, David C Glahn, Jakob Grove, Mei-Hua Hall, Eija Hämäläinen, Henrike O Heyne, Matti Holi, David M Hougaard, Daniel P Howrigan, Hailiang Huang, Hai-Gwo Hwu, René S Kahn, Hyun Min Kang, Konrad J Karczewski, George Kirov, James A Knowles, Francis S Lee, Douglas S Lehrer, Francesco Lescai, Dolores Malaspina, Stephen R Marder, Steven A McCarroll, Andrew M McIntosh, Helena Medeiros, Lili Milani, Christopher P Morley, Derek W Morris, Preben Bo Mortensen, Richard M Myers, Merete Nordentoft, Niamh L O'Brien, Ana Maria Olivares, Dost Ongur, Willem H Ouwehand, Duncan S Palmer, Tiina Paunio, Digby Quested, Mark H Rapaport, Elliott Rees, Brandi Rollins, F Kyle Satterstrom, Alan Schatzberg, Edward Scolnick, Laura J Scott, Sally I Sharp, Pamela Sklar, Jordan W Smoller, Janet L Sobell, Matthew Solomonson, Eli A Stahl, Christine R Stevens, Jaana Suvisaari, Grace Tiao, Stanley J Watson, Nicholas A Watts, Douglas H Blackwood, Anders D Børglum, Bruce M Cohen, Aiden P Corvin, Tõnu Esko, Nelson B Freimer, Stephen J Glatt, Christina M Hultman, Andrew McQuillin, Aarno Palotie, Carlos N Pato, Michele T Pato, Ann E Pulver, David St Clair, Ming T Tsuang, Marquis P Vawter, James T Walters, Thomas M Werge, Roel A Ophoff, Patrick F Sullivan, Michael J Owen, Michael Boehnke, Michael C O'Donovan, Benjamin M Neale, Mark J Daly
Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature 604 (7906) (2022)
Borislav Dejanovic, Tiffany Wu, Ming-Chi Tsai, David Graykowski, Vineela D Gandham, Christopher M Rose, Corey E Bakalarski, Hai Ngu, Yuanyuan Wang, Shristi Pandey, Mitchell G Rezzonico, Brad A Friedman, Rose Edmonds, Ann De Mazière, Raphael Rakosi-Schmidt, Tarjinder Singh, Judith Klumperman, Oded Foreman, Michael C Chang, Luke Xie, Morgan Sheng, Jesse E Hanson
Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer's disease mouse models. Nature aging 2 (9) (2022)
Duncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, Rolf Adolfsson, Nick Bass, Douglas H R Blackwood, Marco P M Boks, Chia-Yen Chen, Claire Churchhouse, Aiden P Corvin, Nicholas Craddock, David Curtis, Arianna Di Florio, Faith Dickerson, Nelson A Freimer, Fernando S Goes, Xiaoming Jia, Ian R Jones, Lisa A Jones, Lina Jonsson, Rene S Kahn, Mikaél Landén, Adam E Locke, Andrew M McIntosh, Andrew McQuillin, Derek W Morris, Michael C O'Donovan, Roel A Ophoff, Michael J Owen, Nancy L Pedersen, Danielle Posthuma, Andreas Reif, Neil Risch, Catherine Schaefer, Laura J Scott, Tarjinder Singh, Jordan W Smoller, Matthew Solomonson, David St Clair, Eli A Stahl, Annabel Vreeker, James T R Walters, Weiqing Wang, Nicholas A Watts, Robert Yolken, Peter P Zandi, Benjamin M Neale
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia. Nature genetics 54 (5) (2022)
Ralda Nehme, Olli Pietiläinen, Mykyta Artomov, Matthew Tegtmeyer, Vera Valakh, Leevi Lehtonen, Christina Bell, Tarjinder Singh, Aditi Trehan, John Sherwood, Danielle Manning, Emily R Peirent, Rhea Malik, Ellen J Guss, Derek Hawes, Amanda Beccard, Anne M Bara, Dane Z Hazelbaker, Emanuela Zuccaro, Giulio Genovese, Alexander A Loboda, Anna E Neumann, Christina Lilliehook, Outi Kuismin, Eija Hamalainen, Mitja Kurki, Christina M Hultman, Anna K Kähler, Joao A Paulo, Andrea Ganna, Jon Madison, Bruce M Cohen, Donna McPhie, Rolf Adolfsson, Roy Perlis, Ricardo Dolmetsch, Samouil L Farhi, Steven McCarroll, Steven Hyman, Benjamin M Neale, Lindy E Barrett, J Wade Harper, Aarno Palotie, Mark J Daly, Kevin C Eggan
The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia. Nature communications 13 (1) (2022)
Borislav Dejanovic, Tiffany Wu, Ming-Chi Tsai, David Graykowski, Vineela D Gandham, Christopher M Rose, Corey E Bakalarski, Hai Ngu, Yuanyuan Wang, Shristi Pandey, Mitchell G Rezzonico, Brad A Friedman, Rose Edmonds, Ann De Mazière, Raphael Rakosi-Schmidt, Tarjinder Singh, Judith Klumperman, Oded Foreman, Michael C Chang, Luke Xie, Morgan Sheng, Jesse E Hanson
Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer's disease mouse models. Nature aging 2 (9) (2022)
Daniel P Howrigan, Samuel A Rose, Kaitlin E Samocha, Menachem Fromer, Felecia Cerrato, Wei J Chen, Claire Churchhouse, Kimberly Chambert, Sharon D Chandler, Mark J Daly, Ashley Dumont, Giulio Genovese, Hai-Gwo Hwu, Nan Laird, Jack A Kosmicki, Jennifer L Moran, Cheryl Roe, Tarjinder Singh, Shi-Heng Wang, Stephen V Faraone, Stephen J Glatt, Steven A McCarroll, Ming T Tsuang, Benjamin M Neale
Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations. Nature neuroscience 23 (2) (2020)
Eugene J Gardner, Elena Prigmore, Giuseppe Gallone, Petr Danecek, Kaitlin E Samocha, Juliet Handsaker, Sebastian S Gerety, Holly Ironfield, Patrick J Short, Alejandro Sifrim, Tarjinder Singh, Kate E Chandler, Emma Clement, Katherine L Lachlan, Katrina Prescott, Elisabeth Rosser, David R FitzPatrick, Helen V Firth, Matthew E Hurles
Contribution of retrotransposition to developmental disorders. Nature communications 10 (1) (2019)
F Kyle Satterstrom, Raymond K Walters, Tarjinder Singh, Emilie M Wigdor, Francesco Lescai, Ditte Demontis, Jack A Kosmicki, Jakob Grove, Christine Stevens, Jonas Byberg-Grauholm, Marie Bækvad-Hansen, Duncan S Palmer, Julian B Maller, null null, Merete Nordentoft, Ole Mors, Elise B Robinson, David Michael Hougaard, Thomas M Werge, Preben Bo Mortensen, Benjamin M Neale, Anders Dupont Børglum, Mark J Daly
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants. Nature neuroscience 22 (12) (2019)
Henrike O Heyne, Tarjinder Singh, Hannah Stamberger, Rami Abou Jamra, Hande Caglayan, Dana Craiu, Peter De Jonghe, Renzo Guerrini, Katherine L Helbig, Bobby P C Koeleman, Jack A Kosmicki, Tarja Linnankivi, Patrick May, Hiltrud Muhle, Rikke S Møller, Bernd A Neubauer, Aarno Palotie, Manuela Pendziwiat, Pasquale Striano, Sha Tang, Sitao Wu, null null, Annapurna Poduri, Yvonne G Weber, Sarah Weckhuysen, Sanjay M Sisodiya, Mark J Daly, Ingo Helbig, Dennis Lal, Johannes R Lemke
De novo variants in neurodevelopmental disorders with epilepsy. Nature genetics 50 (7) (2018)

Tarjinder Singh.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Tarjinder Singh