Laura M Huckins (Laura Huckins)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 28

Top Venues

Nature genetics

Science (New York, N.Y.)

Molecular psychiatry

Nature neuroscience

Icahn School of Medicine at Mount Sinai

University of Cambridge (PHD)

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

Affiliation History

Icahn School of Medicine at Mount Sinai Nov 15o 2017

United States

Assistant Professor :: Pamela Sklar Division of Psychiatric Genomics

Education History

University of Cambridge Oct 3o 2011 - Nov 16o 2015

United Kingdom

PHD :: Human Genetics

Publications

Caleb J Browne, Rita Futamura, Angélica Minier-Toribio, Emily M Hicks, Aarthi Ramakrishnan, Freddyson J Martínez-Rivera, Molly Estill, Arthur Godino, Eric M Parise, Angelica Torres-Berrio, Ashley M Cunningham, Peter J Hamilton, Deena M Walker, Laura M Huckins, Yasmin L Hurd, Li Shen, Eric J Nestler
Transcriptional signatures of heroin intake and relapse throughout the brain reward circuitry in male mice. Science advances 9 (23) (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)
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, BaDoi N Phan, Xue Li, Diane P Genereux, Michael X Dong, Matteo Bianchi, Gregory Andrews, Sharadha Sakthikumar, Jessika Nordin, Ananya Roy, Matthew J Christmas, Voichita D Marinescu, Chao Wang, Ola Wallerman, James R Xue, Shuyang Yao, Quan Sun, Jin P Szatkiewicz, Jia Wen, Laura M Huckins, Alyssa J Lawler, Kathleen C Keough, Zhili Zheng, Jian Zeng, Naomi R Wray, Yun Li, Jessica S Johnson, Jiawen Chen, null null, Benedict Paten, Steven K Reilly, Graham M Hughes, Nishigandha Phalke, Katherine S Pollard, Andreas R Pfenning, Karin Forsberg-Nilsson, Elinor K Karlsson, Kerstin Lindblad-Toh, Gregory Andrews, Joel C Armstrong, Matteo Bianchi, Bruce W Birren, Kevin R Bredemeyer, Ana M Breit, Matthew J Christmas, Hiram Clawson, Joana Damas, Federica Di Palma, Mark Diekhans, Michael X Dong, Eduardo Eizirik, Kaili Fan, Cornelia Fanter, Nicole M Foley, Karin Forsberg-Nilsson, Carlos J Garcia, John Gatesy, Steven Gazal, Diane P Genereux, Linda Goodman, Jenna Grimshaw, Michaela K Halsey, Andrew J Harris, Glenn Hickey, Michael Hiller, Allyson G Hindle, Robert M Hubley, Graham M Hughes, Jeremy Johnson, David Juan, Irene M Kaplow, Elinor K Karlsson, Kathleen C Keough, Bogdan Kirilenko, Klaus-Peter Koepfli, Jennifer M Korstian, Amanda Kowalczyk, Sergey V Kozyrev, Alyssa J Lawler, Colleen Lawless, Thomas Lehmann, Danielle L Levesque, Harris A Lewin, Xue Li, Abigail Lind, Kerstin Lindblad-Toh, Ava Mackay-Smith, Voichita D Marinescu, Tomas Marques-Bonet, Victor C Mason, Jennifer R S Meadows, Wynn K Meyer, Jill E Moore, Lucas R Moreira, Diana D Moreno-Santillan, Kathleen M Morrill, Gerard Muntané, William J Murphy, Arcadi Navarro, Martin Nweeia, Sylvia Ortmann, Austin Osmanski, Benedict Paten, Nicole S Paulat, Andreas R Pfenning, BaDoi N Phan, Katherine S Pollard, Henry E Pratt, David A Ray, Steven K Reilly, Jeb R Rosen, Irina Ruf, Louise Ryan, Oliver A Ryder, Pardis C Sabeti, Daniel E Schäffer, Aitor Serres, Beth Shapiro, Arian F A Smit, Mark Springer, Chaitanya Srinivasan, Cynthia Steiner, Jessica M Storer, Kevin A M Sullivan, Patrick F Sullivan, Elisabeth Sundström, Megan A Supple, Ross Swofford, Joy-El Talbot, Emma Teeling, Jason Turner-Maier, Alejandro Valenzuela, Franziska Wagner, Ola Wallerman, Chao Wang, Juehan Wang, Zhiping Weng, Aryn P Wilder, Morgan E Wirthlin, James R Xue, Xiaomeng Zhang
Leveraging base-pair mammalian constraint to understand genetic variation and human disease. Science (New York, N.Y.) 380 (6643) (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)
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, BaDoi N Phan, Xue Li, Diane P Genereux, Michael X Dong, Matteo Bianchi, Gregory Andrews, Sharadha Sakthikumar, Jessika Nordin, Ananya Roy, Matthew J Christmas, Voichita D Marinescu, Chao Wang, Ola Wallerman, James R Xue, Shuyang Yao, Quan Sun, Jin P Szatkiewicz, Jia Wen, Laura M Huckins, Alyssa J Lawler, Kathleen C Keough, Zhili Zheng, Jian Zeng, Naomi R Wray, Yun Li, Jessica S Johnson, Jiawen Chen, null null, Benedict Paten, Steven K Reilly, Graham M Hughes, Nishigandha Phalke, Katherine S Pollard, Andreas R Pfenning, Karin Forsberg-Nilsson, Elinor K Karlsson, Kerstin Lindblad-Toh, Gregory Andrews, Joel C Armstrong, Matteo Bianchi, Bruce W Birren, Kevin R Bredemeyer, Ana M Breit, Matthew J Christmas, Hiram Clawson, Joana Damas, Federica Di Palma, Mark Diekhans, Michael X Dong, Eduardo Eizirik, Kaili Fan, Cornelia Fanter, Nicole M Foley, Karin Forsberg-Nilsson, Carlos J Garcia, John Gatesy, Steven Gazal, Diane P Genereux, Linda Goodman, Jenna Grimshaw, Michaela K Halsey, Andrew J Harris, Glenn Hickey, Michael Hiller, Allyson G Hindle, Robert M Hubley, Graham M Hughes, Jeremy Johnson, David Juan, Irene M Kaplow, Elinor K Karlsson, Kathleen C Keough, Bogdan Kirilenko, Klaus-Peter Koepfli, Jennifer M Korstian, Amanda Kowalczyk, Sergey V Kozyrev, Alyssa J Lawler, Colleen Lawless, Thomas Lehmann, Danielle L Levesque, Harris A Lewin, Xue Li, Abigail Lind, Kerstin Lindblad-Toh, Ava Mackay-Smith, Voichita D Marinescu, Tomas Marques-Bonet, Victor C Mason, Jennifer R S Meadows, Wynn K Meyer, Jill E Moore, Lucas R Moreira, Diana D Moreno-Santillan, Kathleen M Morrill, Gerard Muntané, William J Murphy, Arcadi Navarro, Martin Nweeia, Sylvia Ortmann, Austin Osmanski, Benedict Paten, Nicole S Paulat, Andreas R Pfenning, BaDoi N Phan, Katherine S Pollard, Henry E Pratt, David A Ray, Steven K Reilly, Jeb R Rosen, Irina Ruf, Louise Ryan, Oliver A Ryder, Pardis C Sabeti, Daniel E Schäffer, Aitor Serres, Beth Shapiro, Arian F A Smit, Mark Springer, Chaitanya Srinivasan, Cynthia Steiner, Jessica M Storer, Kevin A M Sullivan, Patrick F Sullivan, Elisabeth Sundström, Megan A Supple, Ross Swofford, Joy-El Talbot, Emma Teeling, Jason Turner-Maier, Alejandro Valenzuela, Franziska Wagner, Ola Wallerman, Chao Wang, Juehan Wang, Zhiping Weng, Aryn P Wilder, Morgan E Wirthlin, James R Xue, Xiaomeng Zhang
Leveraging base-pair mammalian constraint to understand genetic variation and human disease. Science (New York, N.Y.) 380 (6643) (2023)
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, BaDoi N Phan, Xue Li, Diane P Genereux, Michael X Dong, Matteo Bianchi, Gregory Andrews, Sharadha Sakthikumar, Jessika Nordin, Ananya Roy, Matthew J Christmas, Voichita D Marinescu, Chao Wang, Ola Wallerman, James R Xue, Shuyang Yao, Quan Sun, Jin P Szatkiewicz, Jia Wen, Laura M Huckins, Alyssa J Lawler, Kathleen C Keough, Zhili Zheng, Jian Zeng, Naomi R Wray, Yun Li, Jessica S Johnson, Jiawen Chen, null null, Benedict Paten, Steven K Reilly, Graham M Hughes, Nishigandha Phalke, Katherine S Pollard, Andreas R Pfenning, Karin Forsberg-Nilsson, Elinor K Karlsson, Kerstin Lindblad-Toh, Gregory Andrews, Joel C Armstrong, Matteo Bianchi, Bruce W Birren, Kevin R Bredemeyer, Ana M Breit, Matthew J Christmas, Hiram Clawson, Joana Damas, Federica Di Palma, Mark Diekhans, Michael X Dong, Eduardo Eizirik, Kaili Fan, Cornelia Fanter, Nicole M Foley, Karin Forsberg-Nilsson, Carlos J Garcia, John Gatesy, Steven Gazal, Diane P Genereux, Linda Goodman, Jenna Grimshaw, Michaela K Halsey, Andrew J Harris, Glenn Hickey, Michael Hiller, Allyson G Hindle, Robert M Hubley, Graham M Hughes, Jeremy Johnson, David Juan, Irene M Kaplow, Elinor K Karlsson, Kathleen C Keough, Bogdan Kirilenko, Klaus-Peter Koepfli, Jennifer M Korstian, Amanda Kowalczyk, Sergey V Kozyrev, Alyssa J Lawler, Colleen Lawless, Thomas Lehmann, Danielle L Levesque, Harris A Lewin, Xue Li, Abigail Lind, Kerstin Lindblad-Toh, Ava Mackay-Smith, Voichita D Marinescu, Tomas Marques-Bonet, Victor C Mason, Jennifer R S Meadows, Wynn K Meyer, Jill E Moore, Lucas R Moreira, Diana D Moreno-Santillan, Kathleen M Morrill, Gerard Muntané, William J Murphy, Arcadi Navarro, Martin Nweeia, Sylvia Ortmann, Austin Osmanski, Benedict Paten, Nicole S Paulat, Andreas R Pfenning, BaDoi N Phan, Katherine S Pollard, Henry E Pratt, David A Ray, Steven K Reilly, Jeb R Rosen, Irina Ruf, Louise Ryan, Oliver A Ryder, Pardis C Sabeti, Daniel E Schäffer, Aitor Serres, Beth Shapiro, Arian F A Smit, Mark Springer, Chaitanya Srinivasan, Cynthia Steiner, Jessica M Storer, Kevin A M Sullivan, Patrick F Sullivan, Elisabeth Sundström, Megan A Supple, Ross Swofford, Joy-El Talbot, Emma Teeling, Jason Turner-Maier, Alejandro Valenzuela, Franziska Wagner, Ola Wallerman, Chao Wang, Juehan Wang, Zhiping Weng, Aryn P Wilder, Morgan E Wirthlin, James R Xue, Xiaomeng Zhang
Leveraging base-pair mammalian constraint to understand genetic variation and human disease. Science (New York, N.Y.) 380 (6643) (2023)
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, BaDoi N Phan, Xue Li, Diane P Genereux, Michael X Dong, Matteo Bianchi, Gregory Andrews, Sharadha Sakthikumar, Jessika Nordin, Ananya Roy, Matthew J Christmas, Voichita D Marinescu, Chao Wang, Ola Wallerman, James R Xue, Shuyang Yao, Quan Sun, Jin P Szatkiewicz, Jia Wen, Laura M Huckins, Alyssa J Lawler, Kathleen C Keough, Zhili Zheng, Jian Zeng, Naomi R Wray, Yun Li, Jessica S Johnson, Jiawen Chen, null null, Benedict Paten, Steven K Reilly, Graham M Hughes, Nishigandha Phalke, Katherine S Pollard, Andreas R Pfenning, Karin Forsberg-Nilsson, Elinor K Karlsson, Kerstin Lindblad-Toh, Gregory Andrews, Joel C Armstrong, Matteo Bianchi, Bruce W Birren, Kevin R Bredemeyer, Ana M Breit, Matthew J Christmas, Hiram Clawson, Joana Damas, Federica Di Palma, Mark Diekhans, Michael X Dong, Eduardo Eizirik, Kaili Fan, Cornelia Fanter, Nicole M Foley, Karin Forsberg-Nilsson, Carlos J Garcia, John Gatesy, Steven Gazal, Diane P Genereux, Linda Goodman, Jenna Grimshaw, Michaela K Halsey, Andrew J Harris, Glenn Hickey, Michael Hiller, Allyson G Hindle, Robert M Hubley, Graham M Hughes, Jeremy Johnson, David Juan, Irene M Kaplow, Elinor K Karlsson, Kathleen C Keough, Bogdan Kirilenko, Klaus-Peter Koepfli, Jennifer M Korstian, Amanda Kowalczyk, Sergey V Kozyrev, Alyssa J Lawler, Colleen Lawless, Thomas Lehmann, Danielle L Levesque, Harris A Lewin, Xue Li, Abigail Lind, Kerstin Lindblad-Toh, Ava Mackay-Smith, Voichita D Marinescu, Tomas Marques-Bonet, Victor C Mason, Jennifer R S Meadows, Wynn K Meyer, Jill E Moore, Lucas R Moreira, Diana D Moreno-Santillan, Kathleen M Morrill, Gerard Muntané, William J Murphy, Arcadi Navarro, Martin Nweeia, Sylvia Ortmann, Austin Osmanski, Benedict Paten, Nicole S Paulat, Andreas R Pfenning, BaDoi N Phan, Katherine S Pollard, Henry E Pratt, David A Ray, Steven K Reilly, Jeb R Rosen, Irina Ruf, Louise Ryan, Oliver A Ryder, Pardis C Sabeti, Daniel E Schäffer, Aitor Serres, Beth Shapiro, Arian F A Smit, Mark Springer, Chaitanya Srinivasan, Cynthia Steiner, Jessica M Storer, Kevin A M Sullivan, Patrick F Sullivan, Elisabeth Sundström, Megan A Supple, Ross Swofford, Joy-El Talbot, Emma Teeling, Jason Turner-Maier, Alejandro Valenzuela, Franziska Wagner, Ola Wallerman, Chao Wang, Juehan Wang, Zhiping Weng, Aryn P Wilder, Morgan E Wirthlin, James R Xue, Xiaomeng Zhang
Leveraging base-pair mammalian constraint to understand genetic variation and human disease. Science (New York, N.Y.) 380 (6643) (2023)
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, BaDoi N Phan, Xue Li, Diane P Genereux, Michael X Dong, Matteo Bianchi, Gregory Andrews, Sharadha Sakthikumar, Jessika Nordin, Ananya Roy, Matthew J Christmas, Voichita D Marinescu, Chao Wang, Ola Wallerman, James R Xue, Shuyang Yao, Quan Sun, Jin P Szatkiewicz, Jia Wen, Laura M Huckins, Alyssa J Lawler, Kathleen C Keough, Zhili Zheng, Jian Zeng, Naomi R Wray, Yun Li, Jessica S Johnson, Jiawen Chen, null null, Benedict Paten, Steven K Reilly, Graham M Hughes, Nishigandha Phalke, Katherine S Pollard, Andreas R Pfenning, Karin Forsberg-Nilsson, Elinor K Karlsson, Kerstin Lindblad-Toh
Leveraging base-pair mammalian constraint to understand genetic variation and human disease. Science (New York, N.Y.) 380 (6643) (2023)
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, BaDoi N Phan, Xue Li, Diane P Genereux, Michael X Dong, Matteo Bianchi, Gregory Andrews, Sharadha Sakthikumar, Jessika Nordin, Ananya Roy, Matthew J Christmas, Voichita D Marinescu, Chao Wang, Ola Wallerman, James R Xue, Shuyang Yao, Quan Sun, Jin P Szatkiewicz, Jia Wen, Laura M Huckins, Alyssa J Lawler, Kathleen C Keough, Zhili Zheng, Jian Zeng, Naomi R Wray, Yun Li, Jessica S Johnson, Jiawen Chen, null null, Benedict Paten, Steven K Reilly, Graham M Hughes, Nishigandha Phalke, Katherine S Pollard, Andreas R Pfenning, Karin Forsberg-Nilsson, Elinor K Karlsson, Kerstin Lindblad-Toh
Leveraging base-pair mammalian constraint to understand genetic variation and human disease. Science (New York, N.Y.) 380 (6643) (2023)
Pj Michael Deans, Carina Seah, Jessica S Johnson, Judit Garcia Gonzalez, Kayla G Townsley, Evan Cao, Nadine Schrode, Eli A Stahl, Paul F O'Reilly, Laura M Huckins, Kristen J Brennand
Non-additive effects of schizophrenia risk genes reflect convergent downstream function. medRxiv : the preprint server for health sciences (2023)
Patrick F Sullivan, Jennifer R S Meadows, Steven Gazal, BaDoi N Phan, Xue Li, Diane P Genereux, Michael X Dong, Matteo Bianchi, Gregory Andrews, Sharadha Sakthikumar, Jessika Nordin, Ananya Roy, Matthew J Christmas, Voichita D Marinescu, Chao Wang, Ola Wallerman, James R Xue, Shuyang Yao, Quan Sun, Jin P Szatkiewicz, Jia Wen, Laura M Huckins, Alyssa J Lawler, Kathleen C Keough, Zhili Zheng, Jian Zeng, Naomi R Wray, Yun Li, Jessica S Johnson, Jiawen Chen, null null, Benedict Paten, Steven K Reilly, Graham M Hughes, Nishigandha Phalke, Katherine S Pollard, Andreas R Pfenning, Karin Forsberg-Nilsson, Elinor K Karlsson, Kerstin Lindblad-Toh, Gregory Andrews, Joel C Armstrong, Matteo Bianchi, Bruce W Birren, Kevin R Bredemeyer, Ana M Breit, Matthew J Christmas, Hiram Clawson, Joana Damas, Federica Di Palma, Mark Diekhans, Michael X Dong, Eduardo Eizirik, Kaili Fan, Cornelia Fanter, Nicole M Foley, Karin Forsberg-Nilsson, Carlos J Garcia, John Gatesy, Steven Gazal, Diane P Genereux, Linda Goodman, Jenna Grimshaw, Michaela K Halsey, Andrew J Harris, Glenn Hickey, Michael Hiller, Allyson G Hindle, Robert M Hubley, Graham M Hughes, Jeremy Johnson, David Juan, Irene M Kaplow, Elinor K Karlsson, Kathleen C Keough, Bogdan Kirilenko, Klaus-Peter Koepfli, Jennifer M Korstian, Amanda Kowalczyk, Sergey V Kozyrev, Alyssa J Lawler, Colleen Lawless, Thomas Lehmann, Danielle L Levesque, Harris A Lewin, Xue Li, Abigail Lind, Kerstin Lindblad-Toh, Ava Mackay-Smith, Voichita D Marinescu, Tomas Marques-Bonet, Victor C Mason, Jennifer R S Meadows, Wynn K Meyer, Jill E Moore, Lucas R Moreira, Diana D Moreno-Santillan, Kathleen M Morrill, Gerard Muntané, William J Murphy, Arcadi Navarro, Martin Nweeia, Sylvia Ortmann, Austin Osmanski, Benedict Paten, Nicole S Paulat, Andreas R Pfenning, BaDoi N Phan, Katherine S Pollard, Henry E Pratt, David A Ray, Steven K Reilly, Jeb R Rosen, Irina Ruf, Louise Ryan, Oliver A Ryder, Pardis C Sabeti, Daniel E Schäffer, Aitor Serres, Beth Shapiro, Arian F A Smit, Mark Springer, Chaitanya Srinivasan, Cynthia Steiner, Jessica M Storer, Kevin A M Sullivan, Patrick F Sullivan, Elisabeth Sundström, Megan A Supple, Ross Swofford, Joy-El Talbot, Emma Teeling, Jason Turner-Maier, Alejandro Valenzuela, Franziska Wagner, Ola Wallerman, Chao Wang, Juehan Wang, Zhiping Weng, Aryn P Wilder, Morgan E Wirthlin, James R Xue, Xiaomeng Zhang
Leveraging base-pair mammalian constraint to understand genetic variation and human disease. Science (New York, N.Y.) 380 (6643) (2023)
Laura M Huckins, Rebecca Signer, Jessica Johnson, Ya-Ke Wu, Karen S Mitchell, Cynthia M Bulik
What next for eating disorder genetics? Replacing myths with facts to sharpen our understanding. Molecular psychiatry 27 (10) (2022)
Jessica S Johnson, Alanna C Cote, Amanda Dobbyn, Laura G Sloofman, Jiayi Xu, Liam Cotter, Alexander W Charney, null null, Andreas Birgegård, Jennifer Jordan, Martin Alexander Kennedy, Mikaél Landén, Sarah L Maguire, Nicholas G Martin, Preben Bo Mortensen, Laura M Thornton, Cynthia M Bulik, Laura M Huckins
Mapping anorexia nervosa genes to clinical phenotypes. Psychological medicine (2022)
Shelby Marchese, Laura M Huckins
Trauma Matters: Integrating Genetic and Environmental Components of PTSD. Advanced genetics (Hoboken, N.J.) 4 (3) (2022)
Frank R Wendt, Gita A Pathak, Joseph D Deak, Flavio De Angelis, Dora Koller, Brenda Cabrera-Mendoza, Dannielle S Lebovitch, Daniel F Levey, Murray B Stein, Henry R Kranzler, Karestan C Koenen, Joel Gelernter, Laura M Huckins, Renato Polimanti
Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder. Molecular psychiatry 27 (4) (2022)
Alanna C Cote, Hannah E Young, Laura M Huckins
Comparison of confound adjustment methods in the construction of gene co-expression networks. Genome biology 23 (1) (2022)
Ryan C Thompson, Nicole W Simons, Lillian Wilkins, Esther Cheng, Diane M Del Valle, Gabriel E Hoffman, Carlo Cervia, Brian Fennessy, Konstantinos Mouskas, Nancy J Francoeur, Jessica S Johnson, Lauren Lepow, Jessica Le Berichel, Christie Chang, Aviva G Beckmann, Ying-Chih Wang, Kai Nie, Nicholas Zaki, Kevin Tuballes, Vanessa Barcessat, Mario A Cedillo, Dan Yuan, Laura M Huckins, Panagiotis Roussos, Thomas U Marron, null null, Benjamin Scott Glicksberg, Girish N Nadkarni, James R Heath, Edgar G Kozlova, Onur Boyman, Seunghee Kim-Schulze, Robert Sebra, Miriam Merad, Sacha Gnjatic, Eric E Schadt, Alexander W Charney, Noam D Beckmann
Molecular states during acute COVID-19 reveal distinct etiologies of long-term sequelae. Nature medicine (2022)
Shelby Marchese, Leo Cancelmo, Olivia Diab, Leah Cahn, Cindy Aaronson, Nikolaos P Daskalakis, Jamie Schaffer, Sarah R Horn, Jessica S Johnson, Clyde Schechter, Frank Desarnaud, Linda M Bierer, Iouri Makotkine, Janine D Flory, Michael Crane, Jacqueline M Moline, Iris G Udasin, Denise J Harrison, Panagiotis Roussos, Dennis S Charney, Karestan C Koenen, Steven M Southwick, Rachel Yehuda, Robert H Pietrzak, Laura M Huckins, Adriana Feder
Altered gene expression and PTSD symptom dimensions in World Trade Center responders. Molecular psychiatry 27 (4) (2022)
Carina Seah, Michael S Breen, Tom Rusielewicz, Heather N Bader, Changxin Xu, Christopher J Hunter, Barry McCarthy, P J Michael Deans, Mitali Chattopadhyay, Jordan Goldberg, Frank Desarnaud, Iouri Makotkine, Janine D Flory, Linda M Bierer, Migle Staniskyte, null null, Scott A Noggle, Laura M Huckins, Daniel Paull, Kristen J Brennand, Rachel Yehuda
Modeling gene × environment interactions in PTSD using human neurons reveals diagnosis-specific glucocorticoid-induced gene expression. Nature neuroscience 25 (11) (2022)
Samuel K Powell, Callan O'Shea, Kayla G Townsley, Iya Prytkova, Kristina Dobrindt, Rahat Elahi, Marina Iskhakova, Tova Y Lambert, Aditi Valada, Will Liao, Seok-Man Ho, Paul A Slesinger, Laura M Huckins, Schahram Akbarian, Kristen J Brennand
Induction of dopaminergic neurons for neuronal subtype-specific modeling of psychiatric disease risk. Molecular psychiatry (2021)
Akhil Vaid, Sulaiman S Somani, Adam J Russak, Jessica K De Freitas, Fayzan F Chaudhry, Ishan Paranjpe, Kipp W Johnson, Samuel J Lee, Riccardo Miotto, Felix Richter, Shan P Zhao, Noam D Beckmann, Nidhi Naik, Arash Kia, Prem Timsina, Anuradha Lala, Manish D Paranjpe, Eddye A Golden, Matteo Danieletto, Manbir Singh, Dara Meyer, Paul F O'Reilly, Laura M Huckins, Patricia Kovatch, Joseph Finkelstein, Robert M Freeman, Edgar Argulian, Andrew Kasarskis, Bethany L Percha, Judith A Aberg, Emilia Bagiella, Carol R Horowitz, Barbara Murphy, Eric J Nestler, Eric E Schadt, Judy H Cho, Carlos Cordon-Cardo, Valentin Fuster, Dennis S Charney, David L Reich, Erwin P Böttinger, Matthew A Levin, Jagat Narula, Zahi Adel Fayad, Allan Carpenter Just, Alexander W Charney, Girish N Nadkarni, Benjamin Scott Glicksberg
Machine Learning to Predict Mortality and Critical Events in a Cohort of Patients With COVID-19 in New York City: Model Development and Validation. Journal of medical Internet research 22 (11) (2020)
Kayla G Townsley, Kristen J Brennand, Laura M Huckins
Massively parallel techniques for cataloguing the regulome of the human brain. Nature neuroscience 23 (12) (2020)
Ditte Demontis, Veera Manikandan Rajagopal, Thorgeir E Thorgeirsson, Thomas Damm Als, Jakob Grove, Kalle Leppälä, Daníel F Guðbjartsson, Jonatan Pallesen, Carsten Rygaard Hjorthøj, Gunnar W Reginsson, Thorarinn Tyrfingsson, Valgerdur Runarsdottir, Per Qvist, Jane Hvarregaard Christensen, Jonas Byberg-Grauholm, Marie Bækvad-Hansen, Laura M Huckins, Eli A Stahl, Allan Timmermann, Esben Agerbo, David Michael Hougaard, Thomas M Werge, Ole Mors, Preben Bo Mortensen, Merete Nordentoft, Mark J Daly, Hreinn Stefánsson, Kári Stefánsson, Mette Nyegaard, Anders Dupont Børglum
Genome-wide association study implicates CHRNA2 in cannabis use disorder. Nature neuroscience 22 (7) (2019)
Laura M Huckins, Amanda Dobbyn, Douglas M Ruderfer, Gabriel E Hoffman, Weiqing Wang, Antonio F Pardinas, Veera Manikandan Rajagopal, Thomas Damm Als, Hoang T Nguyen, Kiran Girdhar, James Boocock, Panagiotis Roussos, Menachem Fromer, Robin Kramer, Enrico Domenici, Eric R Gamazon, Shaun M Purcell, null null, null null, null null, Ditte Demontis, Anders Dupont Børglum, James T R Walters, Michael C O'Donovan, Patrick F Sullivan, Michael J Owen, Bernie Devlin, Solveig K Sieberts, Nancy J Cox, Hae Kyung Im, Pamela Sklar, Eli A Stahl
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature genetics 51 (4) (2019)
Nadine Schrode, Seok-Man Ho, Kazuhiko Yamamuro, Amanda Dobbyn, Laura M Huckins, Marliette R Matos, Esther Cheng, P J Michael Deans, Erin Flaherty, Natalie Barretto, Aaron Topol, Khaled Alganem, Sonya Abadali, James Gregory, Emily Hoelzli, Hemali Phatnani, Vineeta Singh, Deeptha Girish, Bruce Aronow, Robert Mccullumsmith, Gabriel E Hoffman, Eli A Stahl, Hirofumi Morishita, Pamela Sklar, Kristen J Brennand
Synergistic effects of common schizophrenia risk variants. Nature genetics 51 (10) (2019)
Antonio F Pardinas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere, Jun Han, Leon Hubbard, Amy Joanne Lynham, Kiran Mantripragada, Elliott Rees, James Hunter MacCabe, Steven A McCarroll, Bernhard T Baune, Gerome D Breen, Enda M Byrne, Udo Dannlowski, Thalia C Eley, Caroline Hayward, Nicholas G Martin, Andrew M McIntosh, Robert Plomin, David J Porteous, Naomi R Wray, Armando Caballero, Daniel H Geschwind, Laura M Huckins, Douglas M Ruderfer, Enrique Santiago, Pamela Sklar, Eli A Stahl, Hyejung Won, Esben Agerbo, Thomas Damm Als, Ole A Andreassen, Marie Bækvad-Hansen, Preben Bo Mortensen, Carsten Bøcker Pedersen, Anders D Børglum, Jonas Byberg-Grauholm, Srdjan Djurovic, Naser Durmishi, Marianne Giørtz Pedersen, Vera Golimbet, Jakob Grove, David Michael Hougaard, Manuel Mattheisen, Espen Molden, Ole Mors, Merete Nordentoft, Milica Pejovic-Milovancevic, Engilbert Sigurdsson, Teimuraz Silagadze, Christine Søholm Hansen, Kari Stefansson, Hreinn Stefansson, Stacy Steinberg, Sarah Tosato, Thomas Werge, null null, null null, David A Collier, Dan Rujescu, George Kirov, Michael J Owen, Michael C O'Donovan, James T R Walters
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature genetics 50 (3) (2018)

Laura M Huckins.css-eqlu8i{font-size:small;padding-left:4px;} (Laura Huckins)

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Laura M Huckins (Laura Huckins)