Terrence Blaine Crowley (Terrence B Crowley, T B Crowley, T Blaine Crowley, T Blaine Crowley)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 37

Top Venues

Genes

American journal of medical genetics. Part A

Science (New York, N.Y.)

Molecular psychiatry

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

Publications

Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, Terrence Blaine Crowley, Valeria Capra, Jeremiah Martino, Meade Haller, Camila Araújo, Hélio R Machado, Renee George, Bryn Gerding, Kiely N James, Valentina Stanley, Nan Jiang, Kameron Alu, Naomi Meave, Anna S Nidhiry, Fiza Jiwani, Isaac Tang, Ashna Nisal, Ishani Jhamb, Arzoo Patel, Aakash Patel, Jennifer McEvoy-Venneri, Chelsea Barrows, Celina Shen, Yoo-Jin Ha, Robyn Howarth, Madison Strain, Allison Elizabeth Ashley-Koch, Matloob Azam, Sara Mumtaz, Gyang Markus Bot, Richard H Finnell, Zoha Kibar, Ahmed I Marwan, Gia Melikishvili, Hal S Meltzer, Osvaldo M Mutchinick, David A Stevenson, Henry J Mroczkowski, Betsy Ostrander, Erica Schindewolf, Julie Moldenhauer, Elaine H Zackai, Beverly S Emanuel, Sixto García-Miñaúr, Sebastian Kwiatkowski, Roger E Stevenson, Maha Saad Zaki, Hope Northrup, Hanna K McNamara, Kimberly A Aldinger, Ian G Phelps, Mei Deng, Ian A Glass, null null, Bernice E Morrow, Donna M McDonald-McGinn, Simone Sanna-Cherchi, Dolores J Lamb, Joseph G Gleeson
Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science (New York, N.Y.) 384 (6695) (2024)
Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart, Terrence Blaine Crowley, Stephanie Asher, Amanda Back, Sarah M Baldino, Emma Bedoukian, Allison D Britt, Natalie Burrill, Cara Cacioppo, Dana Farengo Clark, Mary Egan Clark, Laura Conway, Laynie Dratch, Holly A Dubbs, Nicole M Engelhardt, Natalie Ginn, Christopher Gray, Tiff Hartman, Evan R Hathaway, Katherine L Helbig, Lily Hoffman-Andrews, Stefanie Kasperski, Beth A Keena, Kierstin N Keller, Katherine L Nathanson, Lauren Lulis, Laina Lusk, Daniel E McGinn, Rebecca Mueller, Rache A Paul, Lisa Pilchman, Jacquelyn Powers, Sarah E Raible, Sara Reichert, Alyssa L Ritter, Angela G Arnold, Sarah M Ruggiero, Erica Schindewolf, Katie Rose Sullivan, Shannon Terek, Bekah Wang, McKenzie Wells, Natalia Wisniewski, Renee Wright, Elisabeth McCarty Wood, Stacy Woyciechowski, Kristin Zelley, Kathleen D Valverde, Donna M McDonald-McGinn
Expanding Genetic Counselor Roles: A Model for Global Research Development. Genes 15 (7) (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart, Terrence Blaine Crowley, Stephanie Asher, Amanda Back, Sarah M Baldino, Emma Bedoukian, Allison D Britt, Natalie Burrill, Cara Cacioppo, Dana Farengo Clark, Mary Egan Clark, Laura Conway, Laynie Dratch, Holly A Dubbs, Nicole M Engelhardt, Natalie Ginn, Christopher Gray, Tiff Hartman, Evan R Hathaway, Katherine L Helbig, Lily Hoffman-Andrews, Stefanie Kasperski, Beth A Keena, Kierstin N Keller, Katherine L Nathanson, Lauren Lulis, Laina Lusk, Daniel E McGinn, Rebecca Mueller, Rache A Paul, Lisa Pilchman, Jacquelyn Powers, Sarah E Raible, Sara Reichert, Alyssa L Ritter, Angela G Arnold, Sarah M Ruggiero, Erica Schindewolf, Katie Rose Sullivan, Shannon Terek, Bekah Wang, McKenzie Wells, Natalia Wisniewski, Renee Wright, Elisabeth McCarty Wood, Stacy Woyciechowski, Kristin Zelley, Kathleen D Valverde, Donna M McDonald-McGinn
Expanding Genetic Counselor Roles: A Model for Global Research Development. Genes 15 (7) (2024)
Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, Terrence Blaine Crowley, Valeria Capra, Jeremiah Martino, Meade Haller, Camila Araújo, Hélio R Machado, Renee George, Bryn Gerding, Kiely N James, Valentina Stanley, Nan Jiang, Kameron Alu, Naomi Meave, Anna S Nidhiry, Fiza Jiwani, Isaac Tang, Ashna Nisal, Ishani Jhamb, Arzoo Patel, Aakash Patel, Jennifer McEvoy-Venneri, Chelsea Barrows, Celina Shen, Yoo-Jin Ha, Robyn Howarth, Madison Strain, Allison Elizabeth Ashley-Koch, Matloob Azam, Sara Mumtaz, Gyang Markus Bot, Richard H Finnell, Zoha Kibar, Ahmed I Marwan, Gia Melikishvili, Hal S Meltzer, Osvaldo M Mutchinick, David A Stevenson, Henry J Mroczkowski, Betsy Ostrander, Erica Schindewolf, Julie Moldenhauer, Elaine H Zackai, Beverly S Emanuel, Sixto García-Miñaúr, Sebastian Kwiatkowski, Roger E Stevenson, Maha Saad Zaki, Hope Northrup, Hanna K McNamara, Kimberly A Aldinger, Ian G Phelps, Mei Deng, Ian A Glass, null null, Bernice E Morrow, Donna M McDonald-McGinn, Simone Sanna-Cherchi, Dolores J Lamb, Joseph G Gleeson, Allison Elizabeth Ashley Koch, Hal S Meltzer, Joan Le, Kit Sing Au, Hope Northrup, Gyang Markus Bot, Valeria Capra, Richard H Finnell, Zoha Kibar, Philip J Lupo, Helio R Machado, Camila Araújo, Tony Magana, Ahmed I Marwan, Gia Melikishvili, Osvaldo M Mutchinick, Roger E Stevenson, Anna Yurrita, Maha S Zaki, Sara Mumtaz, José Ramón Medina-Bereciartu, Caroline M Kolvenbach, Shirlee Shril, Friedhelm Hildebrandt, Mahmoud M Noureldeen, Aida Ms Salem, Yukitoshi Takahashi, Hormos Salimi-Dafsari, H Westley Phillips, Brian Hanak, Bülent Kara, Ayfer Sakarya Güneş, David D Gonda, Salman Kirmani, Tinatin Tkemaladze, Joseph G Gleeson
Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science (New York, N.Y.) 384 (6695) (2024)
Colleen C Muraresku, Elizabeth M McCormick, Lydia Rockart, Terrence Blaine Crowley, Stephanie Asher, Amanda Back, Sarah M Baldino, Emma Bedoukian, Allison D Britt, Natalie Burrill, Cara Cacioppo, Dana Farengo Clark, Mary Egan Clark, Laura Conway, Laynie Dratch, Holly A Dubbs, Nicole M Engelhardt, Natalie Ginn, Christopher Gray, Tiff Hartman, Evan R Hathaway, Katherine L Helbig, Lily Hoffman-Andrews, Stefanie Kasperski, Beth A Keena, Kierstin N Keller, Katherine L Nathanson, Lauren Lulis, Laina Lusk, Daniel E McGinn, Rebecca Mueller, Rache A Paul, Lisa Pilchman, Jacquelyn Powers, Sarah E Raible, Sara Reichert, Alyssa L Ritter, Angela G Arnold, Sarah M Ruggiero, Erica Schindewolf, Katie Rose Sullivan, Shannon Terek, Bekah Wang, McKenzie Wells, Natalia Wisniewski, Renee Wright, Elisabeth McCarty Wood, Stacy Woyciechowski, Kristin Zelley, Kathleen D Valverde, Donna M McDonald-McGinn
Expanding Genetic Counselor Roles: A Model for Global Research Development. Genes 15 (7) (2024)
Keng Ioi Vong, Sangmoon Lee, Kit Sing Au, Terrence Blaine Crowley, Valeria Capra, Jeremiah Martino, Meade Haller, Camila Araújo, Hélio R Machado, Renee George, Bryn Gerding, Kiely N James, Valentina Stanley, Nan Jiang, Kameron Alu, Naomi Meave, Anna S Nidhiry, Fiza Jiwani, Isaac Tang, Ashna Nisal, Ishani Jhamb, Arzoo Patel, Aakash Patel, Jennifer McEvoy-Venneri, Chelsea Barrows, Celina Shen, Yoo-Jin Ha, Robyn Howarth, Madison Strain, Allison Elizabeth Ashley-Koch, Matloob Azam, Sara Mumtaz, Gyang Markus Bot, Richard H Finnell, Zoha Kibar, Ahmed I Marwan, Gia Melikishvili, Hal S Meltzer, Osvaldo M Mutchinick, David A Stevenson, Henry J Mroczkowski, Betsy Ostrander, Erica Schindewolf, Julie Moldenhauer, Elaine H Zackai, Beverly S Emanuel, Sixto García-Miñaúr, Sebastian Kwiatkowski, Roger E Stevenson, Maha Saad Zaki, Hope Northrup, Hanna K McNamara, Kimberly A Aldinger, Ian G Phelps, Mei Deng, Ian A Glass, null null, Bernice E Morrow, Donna M McDonald-McGinn, Simone Sanna-Cherchi, Dolores J Lamb, Joseph G Gleeson
Risk of meningomyelocele mediated by the common 22q11.2 deletion. Science (New York, N.Y.) 384 (6695) (2024)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, Tomasz Gambin, Anna Kutkowska-Kaźmierczak, Katarzyna Kowalczyk, Izabela Plaskota, Barbara Wiśniowiecka-Kowalnik, Magdalena Bartnik-Głaska, Magdalena Niemiec, Dominika Grad, Małgorzata Piotrowicz, Dorota Gieruszczak-Białek, Aleksandra Pietrzyk, Terrence Blaine Crowley, Victoria Giunta, Daniel E McGinn, Elaine H Zackai, Oanh Tran, Beverly S Emanuel, Donna M McDonald-McGinn, Beata A Nowakowska
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome. Genes 14 (3) (2023)
Jente Verbesselt, Cynthia B Solot, Ellen Van Den Heuvel, Terrence Blaine Crowley, Victoria Giunta, Jeroen Breckpot, Donna M McDonald-McGinn, Inge Zink, Ann Swillen
Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants. Genes 14 (3) (2023)
Lauren K White, Terrence Blaine Crowley, Brenda Finucane, Emily J McClellan, Sarah Donoghue, Sixto Garcia-Minaur, Gabriela M Repetto, Matthias Fischer, Sebastien Jacquemont, Raquel E Gur, Anne Manuela Maillard, Kirsten Ann Donald, Anne Susan Bassett, Ann Swillen, Donna M McDonald-McGinn
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes 14 (1) (2023)
Lauren K White, Terrence Blaine Crowley, Brenda Finucane, Emily J McClellan, Sarah Donoghue, Sixto Garcia-Minaur, Gabriela M Repetto, Matthias Fischer, Sebastien Jacquemont, Raquel E Gur, Anne Manuela Maillard, Kirsten Ann Donald, Anne Susan Bassett, Ann Swillen, Donna M McDonald-McGinn
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes 14 (1) (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Lauren K White, Terrence Blaine Crowley, Brenda Finucane, Emily J McClellan, Sarah Donoghue, Sixto Garcia-Minaur, Gabriela M Repetto, Matthias Fischer, Sebastien Jacquemont, Raquel E Gur, Anne Manuela Maillard, Kirsten Ann Donald, Anne Susan Bassett, Ann Swillen, Donna M McDonald-McGinn
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes 14 (1) (2023)
Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, Tomasz Gambin, Anna Kutkowska-Kaźmierczak, Katarzyna Kowalczyk, Izabela Plaskota, Barbara Wiśniowiecka-Kowalnik, Magdalena Bartnik-Głaska, Magdalena Niemiec, Dominika Grad, Małgorzata Piotrowicz, Dorota Gieruszczak-Białek, Aleksandra Pietrzyk, Terrence Blaine Crowley, Victoria Giunta, Daniel E McGinn, Elaine H Zackai, Oanh Tran, Beverly S Emanuel, Donna M McDonald-McGinn, Beata A Nowakowska
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome. Genes 14 (3) (2023)
Marta Smyk, Maciej Geremek, Kamila Ziemkiewicz, Tomasz Gambin, Anna Kutkowska-Kaźmierczak, Katarzyna Kowalczyk, Izabela Plaskota, Barbara Wiśniowiecka-Kowalnik, Magdalena Bartnik-Głaska, Magdalena Niemiec, Dominika Grad, Małgorzata Piotrowicz, Dorota Gieruszczak-Białek, Aleksandra Pietrzyk, Terrence Blaine Crowley, Victoria Giunta, Daniel E McGinn, Elaine H Zackai, Oanh Tran, Beverly S Emanuel, Donna M McDonald-McGinn, Beata A Nowakowska
Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome. Genes 14 (3) (2023)
Jente Verbesselt, Cynthia B Solot, Ellen Van Den Heuvel, Terrence Blaine Crowley, Victoria Giunta, Jeroen Breckpot, Donna M McDonald-McGinn, Inge Zink, Ann Swillen
Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants. Genes 14 (3) (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Jente Verbesselt, Cynthia B Solot, Ellen Van Den Heuvel, Terrence Blaine Crowley, Victoria Giunta, Jeroen Breckpot, Donna M McDonald-McGinn, Inge Zink, Ann Swillen
Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants. Genes 14 (3) (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Hayley A Ron, Terrence Blaine Crowley, Yichuan Liu, Marta Unolt, Erica Schindewolf, Julie Moldenhauer, Jack Rychik, Elizabeth Goldmuntz, Beverly S Emanuel, Douglas Ryba, James William Gaynor, Elaine H Zackai, Hakon Hakonarson, Donna M McDonald-McGinn
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study. Genes 14 (1) (2022)
Hayley A Ron, Terrence Blaine Crowley, Yichuan Liu, Marta Unolt, Erica Schindewolf, Julie Moldenhauer, Jack Rychik, Elizabeth Goldmuntz, Beverly S Emanuel, Douglas Ryba, James William Gaynor, Elaine H Zackai, Hakon Hakonarson, Donna M McDonald-McGinn
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study. Genes 14 (1) (2022)
Hayley A Ron, Terrence Blaine Crowley, Yichuan Liu, Marta Unolt, Erica Schindewolf, Julie Moldenhauer, Jack Rychik, Elizabeth Goldmuntz, Beverly S Emanuel, Douglas Ryba, James William Gaynor, Elaine H Zackai, Hakon Hakonarson, Donna M McDonald-McGinn
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study. Genes 14 (1) (2022)
Daniel E McGinn, Terrence Blaine Crowley, Tracy Heung, Oanh Tran, Edward Moss, Elaine H Zackai, Beverly S Emanuel, Eva W C Chow, Bernice E Morrow, Ann Swillen, Anne Susan Bassett, Donna M McDonald-McGinn
Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome. Genes 13 (10) (2022)
Hayley A Ron, Terrence Blaine Crowley, Yichuan Liu, Marta Unolt, Erica Schindewolf, Julie Moldenhauer, Jack Rychik, Elizabeth Goldmuntz, Beverly S Emanuel, Douglas Ryba, James William Gaynor, Elaine H Zackai, Hakon Hakonarson, Donna M McDonald-McGinn
Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study. Genes 14 (1) (2022)
Steven Pastor, Oanh Tran, Daniel E McGinn, Terrence Blaine Crowley, Elaine H Zackai, Donna M McDonald-McGinn, Beverly S Emanuel
A Novel Non-Allelic Homologous Recombination Event in a Parent with an 11;22 Reciprocal Translocation Leading to 22q11.2 Deletion Syndrome. Genes 13 (9) (2022)
Ruben E Gur, Tyler M Moore, Ronnie Weinberger, Ehud Mekori-Domachevsky, Raz Gross, Beverly S Emanuel, Elaine H Zackai, Edward Moss, Robert Sean Gallagher, Daniel E McGinn, Terrence Blaine Crowley, Donna McDonald-McGinn, Doron Gothelf, Raquel E Gur
Relationship between intelligence quotient measures and computerized neurocognitive performance in 22q11.2 deletion syndrome. Brain and behavior 11 (8) (2021)
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, Tracy Heung, Aaron M Holleman, H Richard Johnston, Thomas Monfeuga, Donna M McDonald-McGinn, Raquel E Gur, Bernice E Morrow, Ann Swillen, Jacob A S Vorstman, Carrie E Bearden, Eva W C Chow, Marianne van den Bree, Beverly S Emanuel, Joris R Vermeesch, Stephen T Warren, Michael J Owen, Pankaj Chopra, David J Cutler, Richard Duncan, Alex V Kotlar, Jennifer G Mulle, Anna J Voss, Michael E Zwick, Alexander Diacou, Aaron Golden, Tingwei Guo, Jhih-Rong Lin, Tao Wang, Zhengdong Zhang, Yingjie Zhao, Christian R Marshall, Daniele Merico, Andrea Jin, Brenna Lilley, Harold I Salmons, Oanh Tran, Peter Holmans, Antonio F Pardinas, James T R Walters, Wolfram Demaerel, Erik Boot, Nancy J Butcher, Gregory A Costain, Chelsea Lowther, Rens Evers, Therese A M J van Amelsvoort, Esther van Duin, Claudia Vingerhoets, Jeroen Breckpot, Koen Devriendt, Elfi Vergaelen, Annick Vogels, Terrence Blaine Crowley, Daniel E McGinn, Edward M Moss, Robert J Sharkus, Marta Unolt, Elaine H Zackai, Monica E Calkins, Robert S Gallagher, Ruben C Gur, Sunny X Tang, Rosemarie Fritsch, Claudia Ornstein, Gabriela M Repetto, Elemi Breetvelt, Sasja N Duijff, Ania M Fiksinski, Hayley Moss, Maria Niarchou, Kieran C Murphy, Sarah E Prasad, Eileen M Daly, Maria Gudbrandsen, Clodagh M Murphy, Declan G M Murphy, Antonio Buzzanca, Fabio Di Fabio, Maria C Digilio, Maria Pontillo, Bruno Marino, Stefano Vicari, Karlene Coleman, Joseph F Cubells, Opal Y Ousley, Miri Carmel, Doron Gothelf, Ehud Mekori-Domachevsky, Elena Michaelovsky, Ronnie Weinberger, Abraham Weizman, Leila Kushan, Maria Jalbrzikowski, Marco Armando, Stéphan Eliez, Corrado Sandini, Maude Schneider, Frédérique Sloan Béna, Kevin M Antshel, Wanda Fremont, Wendy R Kates, Raoul Belzeaux, Tiffany Busa, Nicole Philip, Linda E Campbell, Kathryn L McCabe, Stephen R Hooper, Kelly Schoch, Vandana Shashi, Tony J Simon, Flora Tassone, Celso Arango, David Fraguas, Sixto García-Miñaúr, Jaume Morey-Canyelles, Jordi Rosell, Damià H Suñer, Jasna Raventos-Simic, null null, Michael P Epstein, Nigel M Williams, Anne S Bassett
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular psychiatry 26 (8) (2020)
Adam Butensky, Chiara Pandolfi de Rinaldis, Shrey Patel, Sharon Edman, Alice Bailey, Daniel E McGinn, Elaine Zackai, Terrence Blaine Crowley, Donna M McDonald-McGinn, Jungwon Min, Elizabeth Goldmuntz
Cardiac evaluation of patients with 22q11.2 duplication syndrome. American journal of medical genetics. Part A 185 (3) (2020)
Jelle F Homans, Terrence Blaine Crowley, Erin Chen, Daniel E McGinn, Vincent F X Deeney, Ralph J B Sakkers, Richard S Davidson, René M Castelein, Donna M McDonald-McGinn
Club foot in association with the 22q11.2 deletion syndrome: An observational study. American journal of medical genetics. Part A 176 (10) (2019)
Ian M Campbell, Sarah E Sheppard, Terrence Blaine Crowley, Daniel E McGinn, Alice Bailey, Michael J McGinn, Marta Unolt, Jelle F Homans, Erin Y Chen, Harold I Salmons, J William Gaynor, Elizabeth Goldmuntz, Oksana A Jackson, Lorraine E Katz, Maria R Mascarenhas, Vincent F X Deeney, René M Castelein, Karen B Zur, Lisa Elden, Staci Kallish, Thomas F Kolon, Sarah E Hopkins, Madeline A Chadehumbe, Michele P Lambert, Brian J Forbes, Julie S Moldenhauer, Erica M Schindewolf, Cynthia B Solot, Edward M Moss, Raquel E Gur, Kathleen E Sullivan, Beverly S Emanuel, Elaine H Zackai, Donna M McDonald-McGinn
What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia. American journal of medical genetics. Part A 176 (10) (2019)
Marta Unolt, Molka Kammoun, Sebastian Kwiatkowski, Gail E Graham, Terrence Blaine Crowley, Matthew S Hestand, Wolfram Demaerel, Maciej Geremek, Beverly S Emanuel, Elaine H Zackai, Joris R Vermeesch, Donna M McDonald-McGinn
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition. Genetics in medicine : official journal of the American College of Medical Genetics 22 (2) (2019)
Oksana Jackson, Terrence Blaine Crowley, Robert Sharkus, Robert Smith, Stephanie Jeong, Cynthia B Solot, Donna McDonald-Mcginn
Palatal evaluation and treatment in 22q11.2 deletion syndrome. American journal of medical genetics. Part A 179 (7) (2019)
Jason P Van Batavia, Terrence Blaine Crowley, Evanette Burrows, Elaine H Zackai, Simone Sanna-Cherchi, Donna M McDonald-McGinn, Thomas F Kolon
Anomalies of the genitourinary tract in children with 22q11.2 deletion syndrome. American journal of medical genetics. Part A 179 (3) (2018)
Jennifer L Cohen, Terrence Blaine Crowley, Daniel E McGinn, Carey McDougall, Marta Unolt, Michele P Lambert, Beverly S Emanuel, Elaine H Zackai, Donna M McDonald-McGinn
22q and two: 22q11.2 deletion syndrome and coexisting conditions. American journal of medical genetics. Part A 176 (10) (2018)
E Verheij, L Elden, Terrence Blaine Crowley, Frank A Pameijer, Elaine H Zackai, Donna M McDonald-McGinn, Henricus G X M Thomeer
Anatomic Malformations of the Middle and Inner Ear in 22q11.2 Deletion Syndrome: Case Series and Literature Review. AJNR. American journal of neuroradiology 39 (5) (2018)

Terrence Blaine Crowley.css-eqlu8i{font-size:small;padding-left:4px;} (Terrence B Crowley, T B Crowley, T Blaine Crowley, T Blaine Crowley)

Publication Activity (10 Years)

Top Topics

Top Venues

Terrence Blaine Crowley (Terrence B Crowley, T B Crowley, T Blaine Crowley, T Blaine Crowley)