Evidence for Maternal-Fetal Genotype Incompatibility as a Risk Factor for Schizophrenia

por Palmer, Christina G. S.
Publicado 2010

Examining the Relationship Between Genetic Counselors’ Attitudes Toward Deaf People and the Genetic Counseling Session

por Enns, Emily E., Boudreault, Patrick, Palmer, Christina G. S.
Publicado 2010

Impact of Genetic Counseling and Connexin-26 and Connexin-30 Testing on Deaf Identity and Comprehension of Genetic Test Results in a Sample of Deaf Adults: A Prospective, Longitudi...

por Palmer, Christina G. S., Boudreault, Patrick, Baldwin, Erin E., Sinsheimer, Janet S.
Publicado 2014

Using a social marketing framework to evaluate recruitment of a prospective study of genetic counseling and testing for the deaf community

por Kobayashi, Yoko, Boudreault, Patrick, Hill, Karin, Sinsheimer, Janet S, Palmer, Christina GS
Publicado 2013

Effect of Pre-test Genetic Counseling for Deaf Adults on Knowledge of Genetic Testing

por Baldwin, Erin E., Boudreault, Patrick, Fox, Michelle, Sinsheimer, Janet S., Palmer, Christina G. S.
Publicado 2012

Publishing a Master’s Thesis: A Guide for Novice Authors

por Resta, Robert G., McCarthy Veach, Patricia, Charles, Sarah, Vogel, Kristen, Blase, Terri, Palmer, Christina G. S.
Publicado 2010

Using the maternal-fetal genotype incompatibility test to assess non-inherited maternal HLA-DRB1 antigen coding alleles as rheumatoid arthritis risk factors

por Hsieh, Hsin-Ju, Palmer, Christina GS, Harney, Sinead, Chen, Hsiu-Wen, Bauman, Lara, Brown, Matthew A, Sinsheimer, Janet S
Publicado 2007

Virtual Care for Behavioral Health Conditions

por Palmer, Christina S., Brown Levey, Shandra M., Kostiuk, Marisa, Zisner, Aimee R., Tolle, Lauren Woodward, Richey, Rebecca M., Callan, Stephanie
Publicado 2022

Effect of Rhesus D incompatibility on schizophrenia depends on offspring sex

por Palmer, Christina G.S., Mallery, Erin, Turunen, Joni A., Hsieh, Hsin-Ju, Peltonen, Leena, Lonnqvist, Jouko, Woodward, J. Arthur, Sinsheimer, Janet S.
Publicado 2008

Physical activity and telomere length in early stage breast cancer survivors

por Garland, Sheila N, Johnson, Brad, Palmer, Christina, Speck, Rebecca M, Donelson, Michelle, Xie, Sharon X, DeMichele, Angela, Mao, Jun J
Publicado 2014

The role of a sequencing-based clinical intestinal screening test in patients at high-risk for Clostridium difficile and other pathogens: a case report

por Hitschfeld, Maureen, Tovar, Elena, Gupta, Sarah, Bik, Elisabeth M., Palmer, Christina, Hoaglin, Michael C., Almonacid, Daniel E., Richman, Jessica, Apte, Zachary S.
Publicado 2019

Myopathy associated with homozygous PYROXD1 pathogenic variants detected by genome sequencing

por Woods, Jeremy D., Khanlou, Negar, Lee, Hane, Signer, Rebecca, Shieh, Perry, Chen, Johnathan, Herzog, Matthew, Palmer, Christina, Martinez‐Agosto, Julian, Nelson, Stanley F.
Publicado 2020

Asymptomatic deer excrete infectious prions in feces

por Tamgüney, Gültekin, Miller, Michael W., Wolfe, Lisa L., Sirochman, Tracey M., Glidden, David V., Palmer, Christina, Lemus, Azucena, DeArmond, Stephen J., Prusiner, Stanley B.
Publicado 2009

Gut microbiome composition and risk factors in a large cross-sectional IBS cohort

por Agnello, Melissa, Carroll, Lauren N, Imam, Nabeel, Pino, Rodolfo, Palmer, Christina, Varas, Ignacio, Greene, Claire, Hitschfeld, Maureen, Gupta, Sarah, Almonacid, Daniel E, Hoaglin, Michael C
Publicado 2020

Protease-Sensitive Synthetic Prions

por Colby, David W., Wain, Rachel, Baskakov, Ilia V., Legname, Giuseppe, Palmer, Christina G., Nguyen, Hoang-Oanh B., Lemus, Azucena, Cohen, Fred E., DeArmond, Stephen J., Prusiner, Stanley B.
Publicado 2010

Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network

por Palmer, Christina G. S., McConkie-Rosell, Allyn, Holm, Ingrid A., LeBlanc, Kimberly, Sinsheimer, Janet S., Briere, Lauren C., Dorrani, Naghmeh, Herzog, Matthew R., Lincoln, Sharyn, Schoch, Kelly, Spillmann, Rebecca C., Brokamp, Elly
Publicado 2018

Self-Sampling for Human Papillomavirus Testing: Increased Cervical Cancer Screening Participation and Incorporation in International Screening Programs

por Gupta, Sarah, Palmer, Christina, Bik, Elisabeth M., Cardenas, Juan P., Nuñez, Harold, Kraal, Laurens, Bird, Sara W., Bowers, Jennie, Smith, Alison, Walton, Nathaniel A., Goddard, Audrey D., Almonacid, Daniel E., Zneimer, Susan, Richman, Jessica, Apte, Zachary S.
Publicado 2018

Novel NUDT2 variant causes intellectual disability and polyneuropathy

por Diaz, Frank, Khosa, Shaweta, Niyazov, Dmitriy, Lee, Hane, Person, Richard, Morrow, Michelle M., Signer, Rebecca, Dorrani, Naghmeh, Zheng, Allison, Herzog, Matthew, Freundlich, Robert, Birath, J. Brandon, Cervantes‐Manzo, Yurivia, Martinez‐Agosto, Julian A., Palmer, Christina, Nelson, Stanley F., Fogel, Brent L., Mishra, Shri K.
Publicado 2020

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

por Marbach, Felix, Stoyanov, Georgi, Erger, Florian, Stratakis, Constantine A., Settas, Nikolaos, London, Edra, Rosenfeld, Jill A., Torti, Erin, Haldeman-Englert, Chad, Sklirou, Evgenia, Kessler, Elena, Ceulemans, Sophia, Nelson, Stanley F., Martinez-Agosto, Julian A., Palmer, Christina G. S., Signer, Rebecca H., Andrews, Marisa V., Grange, Dorothy K., Willaert, Rebecca, Person, Richard, Telegrafi, Aida, Sievers, Aaron, Laugsch, Magdalena, Theiß, Susanne, Cheng, YuZhu, Lichtarge, Olivier, Katsonis, Panagiotis, Stocco, Amber, Schaaf, Christian P.
Publicado 2021

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

por Bryant, Laura, Li, Dong, Cox, Samuel G., Marchione, Dylan, Joiner, Evan F., Wilson, Khadija, Janssen, Kevin, Lee, Pearl, March, Michael E., Nair, Divya, Sherr, Elliott, Fregeau, Brieana, Wierenga, Klaas J., Wadley, Alexandrea, Mancini, Grazia M. S., Powell-Hamilton, Nina, van de Kamp, Jiddeke, Grebe, Theresa, Dean, John, Ross, Alison, Crawford, Heather P., Powis, Zoe, Cho, Megan T., Willing, Marcia C., Manwaring, Linda, Schot, Rachel, Nava, Caroline, Afenjar, Alexandra, Lessel, Davor, Wagner, Matias, Klopstock, Thomas, Winkelmann, Juliane, Catarino, Claudia B., Retterer, Kyle, Schuette, Jane L., Innis, Jeffrey W., Pizzino, Amy, Lüttgen, Sabine, Denecke, Jonas, Strom, Tim M., Monaghan, Kristin G., Yuan, Zuo-Fei, Dubbs, Holly, Bend, Renee, Lee, Jennifer A., Lyons, Michael J., Hoefele, Julia, Günthner, Roman, Reutter, Heiko, Keren, Boris, Radtke, Kelly, Sherbini, Omar, Mrokse, Cameron, Helbig, Katherine L., Odent, Sylvie, Cogne, Benjamin, Mercier, Sandra, Bezieau, Stephane, Besnard, Thomas, Kury, Sebastien, Redon, Richard, Reinson, Karit, Wojcik, Monica H., Õunap, Katrin, Ilves, Pilvi, Innes, A. Micheil, Kernohan, Kristin D., Costain, Gregory, Meyn, M. Stephen, Chitayat, David, Zackai, Elaine, Lehman, Anna, Kitson, Hilary, Martin, Martin G., Martinez-Agosto, Julian A., Nelson, Stan F., Palmer, Christina G. S., Papp, Jeanette C., Parker, Neil H., Sinsheimer, Janet S., Vilain, Eric, Wan, Jijun, Yoon, Amanda J., Zheng, Allison, Brimble, Elise, Ferrero, Giovanni Battista, Radio, Francesca Clementina, Carli, Diana, Barresi, Sabina, Brusco, Alfredo, Tartaglia, Marco, Thomas, Jennifer Muncy, Umana, Luis, Weiss, Marjan M., Gotway, Garrett, Stuurman, K. E., Thompson, Michelle L., McWalter, Kirsty, Stumpel, Constance T. R. M., Stevens, Servi J. C., Stegmann, Alexander P. A., Tveten, Kristian, Vøllo, Arve, Prescott, Trine, Fagerberg, Christina, Laulund, Lone Walentin, Larsen, Martin J., Byler, Melissa, Lebel, Robert Roger, Hurst, Anna C., Dean, Joy, Schrier Vergano, Samantha A., Norman, Jennifer, Mercimek-Andrews, Saadet, Neira, Juanita, Van Allen, Margot I., Longo, Nicola, Sellars, Elizabeth, Louie, Raymond J., Cathey, Sara S., Brokamp, Elly, Heron, Delphine, Snyder, Molly, Vanderver, Adeline, Simon, Celeste, de la Cruz, Xavier, Padilla, Natália, Crump, J. Gage, Chung, Wendy, Garcia, Benjamin, Hakonarson, Hakon H., Bhoj, Elizabeth J.
Publicado 2020