Identification of novel coding mutation in C1qA gene in an African–American pedigree with lupus and C1q deficiency by Namjou, B, Keddache, M, Fletcher, D, Dillon, S, Kottyan, L, Wiley, G, Gaffney, PM, Wakeland, BE, Liang, C, Wakeland, EK, Scofield, RH, Kaufman, K, Harley, JB

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Impact of Population Stratification on Family-Based Association in an Admixed Population by Fardo, David W., Martin, L. J., Pilipenko, V., Kurowski, B. G., Zhang, X., Alexander, E. S., He, H., Ding, Lili, Mersha, T. B., Kottyan, L.

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Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations by Kim-Howard, Xana, Sun, Celi, Molineros, Julio E, Maiti, Amit K, Chandru, Hema, Adler, Adam, Wiley, Graham B, Kaufman, Kenneth M, Kottyan, Leah, Guthridge, Joel M, Rasmussen, Astrid, Kelly, Jennifer, Sánchez, Elena, Raj, Prithvi, Li, Quan-Zhen, Bang, So-Young, Lee, Hye-Soon, Kim, Tae-Hwan, Kang, Young Mo, Suh, Chang-Hee, Chung, Won Tae, Park, Yong-Beom, Choe, Jung-Yoon, Shim, Seung Cheol, Lee, Shin-Seok, Han, Bok-Ghee, Olsen, Nancy J, Karp, David R, Moser, Kathy, Pons-Estel, Bernardo A, Wakeland, Edward K, James, Judith A, Harley, John B, Bae, Sang-Cheol, Gaffney, Patrick M, Alarcón-Riquelme, Marta, Looger, Loren L, Nath, Swapan K

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X Chromosome Dose and Sex Bias in Autoimmune Diseases by Liu, Ke, Kurien, Biji T., Zimmerman, Sarah L., Kaufman, Kenneth M., Taft, Diana H., Kottyan, Leah C., Lazaro, Sara, Weaver, Carrie A., Ice, John A., Adler, Adam J., Chodosh, James, Radfar, Lida, Rasmussen, Astrid, Stone, Donald U., Lewis, David M., Li, Shibo, Koelsch, Kristi A., Igoe, Ann, Talsania, Mitali, Kumar, Jay, Maier-Moore, Jacen S., Harris, Valerie M., Gopalakrishnan, Rajaram, Jonsson, Roland, Lessard, James A., Lu, Xianglan, -Eric Gottenberg, Jacques, -Manuel Anaya, Juan, Cunninghame-Graham, Deborah S., Huang, Andrew J. W., Brennan, Michael T., Hughes, Pamela, Mei, Gabor G., Miceli-Richard, Corinne, Keystone, Edward C., Bykerk, Vivian P., Hirschfield, Gideon, Xie, Gang, Ng, Wan-Fai, Nordmark, Gunnel, Eriksson, Per, Omda, Roald, Rhodus, Nelson L., Rischmueller, Maureen, Rohrer, Michael, Sega, Barbara M., Vvse, Timothy J., Wahren-Herlenius, Marie, Witte, Torsten, Pons-Este, Bernardo, Alarcon-Riquelme, Marta E., Guthridge, Joel M., James, Judith A., Lessard, Christopher J., Kelly, Jennifer A., Thompson, Susan D., Gaffney, Patrick M., Montgomery, Courtney G., Edberg, Jeffrey C., Kimberly, Robert P., Alarcon, Gracicla S., Langefeld, Carl L., Gilkeson, Gary S., Kamen, Diane L., Tsao, Betty P., Joseph McCune, W., Salmon, Jane E., Merrill, Joan T., Weisman, Michael H., Wallace, Daniel J., Utset, Tammy, Bottinger, Erwin P., Amos, Christopher I., Siminovitch, Katherine A., Mariette, Xavier, Sivils, Kathy L., Harley, John B., Hal Scofield, R.

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X chromosome dose and sex bias in autoimmune diseases: increased 47,XXX in systemic lupus erythematosus and Sjögren’s syndrome (BA4P.211) by Liu, Ke, Kurien, Biji, Zimmerman, Sarah, Kaufman, Kenneth, Mariette, Xavier, Kottyan, Leah, Jonsson, Roland, Ng, Wan-Fai, Omdal, Roald, Rischmueller, Maureen, Wahren-herlenius, Marie, James, Judith, Lessard, Christopher, Thompson, Susan, Gaffney, Patrick, Montgomery, Courtney, Siminovitch, Katherine, Edberg, Jeffrey, Kimberly, Robert, Tsao, Betty, McCune, W., Salmon, Jane, Sivils, Kathy, Harley, John, Scofield, R.

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Eosinophils Respond to Acidic Environments with cAMP Production, Decreased Apoptosis, and a Decrease in the Expression of Pro-apoptotic Bcl-2 Family Members by Kottyan, L.C, Hedgebeth, M.H, Niese, K.A, Cao, K.H, Hildeman, D.A, Montrose, M.H, Rothenberg, M.E, Zimmermann, N

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Eosinophils Respond to Acidic environments with cAMP Generation in a TDAG8-Dependent Manner by Kottyan, L.C, Collier, A.R, Niese, K.A, Radu, C.O, Witte, O.N, Rothenberg, M.E, Zimmermann, N

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Imputation and quality control steps for combining multiple genome-wide datasets by Verma, Shefali S, de Andrade, Mariza, Tromp, Gerard, Kuivaniemi, Helena, Pugh, Elizabeth, Namjou-Khales, Bahram, Mukherjee, Shubhabrata, Jarvik, Gail P, Kottyan, Leah C, Burt, Amber, Bradford, Yuki, Armstrong, Gretta D, Derr, Kimberly, Crawford, Dana C, Haines, Jonathan L, Li, Rongling, Crosslin, David, Ritchie, Marylyn D

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Very early onset eosinophilic esophagitis is common, responds to standard therapy, and demonstrates enrichment for CAPN14 genetic variants by Lyles, John L., Martin, Lisa J., Shoda, Tetsuo, Collins, Margaret H., Trimarchi, Michael P., He, Hua, Kottyan, Leah C., Mukkada, Vincent A., Rothenberg, Marc E.

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Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure by Levin, Michael G., Tsao, Noah L., Singhal, Pankhuri, Liu, Chang, Vy, Ha My T., Paranjpe, Ishan, Backman, Joshua D., Bellomo, Tiffany R., Bone, William P., Biddinger, Kiran J., Hui, Qin, Dikilitas, Ozan, Satterfield, Benjamin A., Yang, Yifan, Morley, Michael P., Bradford, Yuki, Burke, Megan, Reza, Nosheen, Charest, Brian, Judy, Renae L., Puckelwartz, Megan J., Hakonarson, Hakon, Khan, Atlas, Kottyan, Leah C., Kullo, Iftikhar, Luo, Yuan, McNally, Elizabeth M., Rasmussen-Torvik, Laura J., Day, Sharlene M., Do, Ron, Phillips, Lawrence S., Ellinor, Patrick T., Nadkarni, Girish N., Ritchie, Marylyn D., Arany, Zoltan, Cappola, Thomas P., Margulies, Kenneth B., Aragam, Krishna G., Haggerty, Christopher M., Joseph, Jacob, Sun, Yan V., Voight, Benjamin F., Damrauer, Scott M.

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Whole blood transcriptomics identifies gene expression associated with peanut allergy in infants at high risk by Devonshire, Ashley L., Fan, Hanli, Pujato, Mario, Paranjpe, Aditi, Gursel, Demirkan, Schipma, Matthew, Dunn, Julia M., Andorf, Sandra, Pongracic, Jacqueline A., Kottyan, Leah C., Kumar, Rajesh

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Breakthroughs in understanding and treating eosinophilic gastrointestinal diseases presented at the CEGIR/TIGERs Symposium at the 2022 American Academy of Allergy, Asthma & Immunol... by Chehade, Mirna, Wright, Benjamin L, Atkins, Dan, Aceves, Seema S, Ackerman, Steven J, Assa'ad, Amal H, Bauer, Maureen, Collins, Margaret H, Commins, Scott P, Davis, Carla M, Dellon, Evan S, Doerfler, Bethan, Gleich, Gerald J, Gupta, Sandeep K, Hill, David A, Jensen, Elizabeth T, Katzka, David, Kliewer, Kara, Kodroff, Ellyn, Kottyan, Leah C, Kyle, Shay, Muir, Amanda B, Pesek, Robert D, Peterson, Kathryn, Shreffler, Wayne G, Spergel, Jonathan M, Strobel, Mary Jo, Wechsler, Joshua, Zimmermann, Nives, Furuta, Glenn T, Rothenberg, Marc E

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Genome-wide epigenetic profiling and transcriptome analysis in pediatric Obstructive Sleep Apnea: A focus on Black female children by Koritala, Bala S.C., Parameswaran, Sreeja, Donmez, Omer A., Forney, Carmy, Rowden, Hope, Moore, Charles A., Duggins, Angela L., Sestito, Alexandra, Leader, Brittany A., Weirauch, Matthew T., Kottyan, Leah C., Smith, David F.

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Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis by Eapen, Amy A, Parameswaran, Sreeja, Forney, Carmy, Edsall, Lee E, Miller, Daniel, Donmez, Omer, Dunn, Katelyn, Lu, Xiaoming, Granitto, Marissa, Rowden, Hope, Magier, Adam Z, Pujato, Mario, Chen, Xiaoting, Kaufman, Kenneth, Bernstein, David I, Devonshire, Ashley L, Rothenberg, Marc E, Weirauch, Matthew T, Kottyan, Leah C

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CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants by Bray, David, Hook, Heather, Zhao, Rose, Keenan, Jessica L., Penvose, Ashley, Osayame, Yemi, Mohaghegh, Nima, Chen, Xiaoting, Parameswaran, Sreeja, Kottyan, Leah C., Weirauch, Matthew T., Siggers, Trevor

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Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis by Namjou, Bahram, Marsolo, Keith, Caroll, Robert J, Denny, Joshua C, Ritchie, Marylyn D, Verma, Shefali S, Lingren, Todd, Porollo, Aleksey, Cobb, Beth L, Perry, Cassandra, Kottyan, Leah C, Rothenberg, Marc E, Thompson, Susan D, Holm, Ingrid A, Kohane, Isaac S, Harley, John B

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Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits by Liu, Lili, Khan, Atlas, Sanchez-Rodriguez, Elena, Zanoni, Francesca, Li, Yifu, Steers, Nicholas, Balderes, Olivia, Zhang, Junying, Krithivasan, Priya, LeDesma, Robert A., Fischman, Clara, Hebbring, Scott J., Harley, John B., Moncrieffe, Halima, Kottyan, Leah C., Namjou-Khales, Bahram, Walunas, Theresa L., Knevel, Rachel, Raychaudhuri, Soumya, Karlson, Elizabeth W., Denny, Joshua C., Stanaway, Ian B., Crosslin, David, Rauen, Thomas, Floege, Jürgen, Eitner, Frank, Moldoveanu, Zina, Reily, Colin, Knoppova, Barbora, Hall, Stacy, Sheff, Justin T., Julian, Bruce A., Wyatt, Robert J., Suzuki, Hitoshi, Xie, Jingyuan, Chen, Nan, Zhou, Xujie, Zhang, Hong, Hammarström, Lennart, Viktorin, Alexander, Magnusson, Patrik K. E., Shang, Ning, Hripcsak, George, Weng, Chunhua, Rundek, Tatjana, Elkind, Mitchell S. V., Oelsner, Elizabeth C., Barr, R. Graham, Ionita-Laza, Iuliana, Novak, Jan, Gharavi, Ali G., Kiryluk, Krzysztof

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Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration by Liu, Xueping, Helenius, Dorte, Skotte, Line, Beaumont, Robin N., Wielscher, Matthias, Geller, Frank, Juodakis, Julius, Mahajan, Anubha, Bradfield, Jonathan P., Lin, Frederick T. J., Vogelezang, Suzanne, Bustamante, Mariona, Ahluwalia, Tarunveer S., Pitkänen, Niina, Wang, Carol A., Bacelis, Jonas, Borges, Maria C., Zhang, Ge, Bedell, Bruce A., Rossi, Robert M., Skogstrand, Kristin, Peng, Shouneng, Thompson, Wesley K., Appadurai, Vivek, Lawlor, Debbie A., Kalliala, Ilkka, Power, Christine, McCarthy, Mark I., Boyd, Heather A., Marazita, Mary L., Hakonarson, Hakon, Hayes, M. Geoffrey, Scholtens, Denise M., Rivadeneira, Fernando, Jaddoe, Vincent W. V., Vinding, Rebecca K., Bisgaard, Hans, Knight, Bridget A., Pahkala, Katja, Raitakari, Olli, Helgeland, Øyvind, Johansson, Stefan, Njølstad, Pål R., Fadista, João, Schork, Andrew J., Nudel, Ron, Miller, Daniel E., Chen, Xiaoting, Weirauch, Matthew T., Mortensen, Preben Bo, Børglum, Anders D., Nordentoft, Merete, Mors, Ole, Hao, Ke, Ryckman, Kelli K., Hougaard, David M., Kottyan, Leah C., Pennell, Craig E., Lyytikainen, Leo-Pekka, Bønnelykke, Klaus, Vrijheid, Martine, Felix, Janine F., Lowe, William L., Grant, Struan F. A., Hyppönen, Elina, Jacobsson, Bo, Jarvelin, Marjo-Riitta, Muglia, Louis J., Murray, Jeffrey C., Freathy, Rachel M., Werge, Thomas M., Melbye, Mads, Buil, Alfonso, Feenstra, Bjarke

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Multiancestral polygenic risk score for pediatric asthma by Namjou, Bahram, Lape, Michael, Malolepsza, Edyta, DeVore, Stanley B., Weirauch, Matthew T., Dikilitas, Ozan, Jarvik, Gail P., Kiryluk, Krzysztof, Kullo, Iftikhar J., Liu, Cong, Luo, Yuan, Satterfield, Benjamin A., Smoller, Jordan W., Walunas, Theresa L., Connolly, John, Sleiman, Patrick, Mersha, Tesfaye B., Mentch, Frank D., Hakonarson, Hakon, Prows, Cynthia A., Biagini, Jocelyn M., Khurana Hershey, Gurjit K., Martin, Lisa J., Kottyan, Leah

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A Novel Class of Anticancer Compounds Targets the Actin Cytoskeleton in Tumor Cells by STEHN, Justine R, HAASS, Nikolas K, FATH, Thomas, HILL, Timothy A, McCLUSKEY, Adam, SCHEVZOV, Galina, PALMER, Stephen J, HARDEMAN, Edna C, WINLAW, David, REEVE, Vivienne E, DIXON, Ian, WENINGER, Wolfgang, BONELLO MELISSA DESOUZA, Teresa, CRIPE, Timothy P, GUNNING, Peter W, KOTTYAN, Gregg, TREUTLEIN, Herbert, JUN ZENG, NASCIMENTO, Paula R. B. B, SEQUEIRA, Vanessa B, BUTLER, Tanya L, ALLANSON, Munif

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