How family histories can inform research about germ cell exposures: the example of autism von Escher, Jill

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Pregnancy drugs, fetal germline epigenome, and risks for next‐generation pathology: A call to action von Escher, Jill, Robotti, Suzanne

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Bugs in the program: can pregnancy drugs and smoking disturb molecular reprogramming of the fetal germline, increasing heritable risk for autism and neurodevelopmental disorders? von Escher, Jill

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A full semantic toolbox is essential for autism research and practice to thrive von Singer, Alison, Lutz, Amy, Escher, Jill, Halladay, Alycia

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Exploring the role of nongenetic inheritance in the etiology of human disease von Escher, Jill, Corces, Victor, Mansuy, Isabelle, Yan, Wei

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Exploring the role of nongenetic inheritance in the etiology of human disease von Escher, Jill, Corces, Victor, Mansuy, Isabelle, Yan, Wei

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Response to letter from Ryan Collis von Lutz, Amy, Singer, Alison, Escher, Jill, Halladay, Alycia

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Response to Natri von Singer, Alison, Escher, Jill, Lutz, Amy, Halladay, Alycia

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Beyond Genes: Germline Disruption in the Etiology of Autism Spectrum Disorders von Escher, Jill, Yan, Wei, Rissman, Emilie F., Wang, Hsiao-Lin V., Hernandez, Arturo, Corces, Victor G.

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General anesthesia, germ cells and the missing heritability of autism: an urgent need for research von Escher, Jill, Ford, La Donna

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Heritable hazards of smoking: Applying the “clean sheet” framework to further science and policy von Bline, Abigail P., Dearfield, Kerry L., DeMarini, David M., Marchetti, Francesco, Yauk, Carole L., Escher, Jill

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Induction of ER Stress by an AAV5 BDD FVIII Construct Is Dependent on the Strength of the Hepatic-Specific Promoter von Fong, Sylvia, Handyside, Britta, Sihn, Choong-Ryoul, Liu, Su, Zhang, Lening, Xie, Lin, Murphy, Ryan, Galicia, Nicole, Yates, Bridget, Minto, Wesley C., Vitelli, Catherine, Harmon, Danielle, Ru, Yuanbin, Yu, Guoying Karen, Escher, Claudia, Vowinckel, Jakob, Woloszynek, Jill, Akeefe, Hassib, Mahimkar, Rajeev, Bullens, Sherry, Bunting, Stuart

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SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function von Li, Man, Li, Yong, Weeks, Olivia, Mijatovic, Vladan, Teumer, Alexander, Huffman, Jennifer E, Tromp, Gerard, Fuchsberger, Christian, Gorski, Mathias, Lyytikäinen, Leo-Pekka, Nutile, Teresa, Sedaghat, Sanaz, Sorice, Rossella, Tin, Adrienne, Yang, Qiong, Ahluwalia, Tarunveer S, Arking, Dan E, Bihlmeyer, Nathan A, Böger, Carsten A, Carroll, Robert J, Chasman, Daniel I, Cornelis, Marilyn C, Dehghan, Abbas, Faul, Jessica D, Feitosa, Mary F, Gambaro, Giovanni, Gasparini, Paolo, Giulianini, Franco, Heid, Iris, Huang, Jinyan, Imboden, Medea, Jackson, Anne U, Jeff, Janina, Jhun, Min A, Katz, Ronit, Kifley, Annette, Kilpeläinen, Tuomas O, Kumar, Ashish, Laakso, Markku, Li-Gao, Ruifang, Lohman, Kurt, Lu, Yingchang, Mägi, Reedik, Malerba, Giovanni, Mihailov, Evelin, Mohlke, Karen L, Mook-Kanamori, Dennis O, Robino, Antonietta, Ruderfer, Douglas, Salvi, Erika, Schick, Ursula M, Schulz, Christina-Alexandra, Smith, Albert V, Smith, Jennifer A, Traglia, Michela, Yerges-Armstrong, Laura M, Zhao, Wei, Goodarzi, Mark O, Kraja, Aldi T, Liu, Chunyu, Wessel, Jennifer, Boerwinkle, Eric, Borecki, Ingrid B, Bork-Jensen, Jette, Bottinger, Erwin P, Braga, Daniele, Brandslund, Ivan, Brody, Jennifer A, Campbell, Archie, Carey, David J, Christensen, Cramer, Coresh, Josef, Crook, Errol, Curhan, Gary C, Cusi, Daniele, de Boer, Ian H, de Vries, Aiko P J, Denny, Joshua C, Devuyst, Olivier, Dreisbach, Albert W, Endlich, Karlhans, Esko, Tõnu, Franco, Oscar H, Fulop, Tibor, Gerhard, Glenn S, Glümer, Charlotte, Gottesman, Omri, Grarup, Niels, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B, Hayward, Caroline, Hocking, Lynne, Hofman, Albert, Hu, Frank B, Husemoen, Lise Lotte N, Jackson, Rebecca D, Jørgensen, Torben, Jørgensen, Marit E, Kähönen, Mika

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Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility von Hidalgo, Bertha, An, Ping, Lu, Yingchang, Rasmussen-Torvik, Laura J, Grarup, Niels, Ehm, Margaret G, Stančáková, Alena, Boland, Anne, Freitag, Daniel F, Garcia, Melissa E, Guo, Xiuqing, Isaacs, Aaron, Jakobsdottir, Johanna, Lange, Leslie A, Hua Zhao, Jing, Meidtner, Karina, Morrison, Alanna C, Peters, Marjolein J, Smith, Albert V, Varga, Tibor V, Allin, Kristine H, Aung, Tin, Barbieri, Caterina, Burns, Sean M, Chen, Yuning, Chen, Yii-DerI, Czajkowski, Jacek, Dehghan, Abbas, Eiriksdottir, Gudny, Escher, Stefan A, Goddard, William A, Gottesman, Omri, Gustafsson, Stefan, Hai, Yang, Ikram, Mohammad K, Jørgensen, Marit E, Jørgensen, Torben, Karaleftheri, Maria, Khor, Chiea C, Kuusisto, Johanna, Lange, Ethan M, Lee, Wen-Jane, Liu, Chunyu, Liu, Yongmei, McLeod, Olga, Ntalla, Ioanna, Palmer, Nicholette D, Rayner, Nigel W, Rice, Ken, Sennblad, Bengt, Serafetinidis, Ioannis, Smith, Jennifer A, Soranzo, Nicole, Stahl, Eli A, Torres, Mina, Yanek, Lisa R, Zengini, Eleni, Bis, Joshua C, Adrienne Cupples, L, Hansen, Torben, Ingelsson, Erik, Lorenzo, Carlos, Mathias, Rasika A, Norris, Jill M, Peloso, Gina M, Sheu, Wayne H.-H, Vaidya, Dhananjay, Wagenknecht, Lynne E, Bottinger, Erwin P, Ferrannini, Ele, Franks, Paul W, Gibbs, Richard A, Launer, Lenore J, Polasek, Ozren, Province, Michael A, Walker, Mark, Wong, Tien Y, Forouhi, Nita G, Lucarelli, Debora ME, Sims, Matt, McCarthy, Mark I, Barricarte, Aurelio, Gonzalez, Carlos, Kaaks, Rudolf, Key, Timothy J, Navarro, Carmen, Nilsson, Peter M, Overvad, Kim, Panico, Salvatore, Quirós, J. Ramón, van der Schouw, Yvonne T, Psaty, Bruce M, Shyong Tai, E, van Duijn, Cornelia M, Florez, Jose C, Loos, Ruth J.F, Wilson, James G, Frayling, Timothy M, Rotter, Jerome I, Goodarzi, Mark O

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Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility von Wang, Shuai, Dauriz, Marco, Hivert, Marie-France, Hidalgo, Bertha, An, Ping, Lu, Yingchang, Rasmussen-Torvik, Laura J, Grarup, Niels, Ehm, Margaret G, Baldridge, Abigail S, Stančáková, Alena, Boland, Anne, Freitag, Daniel F, Garcia, Melissa E, Guo, Xiuqing, Isaacs, Aaron, Jakobsdottir, Johanna, Lange, Leslie A, Hua Zhao, Jing, Meidtner, Karina, Morrison, Alanna C, Peters, Marjolein J, Smith, Albert V, Varga, Tibor V, Allin, Kristine H, Aung, Tin, Barbieri, Caterina, Bombieri, Cristina, Burns, Sean M, Chen, Yuning, Chen, Yii-DerI, Czajkowski, Jacek, Dehghan, Abbas, Eiriksdottir, Gudny, Escher, Stefan A, Farmaki, Aliki-Eleni, Frånberg, Mattias, Giulianini, Franco, Goddard, William A, Gottesman, Omri, Gustafsson, Stefan, Hai, Yang, Hoffmann, Per, Ikram, Mohammad K, Jensen, Richard A, Jørgensen, Marit E, Jørgensen, Torben, Karaleftheri, Maria, Khor, Chiea C, Kuusisto, Johanna, Lange, Ethan M, Lee, IT, Lee, Wen-Jane, Liu, Chunyu, Liu, Yongmei, McLeod, Olga, Ntalla, Ioanna, Palmer, Nicholette D, Pasko, Dorota, Rayner, Nigel W, Rice, Ken, Sennblad, Bengt, Serafetinidis, Ioannis, Smith, Jennifer A, Soranzo, Nicole, Speliotes, Elizabeth K, Stahl, Eli A, Torres, Mina, Javad, Sundas, Yanek, Lisa R, Zengini, Eleni, Bis, Joshua C, Hansen, Torben, Ingelsson, Erik, Lorenzo, Carlos, Mathias, Rasika A, Norris, Jill M, Peloso, Gina M, Toniolo, Daniela, Vaidya, Dhananjay, Wagenknecht, Lynne E, Bottinger, Erwin P, Ferrannini, Ele, Franks, Paul W, Gibbs, Richard A, Launer, Lenore J, Padmanabhan, Sandosh, Polasek, Ozren, Province, Michael A, Ridker, Paul M, Walker, Mark, Wong, Tien Y, Tai, E Shyong, Kao, WH Linda, Florez, Jose C, Loos, Ruth JF, Wilson, James G, Siscovick, David S, Meigs, James B, Scott, Robert A

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