Design of “Low Stress” Post-CMP Cleaning Processes for Advanced Technology Nodes by Cahue, Kiana A., Dudek, Abigail L., Miliauskas, Mantas M., Cahue, Tatiana R., Mlynarski, Amy, Keleher, Jason J.

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Synergistic Effect of Pad "Macroporous-Reactors" on Passivation Mechanisms to Modulate Cu Chemical Mechanical Planarization (CMP) Performance by Wortman-Otto, Katherine M., Graverson, Carolyn F., Linhart, Abigail N., McDonough, Rose K., Mlynarski, Amy L., Keleher, Jason J.

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Copy Number Variation of the glucose transporter gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome by Mlynarski, Elisabeth E., Sheridan, Molly B., Xie, Michael, Guo, Tingwei, Racedo, Silvia E., McDonald McGinn, Donna M., Gai, Xiaowu, Chow, Eva W.C., Vorstman, Jacob, Swillen, Ann, Devriendt, Koen, Breckpot, Jeroen, Digilio, Maria Cristina, Marino, Bruno, Dallapiccola, Bruno, Philip, Nicole, Simon, Tony J., Roberts, Amy E., Piotrowicz, Małgorzata, Bearden, Carrie E., Eliez, Stephan, Gothelf, Doron, Coleman, Karlene, Kates, Wendy R., Devoto, Marcella, Zackai, Elaine, Heine-Suñer, Damian, Shaikh, Tamim H., Bassett, Anne S., Goldmuntz, Elizabeth, Morrow, Bernice E., Emanuel, Beverly S.

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Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome by Mlynarski, Elisabeth E., Xie, Michael, Taylor, Deanne, Sheridan, Molly B., Guo, Tingwei, Racedo, Silvia E., McDonald-McGinn, Donna M., Chow, Eva W. C., Vorstman, Jacob, Swillen, Ann, Devriendt, Koen, Breckpot, Jeroen, Digilio, Maria Cristina, Marino, Bruno, Dallapiccola, Bruno, Philip, Nicole, Simon, Tony J., Roberts, Amy E., Piotrowicz, Małgorzata, Bearden, Carrie E., Eliez, Stephan, Gothelf, Doron, Coleman, Karlene, Kates, Wendy R., Devoto, Marcella, Zackai, Elaine, Heine- Suñer, Damian, Goldmuntz, Elizabeth, Bassett, Anne S., Morrow, Bernice E., Emanuel, Beverly S.

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Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability by Raimondo, Anne, Chakera, Ali J, Thomsen, Soren K, Colclough, Kevin, Barrett, Amy, De Franco, Elisa, Chatelas, Alisson, Demirbilek, Huseyin, Akcay, Teoman, Alawneh, Hussein, Flanagan, Sarah E, Van De Bunt, Martijn, Hattersley, Andrew T, Gloyn, Anna L, Ellard, Sian

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EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome by Farmer, Amy, Aymé, Ségolène, de Heredia, Miguel Lopez, Maffei, Pietro, McCafferty, Susan, Młynarski, Wojciech, Nunes, Virginia, Parkinson, Kay, Paquis-Flucklinger, Véronique, Rohayem, Julia, Sinnott, Richard, Tillmann, Vallo, Tranebjaerg, Lisbeth, Barrett, Timothy G

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Role of 657del5 NBN mutation and 7p12.2 ( IKZF1 ), 9p21 ( CDKN2A ), 10q21.2 ( ARID5B ) and 14q11.2 ( CEBPE ) variation and risk of childhood ALL in the Polish population by Pastorczak, Agata, Górniak, Patryk, Sherborne, Amy, Hosking, Fay, Trelińska, Joanna, Lejman, Monika, Szczepański, Tomasz, Borowiec, Maciej, Fendler, Wojciech, Kowalczyk, Jerzy, Houlston, Richard S, Młynarski, Wojciech

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http://www.euro-wabb.org: an EU Register for Alstrom, Bardet Biedl and other rare syndromes by Barrett, T, Farmer, A, Aymé, S, Maffei, P, McCafferty, S, Mlynarski, W, Nunes, V, Paquis, V, Parkinson, K, Rohayem, J, Sinnott, R, Tillmann, V, Tranebjaerg, L

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Turning over the Beds – How Optimizing Pre-Discharge Patient Teaching Reduced Discharge Delays in the Inpatient Hospital at Dana-Farber Cancer Institute and Brigham and Women's Hos... by Solle, Justin Cook, Close, Sara, Koch, Brandon, Hartley, Tricia, Steinberg, Alexis, Pullo, Anna, Guerrero, Caitlin, Mlynarski, Daria, Daniels, Lauren, Curran, Shauna, Gould, Katie, Glotzbecker, Brett, Emmert, Amy B.

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