Large, but Dispersal‐Limited Populations of the Marsh Fritillary Euphydryas aurinia Persist on Abandoned Military Training Areas Three Decades After the End of the Cold War von Schröer, Cindy, Singer, David, Kamp, Johannes

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Mosaic landscapes provide conservation pockets for an endangered species: Colias myrmidone in Romania von Loos, Jacqueline, Schröer, Cindy, Becker, Thomas, Kastal, Agnes, Kortmann, Elena, Dolek, Matthias

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Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders von Boccuto, Luigi, Lauri, Maria, Sarasua, Sara M, Skinner, Cindy D, Buccella, Daniela, Dwivedi, Alka, Orteschi, Daniela, Collins, Julianne S, Zollino, Marcella, Visconti, Paola, Dupont, Barb, Tiziano, Danilo, Schroer, Richard J, Neri, Giovanni, Stevenson, Roger E, Gurrieri, Fiorella, Schwartz, Charles E

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A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures von Eichler, Evan E, Sharp, Andrew J, Mefford, Heather C, Li, Kelly, Baker, Carl, Skinner, Cindy, Stevenson, Roger E, Schroer, Richard J, Novara, Francesca, De Gregori, Manuela, Ciccone, Roberto, Broomer, Adam, Casuga, Iris, Wang, Yu, Xiao, Chunlin, Barbacioru, Catalin, Gimelli, Giorgio, Bernardina, Bernardo Dalla, Torniero, Claudia, Giorda, Roberto, Regan, Regina, Murday, Victoria, Mansour, Sahar, Fichera, Marco, Castiglia, Lucia, Failla, Pinella, Ventura, Mario, Jiang, Zhaoshi, Cooper, Gregory M, Knight, Samantha J L, Romano, Corrado, Zuffardi, Orsetta, Chen, Caifu, Schwartz, Charles E

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Autistic Disorder: A 20 Year Chronicle von Skinner, Cindy, Pauly, Rini, Skinner, Steven A., Schroer, Richard J., Simensen, Richard J., Taylor, Harold A., Friez, Michael J., DuPont, Barbara R., Stevenson, Roger E.

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High frequency of neurexin 1β signal peptide structural variants in patients with autism von Feng, Jinong, Schroer, Richard, Yan, Jin, Song, Wenjia, Yang, Chunmei, Bockholt, Anke, Cook, Edwin H., Skinner, Cindy, Schwartz, Charles E., Sommer, Steve S.

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Neurexin 1α structural variants associated with autism von Yan, Jin, Noltner, Katie, Feng, Jinong, Li, Wenyan, Schroer, Richard, Skinner, Cindy, Zeng, Wenqi, Schwartz, Charles E., Sommer, Steve S.

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Duplication of OCRL and adjacent genes associated with autism but not Lowe syndrome von Schroer, Richard J., Beaudet, Arthur L., Shinawi, Marwan, Sahoo, Trilochan, Patel, Ankita, Sun, Qin, Skinner, Cindy, Stevenson, Roger E.

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Autism and macrocephaly von Stevenson, Roger E, Schroer, Richard J, Skinner, Cindy, Fender, Don, Simensen, Richard J

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Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders von Celestino-Soper, Patrícia Bs, Skinner, Cindy, Schroer, Richard, Eng, Patricia, Shenai, Jayant, Nowaczyk, Malgorzata Mj, Terespolsky, Deborah, Cushing, Donna, Patel, Gayle S, Immken, Ladonna, Willis, Alecia, Wiszniewska, Joanna, Matalon, Reuben, Rosenfeld, Jill A, Stevenson, Roger E, Kang, Sung-Hae L, Cheung, Sau Wai, Beaudet, Arthur L, Stankiewicz, Pawel

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Analysis of the neuroligin 4Y gene in patients with autism von Yan, Jin, Feng, Jinong, Schroer, Richard, Li, Wenyan, Skinner, Cindy, Schwartz, Charles E, Cook, Jr, Edwin H, Sommer, Steve S

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Absence of MeCP2 mutations in patients from the South Carolina autism project von Lobo-Menendez, Fe, Sossey-Alaoui, Khalid, Bell, Jennifer M., Copeland-Yates, Susan A., Plank, Sara M., Sanford, Stewart O., Skinner, Cindy, Simensen, Richard J., Schroer, Richard J., Michaelis, Ron C.

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Neurexin 1alpha structural variants associated with autism von Yan, Jin, Noltner, Katie, Feng, Jinong, Li, Wenyan, Schroer, Richard, Skinner, Cindy, Zeng, Wenqi, Schwartz, Charles E, Sommer, Steve S

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High frequency of neurexin 1beta signal peptide structural variants in patients with autism von Feng, Jinong, Schroer, Richard, Yan, Jin, Song, Wenjia, Yang, Chunmei, Bockholt, Anke, Cook, Jr, Edwin H, Skinner, Cindy, Schwartz, Charles E, Sommer, Steve S

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A recurrent 15ql3.3 microdeletion syndrome associated with mental retardation and seizures von SHARP, Andrew J, MEFFORD, Heather C, BROOMER, Adam, CASUGA, Iris, YU WANG, CHUNLIN XIAO, BARBACIORU, Catalin, GIMELLI, Giorgio, DALLA BERNARDINA, Bernardo, TORNIERO, Claudia, GIORDA, Roberto, REGAN, Regina, LI, Kelly, MURDAY, Victoria, MANSOUR, Sahar, FICHERA, Marco, CASTIGLIA, Lucia, FAIFLA, Pinella, VENTURA, Mario, ZHAOSHI JIANG, COOPER, Gregory M, KNIGHT, Samantha J. L, ROMANO, Corrado, BAKER, Carl, ZUFFARDI, Orsetta, CAIFU CHEN, SCHWARTZ, Charles E, EICHLER, Evan E, SKINNER, Cindy, STEVENSON, Roger E, SCHROER, Richard J, NOVARA, Francesca, DE GREGORI, Manuela, CICCONE, Roberto

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The HOPA Gene Dodecamer Duplication Is Not a Significant Etiological Factor in Autism von Michaelis, Ron C, Copeland-Yates, Susan A, Sossey-Alaoui, Khalid, Skinner, Cindy, Friez, Michael J, Longshore, John W, Simensen, Richard J, Schroer, Richard J, Stevenson, Roger E

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Autism and maternally derived aberrations of chromosome 15q von Schroer, Richard J., Phelan, Mary C., Michaelis, Ron C., Crawford, Eric C., Skinner, Steven A., Cuccaro, Michael, Simensen, Richard J., Bishop, Janet, Skinner, Cindy, Fender, Don, Stevenson, Roger E.

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Duplication of OCRL and adjacent genes associated with autism but not Lowe syndrome von Schroer, Richard J., Beaudet, Arthur L., Shinawi, Marwan, Sahoo, Trilochan, Patel, Ankita, Sun, Qin, Skinner, Cindy, Stevenson, Roger E.

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Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism von Plank, Sara M., Copeland-Yates, Susan A., Sossey-Alaoui, Khalid, Bell, Jennifer M., Schroer, Richard J., Skinner, Cindy, Michaelis, Ron C.

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