The primacy of NF1 loss as the driver of tumorigenesis in neurofibromatosis type 1-associated plexiform neurofibromas by Pemov, A, Li, H, Patidar, R, Hansen, N F, Sindiri, S, Hartley, S W, Wei, J S, Elkahloun, A, Chandrasekharappa, S C, Boland, J F, Bass, S, Mullikin, J C, Khan, J, Widemann, B C, Wallace, M R, Stewart, D R

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DNA analysis with multiplex microarray-enhanced PCR by Pemov, A., Modi, H., Chandler, D. P., Bavykin, S.

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Attachment to the Nuclear Matrix Mediates Specific Alterations in Chromatin Structure by Pemov, Alexander, Bavykin, Sergei, Hamlin, Joyce L.

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A Potential Role for Mini-chromosome Maintenance (MCM) Proteins in Initiation at the Dihydrofolate Reductase Replication Origin by Alexandrow, Mark G., Ritzi, Marion, Pemov, Alexander, Hamlin, Joyce L.

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Proximal and Long-Range Alterations in Chromatin Structure Surrounding the Chinese Hamster Dihydrofolate Reductase Promoter by Pemov, Alexander, Bavykin, Sergei, Hamlin, Joyce L

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Reliability tests of electric submersible pumps by Belen'kii, P. A., Pemov, Yu. A., Rabotnikov, G. M., Anop, A. A.

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Electrical pumps for iodide-bromide water by Pemov, Yu. A., Khimach, B. V., Gurevich, I. S., Kazakov, Yu. A., Anosov, S. A.

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Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomas by Pemov, Alexander, Dewan, Ramita, Hansen, Nancy F., Chandrasekharappa, Settara C., Ray-Chaudhury, Abhik, Jones, Kristine, Luo, Wen, Heiss, John D., Mullikin, James C., Chittiboina, Prashant, Stewart, Douglas R., Asthagiri, Ashok R.

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Genetics of human malignant peripheral nerve sheath tumors by Pemov, Alexander, Li, Hua, Presley, William, Wallace, Margaret R, Miller, David T

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Collection of Materials from a Seminar Conference on Reliability by Bandyk,I. A, Belenkii,N. A, Pishkov,V. S, Pemov,Yu. A

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Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define premalignant neurofibromatosis type 1-associated atypical neurofibromas by Pemov, Alexander, Hansen, Nancy F, Sindiri, Sivasish, Patidar, Rajesh, Higham, Christine S, Dombi, Eva, Miettinen, Markku M, Fetsch, Patricia, Brems, Hilde, Chandrasekharappa, Settara C, Jones, Kristine, Zhu, Bin, Wei, Jun S, Mullikin, James C, Wallace, Margaret R, Khan, Javed, Legius, Eric, Widemann, Brigitte C, Stewart, Douglas R

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In search of genetic factors predisposing to familial hairy cell leukemia (HCL): exome-sequencing of four multiplex HCL pedigrees by Pemov, Alexander, Pathak, Anand, Jones, Samantha J., Dewan, Ramita, Merberg, Jessica, Karra, Sirisha, Kim, Jung, Arons, Evgeny, Ravichandran, Sarangan, Luke, Brian T., Suman, Shalabh, Yeager, Meredith, Dyer, Martin J. S., Lynch, Henry T., Greene, Mark H., Caporaso, Neil E., Kreitman, Robert J., Goldin, Lynn R., Spinelli, John J., Brooks-Wilson, Angela, McMaster, Mary L., Stewart, Douglas R.

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Glomus Tumors in Neurofibromatosis Type 1: Genetic, Functional, and Clinical Evidence of a Novel Association by BREMS, Hilde, PARK, Caroline, SLOAN, Jennifer L, YAO, Lawrence, LEE, Chyi-Chia Richard, SCIOT, Raf, DE SMET, Luc, LEGIUS, Eric, STEWART, Douglas R, MAERTENS, Ophélia, PEMOV, Alexander, MESSIA, Ludwine, UPADHYAYA, Meena, CLAES, Kathleen, BEERT, Eline, PEETERS, Kristel, MAUTNER, Victor

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Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family by Pathak, Anand, Seipel, Katja, Pemov, Alexander, Dewan, Ramita, Brown, Christina, Ravichandran, Sarangan, Luke, Brian T, Malasky, Michael, Suman, Shalabh, Yeager, Meredith, Gatti, Richard A, Caporaso, Neil E, Mulvihill, John J, Goldin, Lynn R, Pabst, Thomas, McMaster, Mary L, Stewart, Douglas R

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Steels for Bridge Structures by Morozov, Yu. D., Pemov, I. F., Matrosov, M. Yu, Zin’ko, B. F.

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Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis by Pemov, Alexander, Sung, Heejong, Hyland, Paula L, Sloan, Jennifer L, Ruppert, Sarah L, Baldwin, Andrea M, Boland, Joseph F, Bass, Sara E, Lee, Hyo Jung, Jones, Kristine M, Zhang, Xijun, Mullikin, James C, Widemann, Brigitte C, Wilson, Alexander F, Stewart, Douglas R

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Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disorders by Stewart, Douglas R, Pemov, Alexander, Johnston, Jennifer J, Sapp, Julie C, Yeager, Meredith, He, Ji, Boland, Joseph F, Burdett, Laurie, Brown, Christina, Gatti, Richard A, Alter, Blanche P, Biesecker, Leslie G, Savage, Sharon A

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Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls by Kim, Jung, Luo, Wen, Wang, Mingyi, Wegman-Ostrosky, Talia, Frone, Megan N, Johnston, Jennifer J, Nickerson, Michael L, Rotunno, Melissa, Li, Shengchao A, Achatz, Maria I, Brodie, Seth A, Dean, Michael, de Andrade, Kelvin C, Fortes, Fernanda P, Gianferante, Matthew, Khincha, Payal, McMaster, Mary L, McReynolds, Lisa J, Pemov, Alexander, Pinheiro, Maisa, Santiago, Karina M, Alter, Blanche P, Caporaso, Neil E, Gadalla, Shahinaz M, Goldin, Lynn R, Greene, Mark H, Loud, Jennifer, Yang, Xiaohong R, Freedman, Neal D, Gapstur, Susan M, Gaudet, Mia M, Calista, Donato, Ghiorzo, Paola, Fargnoli, Maria Concetta, Nagore, Eduardo, Peris, Ketty, Puig, Susana, Landi, Maria Teresa, Hicks, Belynda, Zhu, Bin, Liu, Jia, Sampson, Joshua N, Chanock, Stephen J, Mirabello, Lisa J, Morton, Lindsay M, Biesecker, Leslie G, Tucker, Margaret A, Savage, Sharon A, Goldstein, Alisa M, Stewart, Douglas R

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Evidence of polyclonality in neurofibromatosis type 2-associated multilobulated vestibular schwannomas by Dewan, Ramita, Pemov, Alex, Kim, H Jeffrey, Morgan, Keaton L, Vasquez, Raul A, Chittiboina, Prashant, Wang, Xiang, Chandrasekharappa, Settara C, Ray-Chaudhury, Abhik, Butman, John A, Stewart, Douglas R, Asthagiri, Ashok R

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Genome‐wide association study of café‐au‐lait macule number in neurofibromatosis type 1 by Sung, Heejong, Hyland, Paula L., Pemov, Alexander, Sabourin, Jeremy A., Baldwin, Andrea M., Bass, Sara, Teshome, Kedest, Luo, Wen, Widemann, Brigitte C., Stewart, Douglas R., Wilson, Alexander F.

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