A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any Age by AHSAN, Habibul, HALPERN, Jerry, ROY, Shantanu, BRUTUS, Rachelle, ARGOS, Maria, MELKONIAN, Stephanie, CHANG-CLAUDE, Jenny, ANDRULIS, Irene, HOPPER, John L, JOHN, Esther M, MALONE, Kathi, URSIN, Giske, KIBRIYA, Muhammad G, GAMMON, Marilie D, THOMAS, Duncan C, SEMINARA, Daniela, CASEY, Graham, KNIGHT, Julia A, SOUTHEY, Melissa C, GILES, Graham G, SANTELLA, Regina M, EUNJUNG LEE, CONTI, David, PIERCE, Brandon L, DUGGAN, David, GALLINGER, Steve, HAILE, Robert, JENKINS, Mark, LINDOR, Noralane M, NEWCOMB, Polly, MICHAILIDOU, Kyriaki, APICELLA, Carmel, PARK, Daniel J, PETO, Julian, LIN TONG, FLETCHER, Olivia, DOS SANTOS SILVA, Isabel, LATHROP, Mark, HUNTER, David J, CHANOCK, Stephen J, MEINDL, Alfons, SCHMUTZLER, Rita K, MÜLLER-MYHSOK, Bertram, LOCHMANN, Magdalena, BECKMANN, Lars, GAMAZON, Eric, HEIN, Rebecca, MAKALIC, Enes, SCHMIDT, Daniel F, QUANG MINH BUI, STONE, Jennifer, FLESCH-JANYS, Dieter, DAHMEN, Norbert, NEVANLINNA, Heli, AITTOMÄKI, Kristiina, BLOMQVIST, Carl, MCGUIRE, Valerie, FELBERG, Anna, JIANXIN SHI, JASMINE, Farzana

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Growth in stature and head circumference in high-functioning autism and Asperger disorder during the first 3 years of life by DISSANAYAKE, CHERYL, BUI, QUANG M., HUGGINS, RICHARD, LOESCH, DANUTA Z.

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Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism by Loesch, DZ, Khaniani, MS, Slater, HR, Rubio, JP, Bui, QM, Kotschet, K, D'Souza, W, Venn, A, Kalitsis, P, Choo, AKH, Burgess, T, Johnson, L, Evans, A, Horne, M

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Effect of the Fragile X Status Categories and the Fragile X Mental Retardation Protein Levels on Executive Functioning in Males and Females With Fragile X by Loesch, Danuta Z, Bui, Quang M, Grigsby, Jim, Butler, Emma, Epstein, Jennifer, Huggins, Richard M, Taylor, Annette K, Hagerman, Randi J

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The effects of mode of exercise instruction on compliance with a home exercise program in older adults with osteoarthritis by Schoo, A.M.M., Morris, M.E., Bui, Q.M.

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Effect of Turner's syndrome and X-linked imprinting on cognitive status: analysis based on pedigree data by Loesch, Danuta Z., Bui, Quang Minh, Kelso, Wendy, Huggins, Richard M., Slater, Howard, Warne, Garry, Bergman, Paul, Rodda, Christine, Mitchell, Robert John, Prior, Margot

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Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis by Loesch, D.Z., Huggins, R.M., Bui, Q.M., Taylor, A.K., Pratt, C., Epstein, J., Hagerman, R.J.

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Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: A new perspective by Loesch, D.Z., Huggins, R.M., Bui, Q. M., Taylor, A. K., Hagerman, R. J.

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Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile-X by Huggins, R.M., Loesch, D.Z., Qian, G.Q., Bui, Q.M., Mitchell, R.J., Dobson, M., Taylor, A.K.

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Inference for the random coefficients bifurcating autoregressive model for cell lineage studies by Bui, Q.M, Huggins, R.M

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Robust Inference for the Bivariate Bifurcating Autoregressive Model by Bui, Quang M., Huggins, Richard M.

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A case of self‐improving collodion ichthyosis in Vietnam by Diep, Quang Minh, Luong, Long Hoang, Tran, Thinh Huy, Dinh, Oanh Thi Lan, Nguyen, Hung Quoc, Bui, The‐Hung, Ta, Thanh Van, Tran, Van Khanh

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Microcephaly primary hereditary (MCPH): Report of novel ASPM variants and prenatal diagnosis in a Vietnamese family by Tran, Thinh Huy, Diep, Quang Minh, Cao, My Ha, Luong, Long Hoang, Pham, Van Anh, Lan Dinh, Oanh Thi, Bui, The-Hung, Van Ta, Thanh, Tran, Van Khanh

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Whole exome sequencing analysis in a couple with three children who died prematurely due to carnitine-acylcarnitine translocase deficiency by Tran, Van Khanh, Diep, Quang Minh, Qiu, Zilong, Le, Thi Phuong, Do, Long Duy, Tran, Hai Anh, Bui, The-Hung, Ta, Thanh Van, Tran, Thinh Huy

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