Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment
NHO, K, CORNEVEAUX, J. J, INLOW, M. H, SINIARD, A. L, REIMAN, R. A, AISEN, P. S, PETERSEN, R. C, GREEN, R. C, JACK, C. R, WEINER, M. W, BALDWIN, C. T, LUNETTA, K, KIM, S, FARRER, L. A, FUMEY, S. J, LOVESTONE, S, SIMMONS, A, MECOCCI, P, VELLAS, B, TSOLAKI, M, KLOSZEWSKA, I, SOININEN, H, MCDONALD, B. C, LIN, H, FARLOW, M. R, GHETTI, B, HUENTELMAN, M. J, SAYKIN, A. J, RISACHER, S. L, SHEN, L, SWAMINATHAN, S, RAMANAN, V. K, LIU, Y, FOROUD, T
Published in Molecular psychiatry (01.07.2013)
Published in Molecular psychiatry (01.07.2013)
Get full text
Journal Article
apoplastic chitinase CpCHT1 isolated from the corolla of wintersweet exhibits both antifreeze and antifungal activities
Zhang, S. -H, Wei, Y, Liu, J. -L, Yu, H. -M, Yin, J. -H, Pan, H. -Y, Baldwin, T. C
Published in Biologia plantarum (01.03.2011)
Published in Biologia plantarum (01.03.2011)
Get full text
Journal Article
Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics
Nho, K, Corneveaux, J J, Kim, S, Lin, H, Risacher, S L, Shen, L, Swaminathan, S, Ramanan, V K, Liu, Y, Foroud, T, Inlow, M H, Siniard, A L, Reiman, R A, Aisen, P S, Petersen, R C, Green, R C, Jack, C R, Weiner, M W, Baldwin, C T, Lunetta, K, Farrer, L A, Furney, S J, Lovestone, S, Simmons, A, Mecocci, P, Vellas, B, Tsolaki, M, Kloszewska, I, Soininen, H, McDonald, B C, Farlow, M R, Ghetti, B, Huentelman, M J, Saykin, A J
Published in Molecular psychiatry (01.07.2013)
Published in Molecular psychiatry (01.07.2013)
Get full text
Journal Article
Inflammation and metabolism gene sets in subcutaneous abdominal adipose tissue are altered 1 hour after exercise in adults with obesity
Ludzki, A C, Schleh, M W, Krueger, E M, Taylor, N M, Ryan, B J, Baldwin, T C, Gillen, J B, Ahn, C, Varshney, P, Horowitz, J F
Published in Journal of applied physiology (1985) (01.10.2021)
Published in Journal of applied physiology (1985) (01.10.2021)
Get full text
Journal Article
Genetic association between endothelial nitric oxide synthase and Alzheimer disease
Akomolafe, A, Lunetta, KL, Erlich, PM, Cupples, LA, Baldwin, CT, Huyck, M, Green, RC, Farrer, LA
Published in Clinical genetics (01.07.2006)
Published in Clinical genetics (01.07.2006)
Get full text
Journal Article
Maternal component in the familial aggregation of hypertension
DeStefano, AL, Gavras, H, Heard-Costa, N, Bursztyn, M, Manolis, A, Farrer, LA, Baldwin, CT, Gavras, I, Schwartz, F
Published in Clinical genetics (01.07.2001)
Published in Clinical genetics (01.07.2001)
Get full text
Journal Article
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3
BONNE-TAMIR, B, DESTEFANO, A. L, BRIGGS, C. E, ADAIR, R, FRANKLYN, B, WEISS, S, KOROSTISHEVSKY, M, FRYDMAN, M, BALDWIN, C. T, FARRER, L. A
Published in American journal of human genetics (01.06.1996)
Get full text
Published in American journal of human genetics (01.06.1996)
Journal Article
Evidence for Linkage Between Essential Hypertension and a Putative Locus on Human Chromosome 17
Baima, Jader, Nicolaou, Michael, Schwartz, Faina, DeStefano, Anita L, Manolis, Athanasios, Gavras, Irene, Laffer, Cheryl, Elijovich, Fernando, Farrer, Lindsay, Baldwin, Clinton T, Gavras, Haralambos
Published in Hypertension (Dallas, Tex. 1979) (01.07.1999)
Published in Hypertension (Dallas, Tex. 1979) (01.07.1999)
Get full text
Journal Article
BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia
Sebastiani, P., Farrell, J.J., Alsultan, A., Wang, S., Edward, H.L., Shappell, H., Bae, H., Milton, J.N., Baldwin, C.T., Al-Rubaish, A.M., Naserullah, Z., Al-Muhanna, F., Alsuliman, A., Patra, P.K., Farrer, L.A., Ngo, D., Vathipadiekal, V., Chui, D.H.K., Al-Ali, A.K., Steinberg, M.H.
Published in Blood cells, molecules, & diseases (01.03.2015)
Published in Blood cells, molecules, & diseases (01.03.2015)
Get full text
Journal Article
Genetic predisposition to stroke in relatives of hypertensives
NICOLAOU, M, DESTEFANO, A. L, GAVRAS, I, CUPPLES, L. A, MANOLIS, A. J, BALDWIN, C. T, GAVRAS, H, FARRER, L. A
Published in Stroke (1970) (01.02.2000)
Published in Stroke (1970) (01.02.2000)
Get full text
Journal Article
Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea
Ma, Q, Wyszynski, D F, Farrell, J J, Kutlar, A, Farrer, L A, Baldwin, C T, Steinberg, M H
Published in The pharmacogenomics journal (01.12.2007)
Published in The pharmacogenomics journal (01.12.2007)
Get full text
Journal Article
Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia
Wyszynski, D F, Baldwin, C T, Cleves, M A, Amirault, Y, Nolan, V G, Farrell, J J, Bisbee, A, Kutlar, A, Farrer, L A, Steinberg, M H
Published in Cellular and molecular biology (Noisy-le-Grand, France) (01.02.2004)
Get more information
Published in Cellular and molecular biology (Noisy-le-Grand, France) (01.02.2004)
Journal Article
Single Base Mutation in the Type II Procollagen Gene (COL2A1) as a Cause of Primary Osteoarthritis Associated with a Mild Chondrodysplasia
Ala-Kokko, Leena, Baldwin, Clinton T., Moskowitz, Roland W., Prockop, Darwin J.
Published in Proceedings of the National Academy of Sciences - PNAS (01.09.1990)
Published in Proceedings of the National Academy of Sciences - PNAS (01.09.1990)
Get full text
Journal Article
Structure of cDNA clones coding for the entire preproα1 (III) chain of human type III procollagen. Differences in protein structure from type I procollagen and conservation of codon preferences
Ala-Kokko, L, Kontusaari, S, Baldwin, C T, Kuivaniemi, H, Prockop, D J
Published in Biochemical journal (01.06.1989)
Published in Biochemical journal (01.06.1989)
Get full text
Journal Article
Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population
Baldwin, C T, Weiss, S, Farrer, L A, De Stefano, A L, Adair, R, Franklyn, B, Kidd, K K, Korostishevsky, M, Bonné-Tamir, B
Published in Human molecular genetics (01.09.1995)
Published in Human molecular genetics (01.09.1995)
Get more information
Journal Article
Autosomal Dominant Orthostatic Hypotensive Disorder Maps to Chromosome 18q
DeStefano, Anita L., Baldwin, Clinton T., Burzstyn, Michael, Gavras, Irene, Handy, Diane E., Joost, Oscar, Martel, Timothy, Nicolaou, Michael, Schwartz, Faina, Streeten, David H.P., Farrer, Lindsay A., Gavras, Haralambos
Published in American journal of human genetics (01.11.1998)
Published in American journal of human genetics (01.11.1998)
Get full text
Journal Article
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations
DESTEFANO, A. L, CUPPLES, L. A, LALWANI, A. K, MILUNSKY, A, NANCE, W. E, PANDYA, A, RAMESAR, R. S, READ, A. P, TASSABEJHI, M, WILCOX, E. R, FARRER, L. A, ARNOS, K. S, ASHER, J. H, BALDWIN, C. T, BLANTON, S, CAREY, M. L, DA SILVA, E. O, FRIEDMAN, T. B, GREENBERG, J
Published in Human genetics (01.05.1998)
Published in Human genetics (01.05.1998)
Get full text
Journal Article