Fingerprint Fingerprint is based on mining the text of the persons scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 4 Similar Profiles
DNA Methylation Medicine & Life Sciences
Epigenomics Medicine & Life Sciences
Methylation Medicine & Life Sciences
Gene Expression Medicine & Life Sciences
Genome Medicine & Life Sciences
Genes Medicine & Life Sciences
Neoplasms Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences

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Research Output 2001 2018

Genome-wide DNA methylation associations with spontaneous preterm birth in US blacks: findings in maternal and cord blood samples

Hong, X., Sherwood, B., Ladd-Acosta, C., Peng, S., Ji, H., Hao, K., Burd, I., Bartell, T. R., Wang, G., Tsai, H. J., Liu, X., Ji, Y., Wahl, A., Caruso, D., Lee-Parritz, A., Zuckerman, B. & Wang, X. Mar 1 2018 (Accepted/In press) In : Epigenetics. p. 1-10 10 p.

Research output: Contribution to journalArticle

Premature Birth
DNA Methylation
Fetal Blood
Mothers
Genome

In silico epigenetics of metal exposure and subclinical atherosclerosis in middle aged men: Pilot results from the aragon workers health study

Riffo-Campos, A. L., Fuentes-Trillo, A., Tang, W. Y., Soriano, Z., De Marco, G., Rentero-Garrido, P., Adam-Felici, V., Lendinez-Tortajada, V., Francesconi, K., Goessler, W., Ladd-Acosta, C., Leon-Latre, M., Casasnovas, J. A., Chaves, F. J., Navas-Acien, A., Guallar, E. & Tellez-Plaza, M. Jun 5 2018 In : Philosophical Transactions of the Royal Society B: Biological Sciences. 373, 1748, 20170084

Research output: Contribution to journalArticle

middle-aged adults
health care workers
atherosclerosis
Epigenomics
epigenetics

Integrating RNA Expression Identifies Candidate Gene for Orofacial Clefts

Ladd-Acosta, C. & Beaty, T. H. Jan 1 2018 In : Journal of Dental Research. 97, 1, p. 31-32 2 p.

Research output: Contribution to journalArticle

Cleft Lip
Cleft Palate
Genomics
RNA
Gene Expression

Cross-tissue integration of genetic and epigenetic data offers insight into autism spectrum disorder

Andrews, S. V., Ellis, S. E., Bakulski, K. M., Sheppard, B., Croen, L. A., Hertz-Picciotto, I., Newschaffer, C. J., Feinberg, A. P., Arking, D. E., Ladd-Acosta, C. & Fallin, M. D. Dec 1 2017 In : Nature Communications. 8, 1, 1011

Research output: Contribution to journalArticle

methylation
Epigenomics
DNA Methylation
Blood
blood

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Anney, R. J. L. , Ripke, S. , Anttila, V. , Grove, J. , Holmans, P. , Huang, H. , Klei, L. , Lee, P. H. , Medland, S. E. , Neale, B. , Robinson, E. , Weiss, L. A. , Zwaigenbaum, L. , Yu, T. W. , Wittemeyer, K. , Willsey, A. J. , Wijsman, E. M. , Werge, T. , Wassink, T. H. , Waltes, R. & 143 others Walsh, C. A., Wallace, S., Vorstman, J. A. S., Vieland, V. J., Vicente, A. M., Vanengeland, H., Tsang, K., Thompson, A. P., Szatmari, P., Svantesson, O., Steinberg, S., Stefansson, K., Stefansson, H., State, M. W., Soorya, L., Silagadze, T., Scherer, S. W., Schellenberg, G. D., Sandin, S., Sanders, S. J., Saemundsen, E., Rouleau, G. A., Rogé, B., Roeder, K., Roberts, W., Reichert, J., Reichenberg, A., Rehnström, K., Regan, R., Poustka, F., Poultney, C. S., Piven, J., Pinto, D., Pericak-Vance, M. A., Pejovic-Milovancevic, M., Pedersen, M. G., Pedersen, C. B., Paterson, A. D., Parr, J. R., Pagnamenta, A. T., Oliveira, G., Nurnberger, J. I., Nordentoft, M., Murtha, M. T., Mouga, S., Mortensen, P. B., Mors, O., Morrow, E. M., Moreno-De-Luca, D., Monaco, A. P., Minshew, N., Merikangas, A., McMahon, W. M., McGrew, S. G., Mattheisen, M., Martsenkovsky, I., Martin, D. M., Mane, S. M., Magnusson, P., Magalhaes, T., Maestrini, E., Lowe, J. K., Lord, C., Levitt, P., Martin, C. L., Ledbetter, D. H., Leboyer, M., Lecouteur, A. S., Ladd-Acosta, C., Kolevzon, A., Klauck, S. M., Jacob, S., Iliadou, B., Hultman, C. M., Hougaard, D. M., Hertz-Picciotto, I., Hendren, R., Hansen, C. S., Haines, J. L., Guter, S. J., Grice, D. E., Green, J. M., Green, A., Goldberg, A. P., Gillberg, C., Gilbert, J., Gallagher, L., Freitag, C. M., Fombonne, E., Folstein, S. E., Fernandez, B., Fallin, M. D., Ercan-Sencicek, A. G., Ennis, S., Duque, F., Duketis, E., Delorme, R., Derubeis, S., Dejonge, M. V., Dawson, G., Cuccaro, M. L., Correia, C. T., Conroy, J., Conceição, I. C., Chiocchetti, A. G., Celestino-Soper, P. B. S., Casey, J., Cantor, R. M., Café, C., Bybjerg-Grauholm, J., Brennan, S., Bourgeron, T., Bolton, P. F., Bölte, S., Bolshakova, N., Betancur, C., Bernier, R., Beaudet, A. L., Battaglia, A., Bal, V. H., Baird, G., Bailey, A. J., Bækvad-Hansen, M., Bader, J. S., Bacchelli, E., Anagnostou, E., Amaral, D., Almeida, J., Børglum, A. D., Buxbaum, J. D., Chakravarti, A., Cook, E. H., Coon, H., Geschwind, D. H., Gill, M., Hallmayer, J., Palotie, A., Santangelo, S., Sutcliffe, J. S., Arking, D. E., Devlin, B., Daly, M. J. & Hakonarson, H. May 22 2017 In : Molecular Autism. 8, 1, 21

Research output: Contribution to journalArticle

Genome-Wide Association Study
Meta-Analysis
Schizophrenia
Genome
Genomics