On the probability that a novel variant is a disease-causing mutation

Por Mitchell, Adele A., Chakravarti, Aravinda, Cutler, David J.
Publicado em 2005

Undetected Genotyping Errors Cause Apparent Overtransmission of Common Alleles in the Transmission/Disequilibrium Test

Por Mitchell, Adele A., Cutler, David J., Chakravarti, Aravinda
Publicado em 2003

Estimating the number of contributors to two-, three-, and four-person mixtures containing DNA in high template and low template amounts

Por Perez, Jaheida, Mitchell, Adele A., Ducasse, Nubia, Tamariz, Jeannie, Caragine, Theresa
Publicado em 2011

Increased Postpartum Thyroxine Replacement in Hashimoto's Thyroiditis

Por Galofré, Juan C., Haber, Richard S., Mitchell, Adele A., Pessah, Rachel, Davies, Terry F.
Publicado em 2010

Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia

Por Sharma, Nutan, Franco, Ramon A, Kuster, John, Mitchell, Adele A., Fuchs, Tania, Saunders-Pullman, Rachel, Raymond, Deborah, Brin, Mitchell F., Blitzer, Andrew, Bressman, Susan B., Ozelius, Laurie J.
Publicado em 2010

Evaluation of 22 genetic variants with Crohn's Disease risk in the Ashkenazi Jewish population: a case-control study

Por Peter, Inga, Mitchell, Adele A, Ozelius, Laurie, Erazo, Monica, Hu, Jianzhong, Doheny, Dana, Abreu, Maria T, Present, Daniel H, Ullman, Thomas, Benkov, Keith, Korelitz, Burton I, Mayer, Lloyd, Desnick, Robert J
Publicado em 2011

Association between the Tumor Necrosis Factor Locus and the Clinical Outcome of Leishmania chagasi Infection

Por Karplus, Theresa M., Jeronimo, Selma M. B., Chang, Haeok, Helms, Bethany K., Burns, Trudy L., Murray, Jeffrey C., Mitchell, Adele A., Pugh, Elizabeth W., Braz, Regina F. S., Bezerra, Fabiana L., Wilson, Mary E.
Publicado em 2002

Microdeletions of 3q29 Confer High Risk for Schizophrenia

Por Mulle, Jennifer Gladys, Dodd, Anne F., McGrath, John A., Wolyniec, Paula S., Mitchell, Adele A., Shetty, Amol C., Sobreira, Nara L., Valle, David, Rudd, M. Katharine, Satten, Glen, Cutler, David J., Pulver, Ann E., Warren, Stephen T.
Publicado em 2010

Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia

Por Mulle, Jennifer Gladys, Pulver, Ann E., McGrath, John M., Wolyniec, Paula, Dodd, Anne F., Cutler, David J., Sebat, Jonathan, Malhotra, Dheeraj, Nestadt, Gerald, Conrad, Donald F., Hurles, Matthew, Barnes, Chris P., Ikeda, Masashi, Iwata, Nakao, Levinson, Douglas F., Gejman, Pablo V., Sanders, Alan R., Duan, Jubao, Mitchell, Adele A., Peter, Inga, Sklar, Pamela, O’Dushlaine, Colm T., Grozeva, Detelina, O’Donovan, Michael C., Owen, Michael J., Hultman, Christina M., Kähler, Anna K., Sullivan, Patrick F., Kirov, George, Warren, Stephen T.
Publicado em 2013

A Genome-Wide Scan of Ashkenazi Jewish Crohn's Disease Suggests Novel Susceptibility Loci

Por Kenny, Eimear E., Pe'er, Itsik, Karban, Amir, Ozelius, Laurie, Mitchell, Adele A., Ng, Sok Meng, Erazo, Monica, Ostrer, Harry, Abraham, Clara, Abreu, Maria T., Atzmon, Gil, Barzilai, Nir, Brant, Steven R., Bressman, Susan, Burns, Edward R., Chowers, Yehuda, Clark, Lorraine N., Darvasi, Ariel, Doheny, Dana, Duerr, Richard H., Eliakim, Rami, Giladi, Nir, Gregersen, Peter K., Hakonarson, Hakon, Jones, Michelle R., Marder, Karen, McGovern, Dermot P. B., Mulle, Jennifer, Orr-Urtreger, Avi, Proctor, Deborah D., Pulver, Ann, Rotter, Jerome I., Silverberg, Mark S., Ullman, Thomas, Warren, Stephen T., Waterman, Matti, Zhang, Wei, Bergman, Aviv, Mayer, Lloyd, Katz, Seymour, Desnick, Robert J., Cho, Judy H., Peter, Inga
Publicado em 2012