Small players with a big role: MicroRNAs in pathophysiology of cleft lip and palate

Por Radhakrishna, Uppala
Publicado em 2012

Deep Learning/Artificial Intelligence and Blood-Based DNA Epigenomic Prediction of Cerebral Palsy

Por Bahado-Singh, Ray O., Vishweswaraiah, Sangeetha, Aydas, Buket, Mishra, Nitish Kumar, Guda, Chittibabu, Radhakrishna, Uppala
Publicado no Int J Mol Sci (2019)

Genome-Wide DNA Methylation Analysis and Epigenetic Variations Associated with Congenital Aortic Valve Stenosis (AVS)

Por Radhakrishna, Uppala, Albayrak, Samet, Alpay-Savasan, Zeynep, Zeb, Amna, Turkoglu, Onur, Sobolewski, Paul, Bahado-Singh, Ray O.
Publicado no PLoS One (2016)

Clinical implications of novel activating EGFR mutations in malignant peritoneal mesothelioma

Por Gatalica Zoran, Carreau Joseph H, Govindarajan Venkatesh, Radhakrishna Uppala, Foster Jason M, Sharma Poonam, Nath Swapan K, Loggie Brian W
Publicado em 2010-10-01

Clinical implications of novel activating EGFR mutations in malignant peritoneal mesothelioma

Por Foster, Jason M, Radhakrishna, Uppala, Govindarajan, Venkatesh, Carreau, Joseph H, Gatalica, Zoran, Sharma, Poonam, Nath, Swapan K, Loggie, Brian W
Publicado em 2010

Identification of novel suggestive loci for high-grade myopia in Polish families

Por Rydzanicz, Malgorzata, Nath, Swapan K., Sun, Celi, Podfigurna-Musielak, Monika, Frajdenberg, Agata, Mrugacz, Malgorzata, Winters, Daniel, Ratnamala, Uppala, Radhakrishna, Uppala, Bejjani, Bassem A., Gajecka, Marzena
Publicado em 2011

Newborn blood DNA epigenetic variations and signaling pathway genes associated with Tetralogy of Fallot (TOF)

Por Radhakrishna, Uppala, Vishweswaraiah, Sangeetha, Veerappa, Avinash M., Zafra, Rita, Albayrak, Samet, Sitharam, Prajna H., Saiyed, Nazia M., Mishra, Nitish K., Guda, Chittibabu, Bahado-Singh, Ray
Publicado no PLoS One (2018)

Epigenetically dysregulated genes and pathways implicated in the pathogenesis of non-syndromic high myopia

Por Vishweswaraiah, Sangeetha, Swierkowska, Joanna, Ratnamala, Uppala, Mishra, Nitish K., Guda, Chittibabu, Chettiar, Shiva S., Johar, Kaid R., Mrugacz, Malgorzata, Karolak, Justyna A., Gajecka, Marzena, Radhakrishna, Uppala
Publicado no Sci Rep (2019)

Autosomal Dominant Nonsyndromic Cleft Lip and Palate: Significant Evidence of Linkage at 18q21.1

Por Beiraghi, Soraya , Nath, Swapan K. , Gaines, Matthew , Mandhyan, Desh D. , Hutchings, David , Ratnamala, Uppala , McElreavey, Ken , Bartoloni, Lucia , Antonarakis, Gregory S. , Antonarakis, Stylianos E. , Radhakrishna, Uppala 
Publicado em 2007

Novel homozygous, heterozygous and hemizygous FRMD7 gene mutations segregated in the same consanguineous family with congenital X-linked nystagmus

Por Radhakrishna, Uppala, Ratnamala, Uppala, Deutsch, Samuel, Bartoloni, Lucia, Kuracha, Murali R, Singh, Raminder, Banwait, Jasjit, Bastola, Dhundy K, Johar, Kaid, Nath, Swapan K, Antonarakis, Stylianos E
Publicado em 2012

Genomewide Linkage Scan for Split–Hand/Foot Malformation with Long-Bone Deficiency in a Large Arab Family Identifies Two Novel Susceptibility Loci on Chromosomes 1q42.2-q43 and 6q1...

Por Naveed, Mohammed, Nath, Swapan K., Gaines, Mathew, Al-Ali, Mahmoud T., Al-Khaja, Najib, Hutchings, David, Golla, Jeffrey, Deutsch, Samuel, Bottani, Armand, Antonarakis, Stylianos E., Ratnamala, Uppala, Radhakrishna, Uppala
Publicado em 2007

Localization of a Gene for Keratoconus to a 5.6-Mb Interval on 13q32

Por Gajecka, Marzena, Radhakrishna, Uppala, Winters, Daniel, Nath, Swapan K., Rydzanicz, Malgorzata, Ratnamala, Uppala, Ewing, Kimberly, Molinari, Andrea, Pitarque, Jose A., Lee, Kwanghyuk, Leal, Suzanne M., Bejjani, Bassem A.
Publicado no Invest Ophthalmol Vis Sci (2008)

Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD)

Por Radhakrishna, Uppala, Albayrak, Samet, Zafra, Rita, Baraa, Alosh, Vishweswaraiah, Sangeetha, Veerappa, Avinash M., Mahishi, Deepthi, Saiyed, Nazia, Mishra, Nitish K., Guda, Chittibabu, Ali-Fehmi, Rouba, Bahado-Singh, Ray O.
Publicado no PLoS One (2019)

Y-Chromosome Lineages Trace Diffusion of People and Languages in Southwestern Asia

Por Quintana-Murci, Lluís, Krausz, Csilla, Zerjal, Tatiana, Sayar, S. Hamid, Hammer, Michael F., Mehdi, S. Qasim, Ayub, Qasim, Qamar, Raheel, Mohyuddin, Aisha, Radhakrishna, Uppala, Jobling, Mark A., Tyler-Smith, Chris, McElreavey, Ken
Publicado em 2001

Human Male Infertility Associated with Mutations in NR5A1Encoding Steroidogenic Factor 1

Por Bashamboo, Anu, Ferraz-de-Souza, Bruno, Lourenço, Diana, Lin, Lin, Sebire, Neil J., Montjean, Debbie, Bignon-Topalovic, Joelle, Mandelbaum, Jacqueline, Siffroi, Jean-Pierre, Christin-Maitre, Sophie, Radhakrishna, Uppala, Rouba, Hassan, Ravel, Celia, Seeler, Jacob, Achermann, John C., McElreavey, Ken
Publicado em 2010

Human Male Infertility Associated with Mutations in NR5A1 Encoding Steroidogenic Factor 1

Por Bashamboo, Anu, Ferraz-de-Souza, Bruno, Lourenço, Diana, Lin, Lin, Sebire, Neil J., Montjean, Debbie, Bignon-Topalovic, Joelle, Mandelbaum, Jacqueline, Siffroi, Jean-Pierre, Christin-Maitre, Sophie, Radhakrishna, Uppala, Rouba, Hassan, Ravel, Celia, Seeler, Jacob, Achermann, John C., McElreavey, Ken
Publicado em 2010

Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele

Por Radhakrishna, Uppala, Nath, Swapan K, McElreavey, Ken, Ratnamala, Uppala, Sun, Celi, Maiti, Amit K, Gagnebin, Maryline, Béna, Frédérique, Newkirk, Heather L, Sharp, Andrew J, Everman, David B, Murray, Jeffrey C, Schwartz, Charles E, Antonarakis, Stylianos E, Butler, Merlin G
Publicado no J Med Genet (2012)

Genomewide Scan for Nonsyndromic Cleft Lip and Palate in Multigenerational Indian Families Reveals Significant Evidence of Linkage at 13q33.1-34

Por Radhakrishna, Uppala, Ratnamala, Uppala, Gaines, Mathew, Beiraghi, Soraya, Hutchings, David, Golla, Jeffrey, Husain, Syed A., Gambhir, Prakash S., Sheth, Jayesh J., Sheth, Frenny J., Chetan, Ghati K., Naveed, Mohammed, Solanki, Jitendra V., Patel, Uday C., Master, Dilipkumar C., Memon, Rafiq, Antonarakis, Gregory S., Antonarakis, Stylianos E., Nath, Swapan K.
Publicado em 2006

Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder

Por Segurado, Ricardo, Detera-Wadleigh, Sevilla D., Levinson, Douglas F., Lewis, Cathryn M., Gill, Michael, Nurnberger, Jr., John I., Craddock, Nick, DePaulo, J. Raymond, Baron, Miron, Gershon, Elliot S., Ekholm, Jenny, Cichon, Sven, Turecki, Gustavo, Claes, Stephan, Kelsoe, John R., Schofield, Peter R., Badenhop, Renee F., Morissette, J., Coon, Hilary, Blackwood, Douglas, McInnes, L. Alison, Foroud, Tatiana, Edenberg, Howard J., Reich, Theodore, Rice, John P., Goate, Alison, McInnis, Melvin G., McMahon, Francis J., Badner, Judith A., Goldin, Lynn R., Bennett, Phil, Willour, Virginia L., Zandi, Peter P., Liu, Jianjun, Gilliam, Conrad, Juo, Suh-Hang, Berrettini, Wade H., Yoshikawa, Takeo, Peltonen, Leena, Lönnqvist, Jouko, Nöthen, Markus M., Schumacher, Johannes, Windemuth, Christine, Rietschel, Marcella, Propping, Peter, Maier, Wolfgang, Alda, Martin, Grof, Paul, Rouleau, Guy A., Del-Favero, Jurgen, Van Broeckhoven, Christine, Mendlewicz, Julien, Adolfsson, Rolf, Spence, M. Anne, Luebbert, Hermann, Adams, Linda J., Donald, Jennifer A., Mitchell, Philip B., Barden, Nicholas, Shink, Eric, Byerley, William, Muir, Walter, Visscher, Peter M., Macgregor, Stuart, Gurling, Hugh, Kalsi, Gursharan, McQuillin, Andrew, Escamilla, Michael A., Reus, Victor I., Leon, Pedro, Freimer, Nelson B., Ewald, Henrik, Kruse, Torben A., Mors, Ole, Radhakrishna, Uppala, Blouin, Jean-Louis, Antonarakis, Stylianos E., Akarsu, Nurten
Publicado em 2003