Items where Author is "Krithika, S."

Journal Article

Cioclu, Maria C., Coppola, Antonietta, Tondelli, Manuela, Vaudano, Anna E., Giovannini, Giada, Krithika, S., Iacomino, Michele, Zara, Federico, Sisodiya, Sanjay M. and Meletti, Stefano (2021) Cortical and Subcortical Network Dysfunction in a Female Patient With NEXMIF Encephalopathy. Frontiers in Neurology, 12. p. 722664. ISSN 1664-2295

Zagaglia, Sara, Steel, Dora, Krithika, S., Hernandez-Hernandez, Laura, Custodio, Helena M., Gorman, Kathleen M., Vezyroglou, Aikaterini, Møller, Rikke S., King, Mary D., Hammer, Trine B., Spaull, Robert, Fazeli, Walid, Bartolomaeus, Tobias, Doummar, Diane, Keren, Boris, Mignot, Cyril, Bednarek, Nathalie, Cross, J. Helen, Mallick, Andrew A., Sanchis-Juan, Alba, Basu, Anna, Raymond, F. Lucy, Lynch, Bryan J., Majumdar, Anirban, Stamberger, Hannah, Weckhuysen, Sarah, Sisodiya, Sanjay M. and Kurian, Manju A. (2021) RHOBTB2 mutations expand the phenotypic spectrum of alternating hemiplegia of childhood. Neurology. ISSN 1526-632X

Coppola, Antonietta, Hernandez-Hernandez, Laura, Balestrini, Simona, Krithika, S., Moran, Nicholas, Hale, Blake, Cordivari, Carla and Sisodiya, Sanjay M. (2020) Cortical myoclonus and epilepsy in a family with a new SLC20A2 mutation. Journal of Neurology, 267 (8). pp. 2221-2227. ISSN 1432-1459

Johannesen, Katrine M., Gardella, Elena, Encinas, Alejandra C., Lehesjoki, Anna‐Elina, Linnankivi, Tarja, Petersen, Michael B., Lund, Ida C. B., Blichfeldt, Susanne, Miranda, Maria J., Pal, Deb K., Lascelles, Karine, Procopis, Peter, Orsini, Alessandro, Bonuccelli, Alice, Giacomini, Thea, Helbig, Ingo, Fenger, Christina D., Sisodiya, Sanjay M., Hernandez‐Hernandez, Laura, Krithika, S., Rumple, Melissa, Masnada, Silvia, Valente, Marialuisa, Cereda, Cristina, Giordano, Lucio, Accorsi, Patrizia, Bürki, Sarah E., Mancardi, Margherita, Korff, Christian, Guerrini, Renzo, Spiczak, Sarah, Hoffman‐Zacharska, Dorota, Mazurczak, Tomasz, Coppola, Antonietta, Buono, Salvatore, Vecchi, Marilena, Hammer, Michael F., Varesio, Costanza, Veggiotti, Pierangelo, Lal, Dennis, Brünger, Tobias, Zara, Federico, Striano, Pasquale, Rubboli, Guido and Møller, Rikke S. (2019) The spectrum of intermediate SCN 8A ‐related epilepsy. Epilepsia, 60 (5). pp. 830-844. ISSN 1528-1167

Baldassari, Sara, Picard, Fabienne, Verbeek, Nienke E., van Kempen, Marjan, Brilstra, Eva H., Lesca, Gaetan, Conti, Valerio, Guerrini, Renzo, Bisulli, Francesca, Licchetta, Laura, Pippucci, Tommaso, Tinuper, Paolo, Hirsch, Edouard, de Saint Martin, Anne, Chelly, Jamel, Rudolf, Gabrielle, Chipaux, Mathilde, Ferrand-Sorbets, Sarah, Dorfmüller, Georg, Sisodiya, Sanjay, Balestrini, Simona, Schoeler, Natasha, Hernandez-Hernandez, Laura, Krithika, S., Oegema, Renske, Hagebeuk, Eveline, Gunning, Boudewijn, Deckers, Charles, Berghuis, Bianca, Wegner, Ilse, Niks, Erik, Jansen, Floor E., Braun, Kees, de Jong, Daniëlle, Rubboli, Guido, Talvik, Inga, Sander, Valentin, Uldall, Peter, Jacquemont, Marie-Line, Nava, Caroline, Leguern, Eric, Julia, Sophie, Gambardella, Antonio, d’Orsi, Giuseppe, Crichiutti, Giovanni, Faivre, Laurence, Darmency, Veronique, Benova, Barbora, Krsek, Pavel, Biraben, Arnaud, Lebre, Anne-Sophie, Jennesson, Mélanie, Sattar, Shifteh, Marchal, Cécile, Nordli, Douglas R., Lindstrom, Kristin, Striano, Pasquale, Lomax, Lysa B., Kiss, Courtney, Bartolomei, Fabrice, Lepine, Anne F., Schoonjans, An-Sofie, Stouffs, Katrien, Jansen, Anna, Panagiotakaki, Eleni, Ricard-Mousnier, Brigitte, Thevenon, Julien, de Bellescize, Julitta, Catenoix, Hélène, Dorn, Thomas, Zenker, Martin, Müller-Schlüter, Karen, Brandt, Christian, Krey, Ilona, Polster, Tilman, Wolff, Markus, Balci, Meral, Rostasy, Kevin, Achaz, Guillaume, Zacher, Pia, Becher, Thomas, Cloppenborg, Thomas, Yuskaitis, Christopher J., Weckhuysen, Sarah, Poduri, Annapurna, Lemke, Johannes R., Møller, Rikke S. and Baulac, Stéphanie (2019) The landscape of epilepsy-related GATOR1 variants. Genetics in Medicine, 21 (2). pp. 398-408. ISSN 1530-0366

Zagaglia, Sara, Selch, Christina, Nisevic, Jelena R., Mei, Davide, Michalak, Zuzanna, Hernandez-Hernandez, Laura, Krithika, S., Vezyroglou, Katharina, Varadkar, Sophia M., Pepler, Alexander, Biskup, Saskia, Leão, Miguel, Gärtner, Jutta, Merkenschlager, Andreas, Jaksch, Michaela, Møller, Rikke S., Gardella, Elena, Kristiansen, Britta S., Hansen, Lars K., Vari, Maria S., Helbig, Katherine L., Desai, Sonal, Smith-Hicks, Constance L., Hino-Fukuyo, Naomi, Talvik, Tiina, Laugesaar, Rael, Ilves, Pilvi, Õunap, Katrin, Körber, Ingrid, Hartlieb, Till, Kudernatsch, Manfred, Winkler, Peter, Schimmel, Mareike, Hasse, Anette, Knuf, Markus, Heinemeyer, Jan, Makowski, Christine, Ghedia, Sondhya, Subramanian, Gopinath M., Striano, Pasquale, Thomas, Rhys H., Micallef, Caroline, Thom, Maria, Werring, David J., Kluger, Gerhard J., Cross, J. Helen, Guerrini, Renzo, Balestrini, Simona and Sisodiya, Sanjay M. (2018) Neurologic phenotypes associated with COL4A1/2 mutations. Neurology, 91 (22). e2078-e2088. ISSN 1526-632X

Coppola, Antonietta, Morrogh, Deborah, Farrell, Fiona, Balestrini, Simona, Hernandez-Hernandez, Laura, Krithika, S., Sander, Josemir W., Waters, Jonathan J. and Sisodiya, Sanjay M. (2018) Ring Chromosome 17 Not Involving the Miller-Dieker Region: A Case with Drug-Resistant Epilepsy. Molecular Syndromology, 9 (1). pp. 38-44. ISSN 1661-8777

Rawofi, Lida, Edwards, Melissa, Krithika, S., Le, Phuong, Cha, David, Yang, Zhaohui, Ma, Yanyun, Wang, Jiucun, Su, Bing, Jin, Li, Norton, Heather L. and Parra, Esteban J. (2017) Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry. PeerJ, 5. e3951. ISSN 2167-8359

Norton, Heather L., Edwards, Melissa, Krithika, S., Johnson, Monique, Werren, Elizabeth A. and Parra, Esteban J. (2016) Quantitative assessment of skin, hair, and iris variation in a diverse sample of individuals and associated genetic variation. American Journal of Physical Anthropology, 160 (4). pp. 570-581. ISSN 1096-8644

Edwards, Melissa, Cha, David, Krithika, S., Johnson, Monique, Cook, Gillian and Parra, Esteban J. (2016) Iris pigmentation as a quantitative trait: variation in populations of European, East Asian and South Asian ancestry and association with candidate gene polymorphisms. Pigment Cell and Melanoma Research, 29 (2). pp. 141-162. ISSN 1755-148X

Below, Jennifer E., Parra, Esteban J., Gamazon, Eric R., Torres, Jason, Krithika, S., Candille, Sophie, Lu, Yingchang, Manichakul, Ani, Peralta-Romero, Jesus, Duan, Qing, Li, Yun, Morris, Andrew P., Gottesman, Omri, Bottinger, Erwin, Wang, Xin-Qun, Taylor, Kent D., Ida Chen, Y.-D., Rotter, Jerome I., Rich, Stephen S., Loos, Ruth J. F., Tang, Hua, Cox, Nancy J., Cruz, Miguel, Hanis, Craig L. and Valladares-Salgado, Adan (2016) Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects and tissue-specific enrichment of eQTLs. Scientific Reports, 6 (1). p. 19429. ISSN 2045-2322

Edwards, Melissa, Cha, David, Krithika, S., Johnson, Monique and Parra, Esteban J. (2016) Analysis of iris surface features in populations of diverse ancestry. Royal Society Open Science, 3 (1). p. 150424. ISSN 2054-5703

Parra, Esteban J., Botton, Mariana R., Perini, Jamila A., Krithika, S., Bourgeois, Stephane, Johnson, Todd A., Tsunoda, Tatsuhiko, Pirmohamed, Munir, Wadelius, Mia, Limdi, Nita A., Cavallari, Larisa H., Burmester, James K., Rettie, Allan E., Klein, Teri E., Johnson, Julie A., Hutz, Mara H. and Suarez-Kurtz, Guilherme (2015) Genome-wide association study of warfarin maintenance dose in a Brazilian sample. Pharmacogenomics, 16 (11). pp. 1253-1263. ISSN 1744-8042

Eaton, Katherine, Edwards, Melissa, Krithika, S., Cook, Gillian, Norton, Heather and Parra, Esteban J. (2015) Association study confirms the role of two OCA2 polymorphisms in normal skin pigmentation variation in East Asian populations. American Journal of Human Biology, 27 (4). pp. 520-525. ISSN 1520-6300

Cook, Gillian R., Krithika, S., Edwards, Melissa, Kavanagh, Paula and Parra, Esteban J. (2014) Quantitative measurement of odor detection thresholds using an air dilution olfactometer, and association with genetic variants in a sample of diverse ancestry. PeerJ, 2. e643. ISSN 2167-8359

Mahajan, Anubha, Go, Min Jin, Zhang, Weihua, Below, Jennifer E., Gaulton, Kyle J., Ferreira, Teresa, Horikoshi, Momoko, Johnson, Andrew D., Ng, Maggie C. Y., Prokopenko, Inga, Saleheen, Danish, Wang, Xu, Zeggini, Eleftheria, Abecasis, Goncalo R., Adair, Linda S., Almgren, Peter, Atalay, Mustafa, Aung, Tin, Baldassarre, Damiano, Balkau, Beverley, Bao, Yuqian, Barnett, Anthony H., Barroso, Ines, Basit, Abdul, Been, Latonya F., Beilby, John, Bell, Graeme I., Benediktsson, Rafn, Bergman, Richard N., Boehm, Bernhard O., Boerwinkle, Eric, Bonnycastle, Lori L., Burtt, Noël, Cai, Qiuyin, Campbell, Harry, Carey, Jason, Cauchi, Stephane, Caulfield, Mark, Chan, Juliana C. N., Chang, Li-Ching, Chang, Tien-Jyun, Chang, Yi-Cheng, Charpentier, Guillaume, Chen, Chien-Hsiun, Chen, Han, Chen, Yuan-Tsong, Chia, Kee-Seng, Chidambaram, Manickam, Chines, Peter S, Cho, Nam H, Cho, Young Min, Chuang, Lee-Ming, Collins, Francis S., Cornelis, Marilyn C., Couper, David J., Crenshaw, Andrew T., van Dam, Rob M., Danesh, John, Das, Debashish, de Faire, Ulf, Dedoussis, George, Deloukas, Panos, Dimas, Antigone S., Dina, Christian, Doney, Alex S. F., Donnelly, Peter J., Dorkhan, Mozhgan, van Duijn, Cornelia, Dupuis, Josée, Edkins, Sarah, Elliott, Paul, Emilsson, Valur, Erbel, Raimund, Eriksson, Johan G., Escobedo, Jorge, Esko, Tonu, Eury, Elodie, Florez, Jose C., Fontanillas, Pierre, Forouhi, Nita G., Forsen, Tom, Fox, Caroline, Fraser, Ross M., Frayling, Timothy M., Froguel, Philippe, Frossard, Philippe, Gao, Yutang, Gertow, Karl, Gieger, Christian, Gigante, Bruna, Grallert, Harald, Grant, George B., Groop, Leif C., Groves, Christopher J., Grundberg, Elin, Guiducci, Candace, Hamsten, Anders, Han, Bok-Ghee, Hara, Kazuo, Hassanali, Neelam, Hattersley, Andrew T., Hayward, Caroline, Hedman, Asa K., Herder, Christian, Hofman, Albert, Holmen, Oddgeir L., Hovingh, Kees, Hreidarsson, Astradur B., Hu, Cheng, Hu, Frank B., Hui, Jennie, Humphries, Steve E., Hunt, Sarah E., Hunter, David J., Hveem, Kristian, Hydrie, Zafar I., Ikegami, Hiroshi, Illig, Thomas, Ingelsson, Erik, Islam, Muhammed, Isomaa, Bo, Jackson, Anne U., Jafar, Tazeen, James, Alan, Jia, Weiping, Jöckel, Karl-Heinz, Jonsson, Anna, Jowett, Jeremy B. M., Kadowaki, Takashi, Kang, Hyun Min, Kanoni, Stavroula, Kao, Wen Hong L., Kathiresan, Sekar, Kato, Norihiro, Katulanda, Prasad, Keinanen-Kiukaanniemi, Sirkka M., Kelly, Ann M., Khan, Hassan, Khaw, Kay-Tee, Khor, Chiea-Chuen, Kim, Hyung-Lae, Kim, Sangsoo, Kim, Young Jin, Kinnunen, Leena, Klopp, Norman, Kong, Augustine, Korpi-Hyövälti, Eeva, Kowlessur, Sudhir, Kraft, Peter, Kravic, Jasmina, Kristensen, Malene M., Krithika, S., Kumar, Ashish, Kumate, Jesus, Kuusisto, Johanna, Kwak, Soo Heon, Laakso, Markku, Lagou, Vasiliki, Lakka, Timo A, Langenberg, Claudia, Langford, Cordelia, Lawrence, Robert, Leander, Karin, Lee, Jen-Mai, Lee, Nanette R., Li, Man, Li, Xinzhong, Li, Yun, Liang, Junbin, Liju, Samuel, Lim, Wei-Yen, Lind, Lars, Lindgren, Cecilia M., Lindholm, Eero, Liu, Ching-Ti, Liu, Jian Jun, Lobbens, Stéphane, Long, Jirong, Loos, Ruth J. F., Lu, Wei, Luan, Jian'an, Lyssenko, Valeriya, Ma, Ronald C. W., Maeda, Shiro, Mägi, Reedik, Männistö, Satu, Matthews, David R., Meigs, James B., Melander, Olle, Metspalu, Andres, Meyer, Julia, Mirza, Ghazala, Mihailov, Evelin, Moebus, Susanne, Mohan, Viswanathan, Mohlke, Karen L., Morris, Andrew D., Mühleisen, Thomas W., Müller-Nurasyid, Martina, Musk, Bill, Nakamura, Jiro, Nakashima, Eitaro, Navarro, Pau, Ng, Peng-Keat, Nica, Alexandra C., Nilsson, Peter M., Njølstad, Inger, Nöthen, Markus M., Ohnaka, Keizo, Ong, Twee Hee, Owen, Katharine R., Palmer, Colin N. A., Pankow, James S., Park, Kyong Soo, Parkin, Melissa, Pechlivanis, Sonali, Pedersen, Nancy L., Peltonen, Leena, Perry, John R. B., Peters, Annette, Pinidiyapathirage, Janani M., Platou, Carl G. P., Potter, Simon, Price, Jackie F., Qi, Lu, Radha, Venkatesan, Rallidis, Loukianos, Rasheed, Asif, Rathmann, Wolfgang, Rauramaa, Rainer, Raychaudhuri, Soumya, Rayner, N. William, Rees, Simon D., Rehnberg, Emil, Ripatti, Samuli, Robertson, Neil, Roden, Michael, Rossin, Elizabeth J., Rudan, Igor, Rybin, Denis, Saaristo, Timo E., Salomaa, Veikko, Saltevo, Juha, Samuel, Maria, Sanghera, Dharambir K., Saramies, Jouko, Scott, James, Scott, Laura J., Scott, Robert A., Segrè, Ayellet V., Sehmi, Joban, Sennblad, Bengt, Shah, Nabi, Shah, Sonia, Shera, A. Samad, Shu, Xiao Ou, Shuldiner, Alan R., Sigurðsson, Gunnar, Sijbrands, Eric, Silveira, Angela, Sim, Xueling, Sivapalaratnam, Suthesh, Small, Kerrin S., So, Wing Yee, Stančáková, Alena, Stefansson, Kari, Steinbach, Gerald, Steinthorsdottir, Valgerdur, Stirrups, Kathleen, Strawbridge, Rona J., Stringham, Heather M., Sun, Qi, Suo, Chen, Syvänen, Ann-Christine, Takayanagi, Ryoichi, Takeuchi, Fumihiko, Tay, Wan Ting, Teslovich, Tanya M., Thorand, Barbara, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Tikkanen, Emmi, Trakalo, Joseph, Tremoli, Elena, Trip, Mieke D., Tsai, Fuu Jen, Tuomi, Tiinamaija, Tuomilehto, Jaakko, Uitterlinden, Andre G., Valladares-Salgado, Adan, Vedantam, Sailaja, Veglia, Fabrizio, Voight, Benjamin F., Wang, Congrong, Wareham, Nicholas J., Wennauer, Roman, Wickremasinghe, Ananda R., Wilsgaard, Tom, Wilson, James F., Wiltshire, Steven, Winckler, Wendy, Wong, Tien Yin, Wood, Andrew R., Wu, Jer-Yuarn, Wu, Ying, Yamamoto, Ken, Yamauchi, Toshimasa, Yang, Mingyu, Yengo, Loic, Yokota, Mitsuhiro, Young, Robin, Zabaneh, Delilah, Zhang, Fan, Zhang, Rong, Zheng, Wei, Zimmet, Paul Z., Altshuler, David, Bowden, Donald W., Cho, Yoon Shin, Cox, Nancy J., Cruz, Miguel, Hanis, Craig L., Kooner, Jaspal, Lee, Jong-Young, Seielstad, Mark, Teo, Yik Ying, Boehnke, Michael, Parra, Esteban J., Chambers, John C, Tai, E. Shyong, McCarthy, Mark I. and Morris, Andrew P. (2014) Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics, 46 (3). pp. 234-244. ISSN 1546-1718