Items where Author is "Krithika, S."

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Zagaglia, Sara and Steel, Dora and Krithika, S. and Hernandez-Hernandez, Laura and Custodio, Helena M. and Gorman, Kathleen M. and Vezyroglou, Aikaterini and Møller, Rikke S. and King, Mary D. and Hammer, Trine B. and Spaull, Robert and Fazeli, Walid and Bartolomaeus, Tobias and Doummar, Diane and Keren, Boris and Mignot, Cyril and Bednarek, Nathalie and Cross, J. Helen and Mallick, Andrew A. and Sanchis-Juan, Alba and Basu, Anna and Raymond, F. Lucy and Lynch, Bryan J. and Majumdar, Anirban and Stamberger, Hannah and Weckhuysen, Sarah and 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 and Hernandez-Hernandez, Laura and Balestrini, Simona and Krithika, S. and Moran, Nicholas and Hale, Blake and 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. and Gardella, Elena and Encinas, Alejandra C. and Lehesjoki, Anna‐Elina and Linnankivi, Tarja and Petersen, Michael B. and Lund, Ida C. B. and Blichfeldt, Susanne and Miranda, Maria J. and Pal, Deb K. and Lascelles, Karine and Procopis, Peter and Orsini, Alessandro and Bonuccelli, Alice and Giacomini, Thea and Helbig, Ingo and Fenger, Christina D. and Sisodiya, Sanjay M. and Hernandez‐Hernandez, Laura and Krithika, S. and Rumple, Melissa and Masnada, Silvia and Valente, Marialuisa and Cereda, Cristina and Giordano, Lucio and Accorsi, Patrizia and Bürki, Sarah E. and Mancardi, Margherita and Korff, Christian and Guerrini, Renzo and Spiczak, Sarah and Hoffman‐Zacharska, Dorota and Mazurczak, Tomasz and Coppola, Antonietta and Buono, Salvatore and Vecchi, Marilena and Hammer, Michael F. and Varesio, Costanza and Veggiotti, Pierangelo and Lal, Dennis and Brünger, Tobias and Zara, Federico and Striano, Pasquale and 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 and Picard, Fabienne and Verbeek, Nienke E. and van Kempen, Marjan and Brilstra, Eva H. and Lesca, Gaetan and Conti, Valerio and Guerrini, Renzo and Bisulli, Francesca and Licchetta, Laura and Pippucci, Tommaso and Tinuper, Paolo and Hirsch, Edouard and de Saint Martin, Anne and Chelly, Jamel and Rudolf, Gabrielle and Chipaux, Mathilde and Ferrand-Sorbets, Sarah and Dorfmüller, Georg and Sisodiya, Sanjay and Balestrini, Simona and Schoeler, Natasha and Hernandez-Hernandez, Laura and Krithika, S. and Oegema, Renske and Hagebeuk, Eveline and Gunning, Boudewijn and Deckers, Charles and Berghuis, Bianca and Wegner, Ilse and Niks, Erik and Jansen, Floor E. and Braun, Kees and de Jong, Daniëlle and Rubboli, Guido and Talvik, Inga and Sander, Valentin and Uldall, Peter and Jacquemont, Marie-Line and Nava, Caroline and Leguern, Eric and Julia, Sophie and Gambardella, Antonio and d’Orsi, Giuseppe and Crichiutti, Giovanni and Faivre, Laurence and Darmency, Veronique and Benova, Barbora and Krsek, Pavel and Biraben, Arnaud and Lebre, Anne-Sophie and Jennesson, Mélanie and Sattar, Shifteh and Marchal, Cécile and Nordli, Douglas R. and Lindstrom, Kristin and Striano, Pasquale and Lomax, Lysa B. and Kiss, Courtney and Bartolomei, Fabrice and Lepine, Anne F. and Schoonjans, An-Sofie and Stouffs, Katrien and Jansen, Anna and Panagiotakaki, Eleni and Ricard-Mousnier, Brigitte and Thevenon, Julien and de Bellescize, Julitta and Catenoix, Hélène and Dorn, Thomas and Zenker, Martin and Müller-Schlüter, Karen and Brandt, Christian and Krey, Ilona and Polster, Tilman and Wolff, Markus and Balci, Meral and Rostasy, Kevin and Achaz, Guillaume and Zacher, Pia and Becher, Thomas and Cloppenborg, Thomas and Yuskaitis, Christopher J. and Weckhuysen, Sarah and Poduri, Annapurna and Lemke, Johannes R. and 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 and Selch, Christina and Nisevic, Jelena R. and Mei, Davide and Michalak, Zuzanna and Hernandez-Hernandez, Laura and Krithika, S. and Vezyroglou, Katharina and Varadkar, Sophia M. and Pepler, Alexander and Biskup, Saskia and Leão, Miguel and Gärtner, Jutta and Merkenschlager, Andreas and Jaksch, Michaela and Møller, Rikke S. and Gardella, Elena and Kristiansen, Britta S. and Hansen, Lars K. and Vari, Maria S. and Helbig, Katherine L. and Desai, Sonal and Smith-Hicks, Constance L. and Hino-Fukuyo, Naomi and Talvik, Tiina and Laugesaar, Rael and Ilves, Pilvi and Õunap, Katrin and Körber, Ingrid and Hartlieb, Till and Kudernatsch, Manfred and Winkler, Peter and Schimmel, Mareike and Hasse, Anette and Knuf, Markus and Heinemeyer, Jan and Makowski, Christine and Ghedia, Sondhya and Subramanian, Gopinath M. and Striano, Pasquale and Thomas, Rhys H. and Micallef, Caroline and Thom, Maria and Werring, David J. and Kluger, Gerhard J. and Cross, J. Helen and Guerrini, Renzo and Balestrini, Simona and Sisodiya, Sanjay M. (2018) Neurologic phenotypes associated with COL4A1/2 mutations. Neurology, 91 (22). e2078-e2088. ISSN 1526-632X

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

This list was generated on Sun Sep 19 02:26:27 2021 BST.