Development and validation of bioelectrical impedance analysis equations for predicting total body water and fat-free mass in North-African adults von Aglago, K E, Menchawy, I El, Kari, K El, Hamdouchi, A El, Barkat, A, Bengueddour, R, Haloui, N El, Mokhtar, N, Aguenaou, H

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Single-nucleotide polymorphism rs1761667 in the CD36 gene is associated with orosensory perception of a fatty acid in obese and normal-weight Moroccan subjects von Bajit, Habiba, Ait Si Mohammed, O., Guennoun, Y., Benaich, S., Bouaiti, E., Belghiti, H., Mrabet, M., Elfahime, E. M., El Haloui, N. E., Saeid, N., El Kari, K., Hichami, A., Khan, N. A., Benkirane, H., Aguenaou, H.

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Impact of flour fortification with elemental iron on the prevalence of anaemia among preschool children in Morocco von El Hamdouchi, A, El Kari, K, Rjimati, L, El Haloui, N, El Mzibri, M, Aguenaou, H, Mokhtar, N

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Development and validation of impedance-based equations for the prediction of total body water and fat free mass in children aged 8 to 11 years von Ben Jemaa, H., mankaï, A., khlifi, S., El Kari, K., Aouidet, A.

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Impact of flour fortification with elemental iron on the prevalence of anaemia among preschool children in Morocco/Impact de l'enrichissement de la farine en fer elementaire sur la... von Hamdouchi, A. El, Kari, K. El, Rjimati, L, Haloui, N. El, Mzibri, M. El, Aguenaou, H, Mokhtar, N

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Impact de l'enrichissement de la farine en fer élémentaire sur la prévalence de l'anémie chez les enfants en âge préscolaire au Maroc/Impact of flour fortification with elemental i... von El Hamdouchi, A, El Kari, K, Rjimati, L, El Haloui, N, El Mzibri, M, Aguenaou, H, Mokhtar, N

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P046 Mesure de la composition corporelle chez les personnes âgées marocaines par les méthodes des isotopes stables et d’impédancemétrie von Bour, A., Hsaini, H. El, Kari, K. El, Janah, K., Belghiti, H., Cha-hid, N., Atef, E., Landais, E., Choua, G., Gartner, A., Aguenaou, H., Mokhtar, N.

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The viral protein corona directs viral pathogenesis and amyloid aggregation von Ezzat, Kariem, Pernemalm, Maria, Pålsson, Sandra, Roberts, Thomas C., Järver, Peter, Dondalska, Aleksandra, Bestas, Burcu, Sobkowiak, Michal J., Levänen, Bettina, Sköld, Magnus, Thompson, Elizabeth A., Saher, Osama, Kari, Otto K., Lajunen, Tatu, Sverremark Ekström, Eva, Nilsson, Caroline, Ishchenko, Yevheniia, Malm, Tarja, Wood, Matthew J. A., Power, Ultan F., Masich, Sergej, Lindén, Anders, Sandberg, Johan K., Lehtiö, Janne, Spetz, Anna-Lena, EL Andaloussi, Samir

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Epithelial-to-mesenchymal transition is not required for lung metastasis but contributes to chemoresistance von Fischer, Kari R., Durrans, Anna, Lee, Sharrell, Sheng, Jianting, Li, Fuhai, Wong, Stephen T. C., Choi, Hyejin, El Rayes, Tina, Ryu, Seongho, Troeger, Juliane, Schwabe, Robert F., Vahdat, Linda T., Altorki, Nasser K., Mittal, Vivek, Gao, Dingcheng

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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome von Sadowski, Carolin E, Lovric, Svjetlana, Ashraf, Shazia, Pabst, Werner L, Gee, Heon Yung, Kohl, Stefan, Engelmann, Susanne, Vega-Warner, Virginia, Fang, Humphrey, Halbritter, Jan, Somers, Michael J, Tan, Weizhen, Shril, Shirlee, Fessi, Inès, Lifton, Richard P, Bockenhauer, Detlef, El-Desoky, Sherif, Kari, Jameela A, Zenker, Martin, Kemper, Markus J, Mueller, Dominik, Fathy, Hanan M, Soliman, Neveen A, Hildebrandt, Friedhelm

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Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis von Daga, Ankana, Majmundar, Amar J., Braun, Daniela A., Gee, Heon Yung, Lawson, Jennifer A., Shril, Shirlee, Jobst-Schwan, Tilman, Vivante, Asaf, Schapiro, David, Tan, Weizhen, Warejko, Jillian K., Widmeier, Eugen, Nelson, Caleb P., Fathy, Hanan M., Gucev, Zoran, Soliman, Neveen A., Hashmi, Seema, Halbritter, Jan, Halty, Margarita, Kari, Jameela A., El-Desoky, Sherif, Ferguson, Michael A., Somers, Michael J.G., Traum, Avram Z., Stein, Deborah R., Daouk, Ghaleb H., Rodig, Nancy M., Katz, Avi, Hanna, Christian, Schwaderer, Andrew L., Sayer, John A., Wassner, Ari J., Mane, Shrikant, Lifton, Richard P., Milosevic, Danko, Tasic, Velibor, Baum, Michelle A., Hildebrandt, Friedhelm

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Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition von Small, Kerrin S., Todorčević, Marijana, Civelek, Mete, El-Sayed Moustafa, Julia S., Wang, Xiao, Simon, Michelle M., Fernandez-Tajes, Juan, Mahajan, Anubha, Horikoshi, Momoko, Hugill, Alison, Glastonbury, Craig A., Quaye, Lydia, Neville, Matt J., Sethi, Siddharth, Yon, Marianne, Pan, Calvin, Che, Nam, Viñuela, Ana, Tsai, Pei-Chien, Nag, Abhishek, Buil, Alfonso, Thorleifsson, Gudmar, Raghavan, Avanthi, Ding, Qiurong, Morris, Andrew P., Bell, Jordana T., Thorsteinsdottir, Unnur, Stefansson, Kari, Laakso, Markku, Dahlman, Ingrid, Arner, Peter, Gloyn, Anna L., Musunuru, Kiran, Lusis, Aldons J., Cox, Roger D., Karpe, Fredrik, McCarthy, Mark I.

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Large-scale integration of the plasma proteome with genetics and disease von Ferkingstad, Egil, Sulem, Patrick, Atlason, Bjarni A., Sveinbjornsson, Gardar, Magnusson, Magnus I., Styrmisdottir, Edda L., Gunnarsdottir, Kristbjorg, Helgason, Agnar, Oddsson, Asmundur, Halldorsson, Bjarni V., Jensson, Brynjar O., Zink, Florian, Halldorsson, Gisli H., Masson, Gisli, Arnadottir, Gudny A., Katrinardottir, Hildigunnur, Juliusson, Kristinn, Magnusson, Magnus K., Magnusson, Olafur Th, Fridriksdottir, Run, Saevarsdottir, Saedis, Gudjonsson, Sigurjon A., Stacey, Simon N., Rognvaldsson, Solvi, Eiriksdottir, Thjodbjorg, Olafsdottir, Thorunn A., Steinthorsdottir, Valgerdur, Tragante, Vinicius, Ulfarsson, Magnus O., Stefansson, Hreinn, Jonsdottir, Ingileif, Holm, Hilma, Rafnar, Thorunn, Melsted, Pall, Saemundsdottir, Jona, Norddahl, Gudmundur L., Lund, Sigrun H., Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Stefansson, Kari

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Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment von Ashraf, Shazia, Kudo, Hiroki, Rao, Jia, Kikuchi, Atsuo, Widmeier, Eugen, Lawson, Jennifer A., Tan, Weizhen, Hermle, Tobias, Warejko, Jillian K., Shril, Shirlee, Airik, Merlin, Jobst-Schwan, Tilman, Lovric, Svjetlana, Braun, Daniela A., Gee, Heon Yung, Schapiro, David, Majmundar, Amar J., Sadowski, Carolin E., Pabst, Werner L., Daga, Ankana, van der Ven, Amelie T., Schmidt, Johanna M., Low, Boon Chuan, Gupta, Anjali Bansal, Tripathi, Brajendra K., Wong, Jenny, Campbell, Kirk, Metcalfe, Kay, Schanze, Denny, Niihori, Tetsuya, Kaito, Hiroshi, Nozu, Kandai, Tsukaguchi, Hiroyasu, Tanaka, Ryojiro, Hamahira, Kiyoshi, Kobayashi, Yasuko, Takizawa, Takumi, Funayama, Ryo, Nakayama, Keiko, Aoki, Yoko, Kumagai, Naonori, Iijima, Kazumoto, Fehrenbach, Henry, Kari, Jameela A., El Desoky, Sherif, Jalalah, Sawsan, Bogdanovic, Radovan, Stajić, Nataša, Zappel, Hildegard, Rakhmetova, Assel, Wassmer, Sharon-Rose, Jungraithmayr, Therese, Strehlau, Juergen, Kumar, Aravind Selvin, Bagga, Arvind, Soliman, Neveen A., Mane, Shrikant M., Kaufman, Lewis, Lowy, Douglas R., Jairajpuri, Mohamad A., Lifton, Richard P., Pei, York, Zenker, Martin, Kure, Shigeo, Hildebrandt, Friedhelm

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Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract von van der Ven, Amelie T, Connaughton, Dervla M, Ityel, Hadas, Mann, Nina, Nakayama, Makiko, Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Schulz, Julian, Braun, Daniela A, Schmidt, Johanna Magdalena, Schapiro, David, Schneider, Ronen, Warejko, Jillian K, Daga, Ankana, Majmundar, Amar J, Tan, Weizhen, Jobst-Schwan, Tilman, Hermle, Tobias, Widmeier, Eugen, Ashraf, Shazia, Amar, Ali, Hoogstraaten, Charlotte A, Hugo, Hannah, Kitzler, Thomas M, Kause, Franziska, Kolvenbach, Caroline M, Dai, Rufeng, Spaneas, Leslie, Amann, Kassaundra, Stein, Deborah R, Baum, Michelle A, Somers, Michael J G, Rodig, Nancy M, Ferguson, Michael A, Traum, Avram Z, Daouk, Ghaleb H, Bogdanović, Radovan, Stajić, Natasa, Soliman, Neveen A, Kari, Jameela A, El Desoky, Sherif, Fathy, Hanan M, Milosevic, Danko, Al-Saffar, Muna, Awad, Hazem S, Eid, Loai A, Selvin, Aravind, Senguttuvan, Prabha, Sanna-Cherchi, Simone, Rehm, Heidi L, MacArthur, Daniel G, Lek, Monkol, Laricchia, Kristen M, Wilson, Michael W, Mane, Shrikant M, Lifton, Richard P, Lee, Richard S, Bauer, Stuart B, Lu, Weining, Reutter, Heiko M, Tasic, Velibor, Shril, Shirlee, Hildebrandt, Friedhelm

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Outcomes after thrombus aspiration for ST elevation myocardial infarction: 1-year follow-up of the prospective randomised TOTAL trial von Jolly, Sanjit S, Dr, Cairns, John A, Prof, Yusuf, Salim, Prof, Rokoss, Michael J, MD, Gao, Peggy, MSc, Meeks, Brandi, MEng, Kedev, Sasko, Prof, Stankovic, Goran, MD, Moreno, Raul, MD, Gershlick, Anthony, Prof, Chowdhary, Saqib, MD, Lavi, Shahar, MD, Niemela, Kari, MD, Bernat, Ivo, MD, Cantor, Warren J, MD, Cheema, Asim N, MD, Steg, Philippe Gabriel, Prof, Welsh, Robert C, Prof, Sheth, Tej, MD, Bertrand, Olivier F, MD, Avezum, Alvaro, Prof, Bhindi, Ravinay, MBBS, Natarajan, Madhu K, Prof, Horak, David, MD, Leung, Raymond C M, MD, Kassam, Saleem, MD, Rao, Sunil V, MD, El-Omar, Magdi, MD, Mehta, Shamir R, Prof, Velianou, James L, MD, Pancholy, Samir, MD, Džavík, Vladimír, Prof

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Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome von Braun, Daniela A, Warejko, Jillian K, Ashraf, Shazia, Tan, Weizhen, Daga, Ankana, Schneider, Ronen, Hermle, Tobias, Jobst-Schwan, Tilman, Widmeier, Eugen, Majmundar, Amar J, Nakayama, Makiko, Schapiro, David, Rao, Jia, Schmidt, Johanna Magdalena, Hoogstraten, Charlotte A, Hugo, Hannah, Bakkaloglu, Sevcan A, Kari, Jameela A, El Desoky, Sherif, Daouk, Ghaleb, Mane, Shrikant, Lifton, Richard P, Shril, Shirlee, Hildebrandt, Friedhelm

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program von Taliun, Daniel, Kessler, Michael D., Carlson, Jedidiah, Taliun, Sarah A. Gagliano, Kang, Hyun Min, Pitsillides, Achilleas N., Emde, Anne-Katrin, Clarke, Wayne E., Shetty, Amol C., Wong, Quenna, Bobo, Dean M., Aguet, François, Albert, Christine, Aslibekyan, Stella, Barnard, John, Barr, R. Graham, Barwick, Lucas, Becker, Lewis C., Bielak, Lawrence F., Blangero, John, Bowden, Donald W., Burchard, Esteban G., Chalazan, Brandon, Chasman, Daniel I., Chen, Yii-Der Ida, Choi, Seung Hoan, Chung, Mina K., Curran, Joanne E., Daya, Michelle, Ellinor, Patrick T., Fatkin, Diane, Fingerlin, Tasha, Forer, Lukas, Franceschini, Nora, Germer, Soren, Gladwin, Mark T., Hall, Michael E., He, Jiang, Johnsen, Jill M., Johnson, Andrew D., Kardia, Sharon L. R., Klemmer, Robert, Kooperberg, Charles, Köttgen, Anna, Lange, Leslie A., Lin, Xihong, Lin, Keng-Han, Liu, Chunyu, Loos, Ruth J. F., Gerszten, Robert, Lunetta, Kathryn L., Mak, Angel C. Y., Manichaikul, Ani, Manning, Alisa K., Mathias, Rasika A., McManus, David D., McGarvey, Stephen T., Meigs, James B., Minear, Mollie A., Mitchell, Braxton D., Mohanty, Sanghamitra, Montasser, May E., Montgomery, Courtney, Morrison, Alanna C., Murabito, Joanne M., Natale, Andrea, Nelson, Sarah C., Palmer, Nicholette D., Pankratz, Nathan, Peyser, Patricia A., Post, Wendy S., Psaty, Bruce M., Rao, D. C., Reiner, Alexander P., Roden, Dan, Rotter, Jerome I., Schoenherr, Sebastian, Seo, Jeong-Sun, Sheu, Wayne H., Smith, Nicholas L., Smith, Jennifer A., Stilp, Adrienne M., Telen, Marilyn, Thornton, Timothy A., Tracy, Russell P., Van Den Berg, David J., Vasan, Ramachandran S., Vrieze, Scott, Weng, Lu-Chen, Zhao, Xutong, Boerwinkle, Eric, Gibbs, Richard, Rich, Stephen S., Silverman, Edwin K., Qasba, Pankaj, Gan, Weiniu, Zöllner, Sebastian, Wilson, James G., Laurie, Cathy C., Jaquish, Cashell E.

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Stillbirths: rates, risk factors, and acceleration towards 2030 von Lawn, Joy E, Prof, Blencowe, Hannah, MRCPCH, Waiswa, Peter, PhD, Amouzou, Agbessi, PhD, Mathers, Colin, PhD, Hogan, Dan, PhD, Flenady, Vicki, PhD, Frøen, J Frederik, PhD, Qureshi, Zeshan U, BM, Calderwood, Claire, BM, Shiekh, Suhail, MSc, Jassir, Fiorella Bianchi, MSc, You, Danzhen, PhD, McClure, Elizabeth M, PhD, Mathai, Matthews, PhD, Cousens, Simon, Prof

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Identification of Reprogrammed Myeloid Cell Transcriptomes in NSCLC von Durrans, Anna, Gao, Dingcheng, Gupta, Ravi, Fischer, Kari R, Choi, Hyejin, El Rayes, Tina, Ryu, Seongho, Nasar, Abu, Spinelli, Cathy F, Andrews, Weston, Elemento, Olivier, Nolan, Daniel, Stiles, Brendon, Rafii, Shahin, Narula, Navneet, Davuluri, Ramana, Altorki, Nasser K, Mittal, Vivek

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