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

Volltext

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.

Volltext

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

Volltext

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.

Volltext

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

Volltext

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

Volltext

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.

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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.

Volltext

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

Volltext

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

Volltext

GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome von Hermle, Tobias, Schneider, Ronen, Schapiro, David, Braun, Daniela A, van der Ven, Amelie T, Warejko, Jillian K, Daga, Ankana, Widmeier, Eugen, Nakayama, Makiko, Jobst-Schwan, Tilman, Majmundar, Amar J, Ashraf, Shazia, Rao, Jia, Finn, Laura S, Tasic, Velibor, Hernandez, Joel D, Bagga, Arvind, Jalalah, Sawsan M, El Desoky, Sherif, Kari, Jameela A, Laricchia, Kristen M, Lek, Monkol, Rehm, Heidi L, MacArthur, Daniel G, Mane, Shrikant, Lifton, Richard P, Shril, Shirlee, Hildebrandt, Friedhelm

Volltext