Preclinical Aortic Atherosclerosis in Adolescents With Chronic Disease von Ververs, Francesca A, Eikendal, Anouk L M, Kofink, Daniel, Nuboer, Roos, Westenberg, Jos J M, Hovenkamp, Gijs T, Kemps, Jitske J A, Coenen, Iris C J, Daems, Joëlle J N, Claus, Laura R, Ju, Yillie, Wulffraat, Nico M, van der Ent, Cornelis K, Monaco, Claudia, Boes, Marianne, Leiner, Tim, Grotenhuis, Heynric B, Schipper, Henk S

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KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease von Boulogne, Floranne, Claus, Laura R, Wiersma, Henry, Oelen, Roy, Schukking, Floor, de Klein, Niek, Li, Shuang, Westra, Harm-Jan, van der Zwaag, Bert, van Reekum, Franka, Sierks, Dana, Schönauer, Ria, Li, Zhigui, Bijlsma, Emilia K, Bos, Willem Jan W, Halbritter, Jan, Knoers, Nine V A M, Besse, Whitney, Deelen, Patrick, Franke, Lude, van Eerde, Albertien M

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Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract von Münch, Johannes, Engesser, Marie, Schönauer, Ria, Hamm, J. Austin, Hartig, Christin, Hantmann, Elena, Akay, Gulsen, Pehlivan, Davut, Mitani, Tadahiro, Coban Akdemir, Zeynep, Tüysüz, Beyhan, Shirakawa, Toshihiko, Dateki, Sumito, Claus, Laura R., van Eerde, Albertien M., Smol, Thomas, Devisme, Louise, Franquet, Hélène, Attié-Bitach, Tania, Wagner, Timo, Bergmann, Carsten, Höhn, Anne Kathrin, Shril, Shirlee, Pollack, Ari, Wenger, Tara, Scott, Abbey A., Paolucci, Sarah, Buchan, Jillian, Gabriel, George C., Posey, Jennifer E., Lupski, James R., Petit, Florence, McCarthy, Andrew A., Pazour, Gregory J., Lo, Cecilia W., Popp, Bernt, Halbritter, Jan

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The Importance of Copy Number Variant Analysis in Patients with Monogenic Kidney Disease von Claus, Laura R., Ernst, Robert F., Elferink, Martin G., van Deutekom, Hanneke W.M., van der Zwaag, Bert, van Eerde, Albertien M.

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Review of genetic testing in kidney disease patients: Diagnostic yield of single nucleotide variants and copy number variations evaluated across and within kidney phenotype groups von Claus, Laura R, Snoek, Rozemarijn, Knoers, Nine V A M, van Eerde, Albertien M

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Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease von Claus, Laura R., Chen, Chuan, Stallworth, Jennifer, Turner, Joshua L., Slaats, Gisela G., Mabillard, Holly, Senum, Sarah R., Srikanth, Sujata, Flanagan-Steet, Heather, Louie, Raymond J., Silver, Josh, Lerner-Ellis, Jordan, Morel, Chantal, Mighton, Chloe, Sleutels, Frank, van Slegtenhorst, Marjon, van Ham, Tjakko, Brooks, Alice S., Dorresteijn, Eiske M., Barakat, Tahsin Stefan, Dahan, Karin, Demoulin, Nathalie, Goffin, Eric Jean, Olinger, Eric, Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Elgar, Greg, Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jackson, Rob, Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., Maleady-Crowe, Fiona, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Need, Anna C., O’Donovan, Peter, Odhams, Chris A., Patch, Christine, Pereira, Mariana Buongermino, Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Rendon, Augusto, Rogers, Tim, Savage, Kevin, Sawant, Kushmita, Scott, Richard H., Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Thompson, Simon R., Tucci, Arianna, Welland, Matthew J., Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M., Larsen, Martin, Hertz, Jens Michael, Lilien, Marc R., Obeidová, Lena, Stone, Hillarey K., Kerecuk, Larissa, Gurgu, Mihai, Yousef Yengej, Fjodor A., Ammerlaan, Carola M.E., Rookmaaker, Maarten B., Hanna, Christian, Rogers, R. Curtis, Duran, Karen, Peters, Edith, Sayer, John A., van Haaften, Gijs, Harris, Peter C., Ling, Kun, Mason, Jennifer M., van Eerde, Albertien M., Steet, Richard

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KidneyNetwork Uses Kidney-Derived Gene Expression Data to Predict and Prioritize Novel Genes Involved in Kidney Disease: PO1200 von Claus, Laura R., Boulogne, Floranne, Wiersma, Henry, Oelen, Roy, Schukking, Floor, de Klein, Niek, Li, Shuang, Westra, Harm-Jan, Van der zwaag, Bert, Sierks, Dana, Schönauer, Ria, Halbritter, Jan, Knoers, Nine V., Deelen, Patrick, Franke, Lude, van Eerde, Albertien M.

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Heterozygous Variants in NEK8 Kinase Domain Cause an Autosomal-Dominant Ciliopathy: PO1246 von Claus, Laura R., Stallworth, Jennifer, van Jaarsveld, Richard H., Louie, Raymond, Silver, Josh, Lerner-Ellis, Jordan, Morel, Chantal F., Mighton, Chloe, Ziegler, Alban, Barakat, Tahsin Stefan, Dahan, Karin, Demoulin, Nathalie, Goffin, Eric, Larsen, Martin J., Hertz, Jens Michael, Lilien, Marc, Olinger, Eric G., Sayer, John A., Obeidova, Lena, Seeman, Tomas, Rogers, Richard C., Duran, Karen J., van Haaften, Gijs W., Steet, Richard, van Eerde, Albertien M.

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The Importance of Copy Number Variant Analysis in Patients with Monogenic Kidney Disease von Claus, Laura R, Ernst, Robert F, Elferink, Martin G, van Deutekom, Hanneke W.M, van der Zwaag, Bert, van Eerde, Albertien M

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GeNepher data- and biobank for patients with (suspected) genetic kidney disease: Rationale, design and status update von Claus, Laura R, Lekkerkerker, Iris, van der Zwaag, Bert, Nguyen, Tri Q, Knoers, Nine V.A.M, de Borst, Martin H, Rookmaker, Maarten B, Lilien, Marc R, van Eerde, Albertien M

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GeNepher data- and biobank for patients with (suspected) genetic kidney disease: Rationale, design and status update von Claus, Laura R., Lekkerkerker, Iris, van der Zwaag, Bert, Nguyen, Tri Q., Knoers, Nine V.A.M., de Borst, Martin H., Rookmaker, Maarten B., Lilien, Marc R., van Eerde, Albertien M.

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Preclinical Aortic Atherosclerosis in Adolescents With Chronic Disease von Ververs, Francesca A, Eikendal, Anouk L M, Kofink, Daniel, Nuboer, Roos, Westenberg, Jos J M, Hovenkamp, Gijs T, Kemps, Jitske J A, Coenen, Iris C J, Daems, Joëlle J N, Claus, Laura R, Ju, Yillie, Wulffraat, Nico M, van der Ent, Cornelis K, Monaco, Claudia, Boes, Marianne, Leiner, Tim, Grotenhuis, Heynric B, Schipper, Henk S

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Solutes unmask differences in clustering versus phase separation of FET proteins von Kar, Mrityunjoy, Vogel, Laura T., Chauhan, Gaurav, Felekyan, Suren, Ausserwöger, Hannes, Welsh, Timothy J., Dar, Furqan, Kamath, Anjana R., Knowles, Tuomas P. J., Hyman, Anthony A., Seidel, Claus A. M., Pappu, Rohit V.

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Chromosome errors in human eggs shape natural fertility over reproductive life span von Gruhn, Jennifer R, Zielinska, Agata P, Shukla, Vallari, Blanshard, Robert, Capalbo, Antonio, Cimadomo, Danilo, Nikiforov, Dmitry, Chan, Andrew Chi-Ho, Newnham, Louise J, Vogel, Ivan, Scarica, Catello, Krapchev, Marta, Taylor, Deborah, Kristensen, Stine Gry, Cheng, Junping, Ernst, Erik, Bjørn, Anne-Mette Bay, Colmorn, Lotte Berdiin, Blayney, Martyn, Elder, Kay, Liss, Joanna, Hartshorne, Geraldine, Grøndahl, Marie Louise, Rienzi, Laura, Ubaldi, Filippo, McCoy, Rajiv, Lukaszuk, Krzysztof, Andersen, Claus Yding, Schuh, Melina, Hoffmann, Eva R

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West Nile virus experimental evolution in vivo and the trade-off hypothesis von Deardorff, Eleanor R, Fitzpatrick, Kelly A, Jerzak, Greta V S, Shi, Pei-Yong, Kramer, Laura D, Ebel, Gregory D

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Hierarchically related lineage-restricted fates of multipotent haematopoietic stem cells von Carrelha, Joana, Meng, Yiran, Kettyle, Laura M., Luis, Tiago C., Norfo, Ruggiero, Alcolea, Verónica, Boukarabila, Hanane, Grasso, Francesca, Gambardella, Adriana, Grover, Amit, Högstrand, Kari, Lord, Allegra M., Sanjuan-Pla, Alejandra, Woll, Petter S., Nerlov, Claus, Jacobsen, Sten Eirik W.

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Early Last Interglacial ocean warming drove substantial ice mass loss from Antarctica von Turney, Chris S. M., Fogwill, Christopher J., Golledge, Nicholas R., McKay, Nicholas P., van Sebille, Erik, Jones, Richard T., Etheridge, David, Rubino, Mauro, Thornton, David P., Davies, Siwan M., Ramsey, Christopher Bronk, Thomas, Zoe A., Bird, Michael I., Munksgaard, Niels C., Kohno, Mika, Woodward, John, Winter, Kate, Weyrich, Laura S., Rootes, Camilla M., Millman, Helen, Albert, Paul G., Rivera, Andres, van Ommen, Tas, Curran, Mark, Moy, Andrew, Rahmstorf, Stefan, Kawamura, Kenji, Hillenbrand, Claus-Dieter, Weber, Michael E., Manning, Christina J., Young, Jennifer, Cooper, Alan

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Serum neurofilament light chain - A potential biomarker for polyneuropathy in type 2 diabetes? von Määttä, Laura L, Andersen, Signe T, Parkner, Tina, Hviid, Claus V B, Bjerg, Lasse, Kural, Mustafa A, Charles, Morten, Søndergaard, Esben, Sandbæk, Annelli, Tankisi, Hatice, Witte, Daniel R, Jensen, Troels S

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Metabolic profiling detects early effects of environmental and lifestyle exposure to cadmium in a human population von Ellis, James K, Athersuch, Toby J, Thomas, Laura D K, Teichert, Friederike, Pérez-Trujillo, Miriam, Svendsen, Claus, Spurgeon, David J, Singh, Rajinder, Järup, Lars, Bundy, Jacob G, Keun, Hector C

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IKZF1 plus Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia von Stanulla, Martin, Dagdan, Elif, Zaliova, Marketa, Möricke, Anja, Palmi, Chiara, Cazzaniga, Giovanni, Eckert, Cornelia, Te Kronnie, Geertruy, Bourquin, Jean-Pierre, Bornhauser, Beat, Koehler, Rolf, Bartram, Claus R, Ludwig, Wolf-Dieter, Bleckmann, Kirsten, Groeneveld-Krentz, Stefanie, Schewe, Denis, Junk, Stefanie V, Hinze, Laura, Klein, Norman, Kratz, Christian P, Biondi, Andrea, Borkhardt, Arndt, Kulozik, Andreas, Muckenthaler, Martina U, Basso, Giuseppe, Valsecchi, Maria Grazia, Izraeli, Shai, Petersen, Britt-Sabina, Franke, Andre, Dörge, Petra, Steinemann, Doris, Haas, Oskar A, Panzer-Grümayer, Renate, Cavé, Hélène, Houlston, Richard S, Cario, Gunnar, Schrappe, Martin, Zimmermann, Martin

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