Focal segmental glomerulosclerosis in association with neurofibromatosis type 1: a case report and proposed molecular pathways

por Afshinnia, Farsad, Vega-Warner, Virginia, Killen, Paul
Publicado 2013

Focal segmental glomerulosclerosis in association with neurofibromatosis type 1: a case report and proposed molecular pathways

por Afshinnia, Farsad, Vega-Warner, Virginia, Killen, Paul
Publicado 2013

A Case of Hyperphosphatemia and Elevated Fibroblast Growth Factor 23: A Brief Review of Hyperphosphatemia and Fibroblast Growth Factor 23 Pathway

por Wang, Joseph, Vogt, Beth, Sethi, Sidharth Kumar, Sampson, Matthew G., Vega-Warner, Virginia, Otto, Edgar A., Raina, Rupesh
Publicado 2017

Steroid-resistant nephrotic syndrome: impact of genetic testing

por Kari, Jameela A., El-Desoky, Sherif M., Gari, Mamdooh, Malik, Khalid, Vega-Warner, Virginia, Lovric, Svjetlana, Bockenhauer, Detlef
Publicado 2013

Whole Exome Sequencing Reveals Novel PHEX Splice Site Mutations in Patients with Hypophosphatemic Rickets

por Ma, Sara L., Vega-Warner, Virginia, Gillies, Christopher, Sampson, Matthew G., Kher, Vijay, Sethi, Sidharth K., Otto, Edgar A.
Publicado 2015

Family Risk for Depression and Prioritization of Religion or Spirituality: Early Neurophysiological Modulations of Motivated Attention

por Kayser, Jürgen, Tenke, Craig E., Svob, Connie, Gameroff, Marc J., Miller, Lisa, Skipper, Jamie, Warner, Virginia, Wickramaratne, Priya, Weissman, Myrna M.
Publicado 2019

Novel compound heterozygous mutations in AMN cause Imerslund-Gräsbeck syndrome in two half-sisters: a case report

por Montgomery, Emma, Sayer, John A., Baines, Laura A., Hynes, Ann Marie, Vega-Warner, Virginia, Johnson, Sally, Goodship, Judith A., Otto, Edgar A.
Publicado 2015

Motivated attention and family risk for depression: Neuronal generator patterns at scalp elicited by lateralized aversive pictures reveal blunted emotional responsivity

por Kayser, Jürgen, Tenke, Craig E., Abraham, Karen S., Alschuler, Daniel M., Alvarenga, Jorge E., Skipper, Jamie, Warner, Virginia, Bruder, Gerard E., Weissman, Myrna M.
Publicado 2017

A Familial Infantile Renal Failure

por Sethi, Sidharth K., Wadhwani, Nikita, Jha, Pranaw, Duggal, Rajan, Vega-Warner, Virginia, Raina, Rupesh, Bansal, Shyam B., Kher, Vijay, Sampson, Matthew G., Otto, Edgar A.
Publicado 2016

tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine

por Gillies, Christopher E., Otto, Edgar A., Vega-Warner, Virginia, Robertson, Catherine C., Sanna-Cherchi, Simone, Gharavi, Ali, Crawford, Brendan, Bhimma, Rajendra, Winkler, Cheryl, Kang, Hyun Min, Sampson, Matthew G.
Publicado 2016

NPHS2 V260E Is a Frequent Cause of Steroid-Resistant Nephrotic Syndrome in Black South African Children

por Asharam, Kareshma, Bhimma, Rajendra, David, Victor A., Coovadia, Hoosen M., Qulu, Wenkosi P., Naicker, Thajasvarie, Gillies, Christopher E., Vega-Warner, Virginia, Johnson, Randall C., Limou, Sophie, Kopp, Jeffrey B., Sampson, Mathew, Nelson, George W., Winkler, Cheryl A.
Publicado 2018

A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations

por Hildebrandt, Friedhelm, Heeringa, Saskia F., Rüschendorf, Franz, Attanasio, Massimo, Nürnberg, Gudrun, Becker, Christian, Seelow, Dominik, Huebner, Norbert, Chernin, Gil, Vlangos, Christopher N., Zhou, Weibin, O'Toole, John F., Hoskins, Bethan E., Wolf, Matthias T. F., Hinkes, Bernward G., Chaib, Hassan, Ashraf, Shazia, Schoeb, Dominik S., Ovunc, Bugsu, Allen, Susan J., Vega-Warner, Virginia, Wise, Eric, Harville, Heather M., Lyons, Robert H., Washburn, Joseph, MacDonald, James, Nürnberg, Peter, Otto, Edgar A.
Publicado 2009

Comparing Kidney Health Outcomes in Children, Adolescents, and Adults With Focal Segmental Glomerulosclerosis

por Gipson, Debbie S., Troost, Jonathan P., Spino, Cathie, Attalla, Samara, Tarnoff, Joshua, Massengill, Susan, Lafayette, Richard, Vega-Warner, Virginia, Adler, Sharon, Gipson, Patrick, Elliott, Matthew, Kaskel, Frederick, Fermin, Damian, Moxey-Mims, Marva, Fine, Richard N., Brown, Elizabeth J., Reidy, Kimberly, Tuttle, Katherine, Gibson, Keisha, Lemley, Kevin V., Greenbaum, Larry A., Atkinson, Meredith A., Hingorani, Sangeeta, Srivastava, Tarak, Sethna, Christine B., Meyers, Kevin, Tran, Cheryl, Dell, Katherine M., Wang, Chia-shi, Yee, Jennifer Lai, Sampson, Matthew G., Gbadegesin, Rasheed, Lin, J. J., Brady, Tammy, Rheault, Michelle, Trachtman, Howard
Publicado 2022

An integrated organoid omics map extends modeling potential of kidney disease

por Lassé, Moritz, El Saghir, Jamal, Berthier, Celine C., Eddy, Sean, Fischer, Matthew, Laufer, Sandra D., Kylies, Dominik, Hutzfeldt, Arvid, Bonin, Léna Lydie, Dumoulin, Bernhard, Menon, Rajasree, Vega-Warner, Virginia, Eichinger, Felix, Alakwaa, Fadhl, Fermin, Damian, Billing, Anja M., Minakawa, Akihiro, McCown, Phillip J., Rose, Michael P., Godfrey, Bradley, Meister, Elisabeth, Wiech, Thorsten, Noriega, Mercedes, Chrysopoulou, Maria, Brandts, Paul, Ju, Wenjun, Reinhard, Linda, Hoxha, Elion, Grahammer, Florian, Lindenmeyer, Maja T., Huber, Tobias B., Schlüter, Hartmut, Thiel, Steffen, Mariani, Laura H., Puelles, Victor G., Braun, Fabian, Kretzler, Matthias, Demir, Fatih, Harder, Jennifer L., Rinschen, Markus M.
Publicado 2023

Whole exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies

por Gee, Heon Yung, Otto, Edgar A., Hurd, Toby W., Ashraf, Shazia, Chaki, Moumita, Cluckey, Andrew, Vega-Warner, Virginia, Saisawat, Pawaree, Diaz, Katrina A., Fang, Humphrey, Kohl, Stefan, Allen, Susan J., Airik, Rannar, Zhou, Weibin, Ramaswami, Gokul, Janssen, Sabine, Fu, Clementine, Innis, Jamie L., Weber, Stefanie, Vester, Udo, Davis, Erica E., Katsanis, Nicholas, Fathy, Hanan M., Jeck, Nikola, Klaus, Gunther, Nayir, Ahmet, Rahim, Khawla A., Attrach, Ibrahim Al, Hassoun, Ibrahim Al, Ozturk, Savas, Drozdz, Dorota, Helmchen, Udo, O’Toole, John F., Attanasio, Massimo, Nürnberg, Gudrun, Nürnberg, Peter, Washburn, Joseph, MacDonald, James, James, Jeffrey W., Levy, Shawn, Hildebrandt, Friedhelm
Publicado 2013

FAT1 mutations cause a glomerulotubular nephropathy

por Gee, Heon Yung, Sadowski, Carolin E., Aggarwal, Pardeep K., Porath, Jonathan D., Yakulov, Toma A., Schueler, Markus, Lovric, Svjetlana, Ashraf, Shazia, Braun, Daniela A., Halbritter, Jan, Fang, Humphrey, Airik, Rannar, Vega-Warner, Virginia, Cho, Kyeong Jee, Chan, Timothy A., Morris, Luc G. T., ffrench-Constant, Charles, Allen, Nicholas, McNeill, Helen, Büscher, Rainer, Kyrieleis, Henriette, Wallot, Michael, Gaspert, Ariana, Kistler, Thomas, Milford, David V., Saleem, Moin A., Keng, Wee Teik, Alexander, Stephen I., Valentini, Rudolph P., Licht, Christoph, Teh, Jun C., Bogdanovic, Radovan, Koziell, Ania, Bierzynska, Agnieszka, Soliman, Neveen A., Otto, Edgar A., Lifton, Richard P., Holzman, Lawrence B., Sibinga, Nicholas E. S., Walz, Gerd, Tufro, Alda, Hildebrandt, Friedhelm
Publicado 2016