Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

by 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
Published in Kidney international

Electronic Alerts to Identify Acute Kidney Injury in Children: Promises and Pitfalls

by Somers, Michael J.G., Traum, Avram Z.
Published in The Journal of pediatrics

A hemodialysis patient with difficulty ambulating: Answers

by Mann, Nina, Fayemi, Annemarie, Myles, Melissa, Kelley, Nicole, Carmine, Brian, Richmond, Camilla, Traum, Avram Z.
Published in Pediatric nephrology (Berlin, West)

A hemodialysis patient with difficulty ambulating: Questions

by Mann, Nina, Fayemi, Annemarie, Myles, Melissa, Kelley, Nicole, Carmine, Brian, Richmond, Camilla, Traum, Avram Z.
Published in Pediatric nephrology (Berlin, West)

Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients

by Mann, Nina, Braun, Daniela A, Amann, Kassaundra, Tan, Weizhen, Shril, Shirlee, Connaughton, Dervla M, Nakayama, Makiko, Schneider, Ronen, Kitzler, Thomas M, van der Ven, Amelie T, Chen, Jing, Ityel, Hadas, Vivante, Asaf, Majmundar, Amar J, Daga, Ankana, Warejko, Jillian K, Lovric, Svjetlana, Ashraf, Shazia, Jobst-Schwan, Tilman, Widmeier, Eugen, Hugo, Hannah, Mane, Shrikant M, Spaneas, Leslie, Somers, Michael J G, Ferguson, Michael A, Traum, Avram Z, Stein, Deborah R, Baum, Michelle A, Daouk, Ghaleb H, Lifton, Richard P, Manzi, Shannon, Vakili, Khashayar, Kim, Heung Bae, Rodig, Nancy M, Hildebrandt, Friedhelm
Published in Journal of the American Society of Nephrology

Clinical significance of incidentally discovered renal cysts in pediatric patients

by Botwin, Ariel, Phewplung, Teerasak, Wu, Kaiming, Lim, Ruth, Traum, Avram Z., Gee, Michael S.
Published in Abdominal radiology (New York)

Survival of neonates born with kidney failure during the initial hospitalization

by Claes, Donna J., Richardson, Troy, Harer, Matthew W., Keswani, Mahima, Neu, Alicia, Mahon, Allison C. Redpath, Somers, Michael J., Traum, Avram Z., Warady, Bradley A.
Published in Pediatric nephrology (Berlin, West)

Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT

by Seltzsam, Steve, Wang, Chunyan, Zheng, Bixia, Mann, Nina, Connaughton, Dervla M., Wu, Chen-Han Wilfred, Schneider, Sophia, Schierbaum, Luca, Kause, Franziska, Kolvenbach, Caroline M., Nakayama, Makiko, Dai, Rufeng, Ottlewski, Isabel, Schneider, Ronen, Deutsch, Konstantin, Buerger, Florian, Klämbt, Verena, Mao, Youying, Onuchic-Whitford, Ana C., Nicolas-Frank, Camille, Yousef, Kirollos, Pantel, Dalia, Lai, Ethan W., Salmanullah, Daanya, Majmundar, Amar J., Bauer, Stuart B., Rodig, Nancy M., Somers, Michael J.G., Traum, Avram Z., Stein, Deborah R., Daga, Ankana, Baum, Michelle A., Daouk, Ghaleb H., Tasic, Velibor, Awad, Hazem S., Eid, Loai A., El Desoky, Sherif, Shalaby, Mohammed, Kari, Jameela A., Fathy, Hanan M., Soliman, Neveen A., Mane, Shrikant M., Shril, Shirlee, Ferguson, Michael A., Hildebrandt, Friedhelm
Published in Genetics in medicine

Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome

by Warejko, Jillian K, Schueler, Markus, Vivante, Asaf, Tan, Weizhen, Daga, Ankana, Lawson, Jennifer A, Braun, Daniela A, Shril, Shirlee, Amann, Kassaundra, Somers, Michael J.G, Rodig, Nancy M, Baum, Michelle A, Daouk, Ghaleb, Traum, Avram Z, Kim, Heung Bae, Vakili, Khashayar, Porras, Diego, Lock, James, Rivkin, Michael J, Chaudry, Gulraiz, Smoot, Leslie B, Singh, Michael N, Smith, Edward R, Mane, Shrikant M, Lifton, Richard P, Stein, Deborah R, Ferguson, Michael A, Hildebrandt, Friedhelm
Published in Hypertension (Dallas, Tex. 1979)

Parenteral Fluid Therapy in Children

by Traum, Avram Z., Somers, Michael J. G.
Published in Current treatment options in pediatrics

Promoting Emotional Well-Being Through an Innovative Personal and Professional Development Curriculum for Pediatric Residents

by Hata, Susan R., Dzara, Kristina, Meyer, Robert, Traum, Avram Z., Scott-Vernaglia, Shannon
Published in Medical science educator

Urine proteomic profiling of pediatric nephrotic syndrome

by Khurana, Mona, Traum, Avram Z, Aivado, Manuel, Wells, Meghan P, Guerrero, Manuel, Grall, Franck, Libermann, Towia A, Schachter, Asher D
Published in Pediatric nephrology (Berlin, West)

The Need for Tolerance in Pediatric Organ Transplantation

by Traum, Avram Z, Kawai, Tatsuo, Vacanti, Joseph P, Sachs, David H, Cosimi, A. Benedict, Madsen, Joren C
Published in Pediatrics (Evanston)

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

by Warejko, Jillian K, Tan, Weizhen, Daga, Ankana, Schapiro, David, Lawson, Jennifer A, Shril, Shirlee, Lovric, Svjetlana, Ashraf, Shazia, Rao, Jia, Hermle, Tobias, Jobst-Schwan, Tilman, Widmeier, Eugen, Majmundar, Amar J, Schneider, Ronen, Gee, Heon Yung, Schmidt, J Magdalena, Vivante, Asaf, van der Ven, Amelie T, Ityel, Hadas, Chen, Jing, Sadowski, Carolin E, Kohl, Stefan, Pabst, Werner L, Nakayama, Makiko, Somers, Michael J G, Rodig, Nancy M, Daouk, Ghaleb, Baum, Michelle, Stein, Deborah R, Ferguson, Michael A, Traum, Avram Z, Soliman, Neveen A, Kari, Jameela A, El Desoky, Sherif, Fathy, Hanan, Zenker, Martin, Bakkaloglu, Sevcan A, Müller, Dominik, Noyan, Aytul, Ozaltin, Fatih, Cadnapaphornchai, Melissa A, Hashmi, Seema, Hopcian, Jeffrey, Kopp, Jeffrey B, Benador, Nadine, Bockenhauer, Detlef, Bogdanovic, Radovan, Stajić, Nataša, Chernin, Gil, Ettenger, Robert, Fehrenbach, Henry, Kemper, Markus, Munarriz, Reyner Loza, Podracka, Ludmila, Büscher, Rainer, Serdaroglu, Erkin, Tasic, Velibor, Mane, Shrikant, Lifton, Richard P, Braun, Daniela A, Hildebrandt, Friedhelm
Published in Clinical journal of the American Society of Nephrology

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract

by 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
Published in Journal of the American Society of Nephrology

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

by Connaughton, Dervla M., Dai, Rufeng, Owen, Danielle J., Marquez, Jonathan, Mann, Nina, Graham-Paquin, Adda L., Nakayama, Makiko, Coyaud, Etienne, Laurent, Estelle M.N., St-Germain, Jonathan R., Blok, Lot Snijders, Vino, Arianna, Klämbt, Verena, Deutsch, Konstantin, Wu, Chen-Han Wilfred, Kolvenbach, Caroline M., Kause, Franziska, Ottlewski, Isabel, Schneider, Ronen, Kitzler, Thomas M., Majmundar, Amar J., Buerger, Florian, Onuchic-Whitford, Ana C., Youying, Mao, Kolb, Amy, Salmanullah, Daanya, Chen, Evan, van der Ven, Amelie T., Rao, Jia, Ityel, Hadas, Seltzsam, Steve, Rieke, Johanna M., Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Kohl, Stefan, Dworschak, Gabriel C., Hermle, Tobias, Alders, Mariëlle, Bartolomaeus, Tobias, Bauer, Stuart B., Baum, Michelle A., Brilstra, Eva H., Challman, Thomas D., Zyskind, Jacob, Costin, Carrie E., Dipple, Katrina M., Duijkers, Floor A., Ferguson, Marcia, Fitzpatrick, David R., Fick, Roger, Glass, Ian A., Hulick, Peter J., Kline, Antonie D., Krey, Ilona, Kumar, Selvin, Lu, Weining, Marco, Elysa J., Wentzensen, Ingrid M., Mefford, Heather C., Platzer, Konrad, Povolotskaya, Inna S., Savatt, Juliann M., Shcherbakova, Natalia V., Senguttuvan, Prabha, Squire, Audrey E., Stein, Deborah R., Thiffault, Isabelle, Voinova, Victoria Y., Somers, Michael J.G., Ferguson, Michael A., Traum, Avram Z., Daouk, Ghaleb H., Daga, Ankana, Rodig, Nancy M., Terhal, Paulien A., van Binsbergen, Ellen, Eid, Loai A., Tasic, Velibor, Rasouly, Hila Milo, Lim, Tze Y., Ahram, Dina F., Gharavi, Ali G., Reutter, Heiko M., Rehm, Heidi L., MacArthur, Daniel G., Lek, Monkol, Laricchia, Kristen M., Lifton, Richard P., Xu, Hong, Mane, Shrikant M., Sanna-Cherchi, Simone, Sharrocks, Andrew D., Raught, Brian, Fisher, Simon E., Bouchard, Maxime, Khokha, Mustafa K., Shril, Shirlee, Hildebrandt, Friedhelm
Published in American journal of human genetics

The need for tolerance in pediatric organ transplantation

by Traum, Avram Z, Kawai, Tatsuo, Vacanti, Joseph P, Sachs, David H, Cosimi, A. Benedict, Madsen, Joren C
Published in Pediatrics (Evanston)