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How has Howard Trachtman's publication output changed over time?
ScholarIQpublication output · 1997–2023
Output grew0% over the shown period — from 1 works in 1997 to 1 in 2023.
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1997200720082009201120122013201520222023
What are the most-cited papers on Howard Trachtman?
ScholarIQmost cited works
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
David B. Simon, Ranjit S. Bindra, Traci A. Mansfield, Carol Nelson‐Williams, Érica Mendonça, Rosário Stone, Scott J. Schurman, Ahmet Nayır, Harika Alpay, A Bakkaloğlu, Juan Rodríguez‐Soriano, José Manuel Morales, Sami A. Sanjad, Carol M. Taylor, Daniela T. Pilz, Andrew S. Brem, Howard Trachtman, William R. Griswold, George A. Richard, Eunice John, Richard P. Lifton
S137905309. 1997870 Citations
APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy
Jeffrey B. Kopp, George W. Nelson, Karmini Sampath, Randall C. Johnson, Giulio Genovese, Ping An, David J. Friedman, W Briggs, Richard A. Dart, Stephen M. Korbet, Michele H. Mokrzycki, Paul L. Kimmel, Sophie Limou, Tejinder S. Ahuja, Jeffrey S. Berns, Justyna Fryc, Eric E. Simon, Michael C. Smith, Howard Trachtman, Donna M. Michel, Jeffrey R. Schelling, David Vlahov, Martin R. Pollak, Cheryl A. Winkler
Journal of the American Society of Nephrology. 2011862 CitationsOPEN ACCESS
Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK
David B. Simon, Fiona E. Karet, Juan Rodríguez‐Soriano, Jahed Hamdan, Antonio DiPietro, Howard Trachtman, Sami A. Sanjad, Richard P. Lifton
S137905309. 1996827 Citations
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis
Jeffrey B. Kopp, Michael W. Smith, George W. Nelson, Randall C. Johnson, Barry I. Freedman, Donald W. Bowden, Tarás K. Oleksyk, Louise M. McKenzie, Hiroshi Kajiyama, Tejinder S. Ahuja, Jeffrey S. Berns, W Briggs, Monique E. Cho, Richard A. Dart, Paul L. Kimmel, Stephen M. Korbet, Donna M. Michel, Michele H. Mokrzycki, Jeffrey R. Schelling, Eric E. Simon, Howard Trachtman, David Vlahov, Cheryl A. Winkler
S137905309. 2008713 Citations
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
Lynn M. Boyden, Murim Choi, Keith A. Choate, Carol Nelson‐Williams, Anita Farhi, Hakan R. Toka, Irina R. Tikhonova, Robert Bjornson, Shrikant Mane, Giacomo Colussi, Marcel Lebel, Richard D. Gordon, Ben A. Semmekrot, A. Poujol, Matti Välimäki, Maria Elisabetta De Ferrari, Sami A. Sanjad, Michael Gutkin, Fiona E. Karet, Joseph Tucci, Jim Stockigt, Kim M. Keppler‐Noreuil, Craig Porter, Sudhir Anand, Margo L. Whiteford, Ira D. Davis, Stephanie Dewar, Alberto Bettinelli, Jeffrey J. Fadrowski, Craig W. Belsha, Tracy E. Hunley, Raoul D. Nelson, Howard Trachtman, Trevor Cole, Maury Pinsk, Detlef Böckenhauer, Mohan Shenoy, Priya Vaidyanathan, John W. Foreman, Majid Rasoulpour, Farook Thameem, Hania Z. Al-Shahrouri, Jai Radhakrishnan, Ali G. Gharavi, Béatrice Goilav, Richard P. Lifton
Nature. 2012638 Citations
Related on ScholarIQ
University of Michigan
Institution
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
Paper
APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy
Paper
Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMK
Paper
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis
Paper
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
Paper