ScholarIQanswers from OpenAlex & ORCID
Howard Trachtman
ResearcherPublications, citations & collaboration network
Howard Trachtman is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Howard Trachtman have?
ScholarIQindexed works
Howard Trachtman has 511 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Howard Trachtman have?
ScholarIQcitation count
Howard Trachtman has 19,442 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Howard Trachtman?
ScholarIQh-index
Howard Trachtman has an h-index of 68 in OpenAlex.
What is the i10-index of Howard Trachtman?
ScholarIQi10-index
Howard Trachtman has an i10-index of 246 in OpenAlex.
What is the ORCID of Howard Trachtman?
ScholarIQorcid
The ORCID for Howard Trachtman is on the source record.
What is the OpenAlex record for Howard Trachtman?
ScholarIQopenalex
The OpenAlex for Howard Trachtman is on the source record.
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
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
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
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
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