ScholarIQanswers from OpenAlex & ORCID
Carol Nelson‐Williams
ResearcherPublications, citations & collaboration network
Carol Nelson‐Williams is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Carol Nelson‐Williams have?
ScholarIQindexed works
Carol Nelson‐Williams has 120 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Carol Nelson‐Williams have?
ScholarIQcitation count
Carol Nelson‐Williams has 18,833 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Carol Nelson‐Williams?
ScholarIQh-index
Carol Nelson‐Williams has an h-index of 48 in OpenAlex.
What is the i10-index of Carol Nelson‐Williams?
ScholarIQi10-index
Carol Nelson‐Williams has an i10-index of 79 in OpenAlex.
What is the ORCID of Carol Nelson‐Williams?
ScholarIQorcid
The ORCID for Carol Nelson‐Williams is on the source record.
What is the OpenAlex record for Carol Nelson‐Williams?
ScholarIQopenalex
The OpenAlex for Carol Nelson‐Williams is on the source record.
What are the most-cited papers on Carol Nelson‐Williams?
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
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
Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism
Ute I. Scholl, Gerald Goh, Gabriel Stölting, Regina Campos de Oliveira, Murim Choi, John D. Overton, Annabelle L. Fonseca, Reju Korah, Lee F. Starker, John W. Kunstman, Manju L. Prasad, Erum A. Hartung, Nelly Mauras, Matthew Benson, Tammy M. Brady, Jay R. Shapiro, Erin Loring, Carol Nelson‐Williams, Steven K. Libutti, Shrikant Mane, Per Hellman, Gunnar Westin, Göran Åkerström, Peyman Björklund, Tobias Carling, Christoph Fahlke, Patricia Hidalgo, Richard P. Lifton
Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism
Ute I. Scholl, Gabriel Stölting, Carol Nelson‐Williams, Alfred A. Vichot, Murim Choi, Erin Loring, Manju L. Prasad, Gerald Goh, Tobias Carling, C. Christofer Juhlin, Ivo Quack, Lars Christian Rump, Anne Thiel, Marc B. Lande, Britney G Frazier, Majid Rasoulpour, David L Bowlin, Christine B. Sethna, Howard Trachtman, Christoph Fahlke, Richard P. Lifton
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23
Ali G. Gharavi, Yan Yan, Francesco Scolari, Francesco Paolo Schena, Giovanni M. Frascà, Gian Marco Ghiggeri, Kerry Cooper, Antonio Amoroso, Battista Fabio Viola, Graziana Battini, Gianluca Caridi, Cristina Canova, Anita Farhi, V. S. Subramanian, Carol Nelson‐Williams, Sue Woodford, Bruce A. Julian, Robert Wyatt, Richard P. Lifton