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Nathaniel Rothman

ResearcherPublications, citations & collaboration network

Nathaniel Rothman is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Nathaniel Rothman have?

ScholarIQindexed works

Nathaniel Rothman has 1,210 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Nathaniel Rothman have?

ScholarIQcitation count

Nathaniel Rothman has 36,924 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Nathaniel Rothman?

ScholarIQh-index

Nathaniel Rothman has an h-index of 101 in OpenAlex.

What is the i10-index of Nathaniel Rothman?

ScholarIQi10-index

Nathaniel Rothman has an i10-index of 470 in OpenAlex.

What is the ORCID of Nathaniel Rothman?

ScholarIQorcid

The ORCID for Nathaniel Rothman is on the source record.

What is the OpenAlex record for Nathaniel Rothman?

ScholarIQopenalex

The OpenAlex for Nathaniel Rothman is on the source record.

What are the most-cited papers on Nathaniel Rothman?

ScholarIQmost cited works
International patterns and trends in thyroid cancer incidence, 1973–2002
Briseis A. Kilfoy, Tongzhang Zheng, Theodore R. Holford, Xuesong Han, Mary H. Ward, Andreas Sjödin, Yaqun Zhang, Yaqun Zhang, Yana Bai, Cairong Zhu, Grace L. Guo, Nathaniel Rothman, Yawei Zhang, Yawei Zhang
Cancer Causes & Control. 2008719 CitationsOPEN ACCESS
Hematotoxicity in Workers Exposed to Low Levels of Benzene
Qing Lan, Luoping Zhang, Guilan Li, Roel Vermeulen, Rona Singer Weinberg, Mustafa Dosemeci, Stephen M. Rappaport, Min Shen, Blanche P. Alter, Yongji Wu, William Kopp, Suramya Waidyanatha, Charles S. Rabkin, Weihong Guo, Stephen J. Chanock, Richard B. Hayes, Martha S. Linet, Sungkyoon Kim, Songnian Yin, Nathaniel Rothman, Martyn T. Smith
Science. 2004629 CitationsOPEN ACCESS
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Nathaniel Rothman, Montserrat García‐Closas, Nilanjan Chatterjee, Núria Malats, Xifeng Wu, Jonine D. Figueroa, Francisco X. Real, David Van Den Berg, Giuseppe Matullo, Dalsu Baris, Michael J. Thun, Lambertus A. Kiemeney, Paolo Vineis, Immaculata De Vivo, Demetrius Albanes, Mark P. Purdue, Þórunn Rafnar, Michelle A.T. Hildebrandt, Anne E. Kiltie, Olivier Cussenot, Klaus Golka, Rajiv Kumar, Jack A. Taylor, José Mayordomo, Kevin B. Jacobs, Manolis Kogevinas, Amy Hutchinson, Zhaoming Wang, Yi‐Ping Fu, Ludmila Prokunina‐Olsson, Laurie Burdett, Meredith Yeager, William Wheeler, Adonina Tardón, Cònsol Serra, Alfredo Carrato, Reina García-Closas, Josep Lloreta, Alison Johnson, Molly Schwenn, Margaret R. Karagas, Alan R. Schned, Gerald L. Andriole, Robert L. Grubb, Amanda Black, Eric J. Jacobs, W. Ryan Diver, Susan M. Gapstur, Stephanie J. Weinstein, Jarmo Virtamo, Victoria K. Cortessis, Manuela Gago-Domínguez, Malcolm C. Pike, Mariana C. Stern, Jian‐Min Yuan, David J. Hunter, Monica McGrath, Colin P. Dinney, Bogdan Czerniak, Meng Chen, Hushan Yang, Sita H. Vermeulen, Katja K.H. Aben, J.A. Witjes, Remco R. Makkinje, Patrick Sulem, Søren Besenbacher, Kāri Stefánsson, Elio Ríboli, Paul Brennan, Salvatore Panico, Carmen Navarro, Naomi E. Allen, H. Bas Bueno-de-Mesquita, Dimitrios Trichopoulos, Neil E. Caporaso, Maria Teresa Landi, Federico Canzian, Börje Ljungberg, Anne Tjønneland, Françoise Clavel‐Chapelon, D. Timothy Bishop, Mark Teo, Margaret A. Knowles, Simonetta Guarrera, Silvia Polidoro, Fulvio Ricceri, Carlotta Sacerdote, Alessandra Allione, Géraldine Cancel‐Tassin, Silvia Selinski, Jan G. Hengstler, H. Dietrich, Tony Fletcher, Péter Rudnai, Eugen Gurzău, Kvetoslava Koppová, Sophia C.E. Bolick, Ashley C. Godfrey, Zongli Xu
Nature Genetics. 2010489 CitationsOPEN ACCESS
Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium
Nathaniel Rothman, Christine F. Skibola, Sophia Wang, Gareth J. Morgan, Qing Lan, Martyn T. Smith, John J. Spinelli, Eleanor V. Willett, Sílvia de Sanjosé, Pierluigi Cocco, Sonja I. Berndt, Paul Brennan, Angela Brooks‐Wilson, Sholom Wacholder, Nikolaus Becker, Patricia Hartge, Tongzhang Zheng, Eve Roman, Elizabeth A. Holly, Paolo Boffetta, Bruce K. Armstrong, Wendy Cozen, Martha S. Linet, F. Xavier Bosch, Maria Grazia Ennas, Theodore R. Holford, Richard P. Gallagher, Sara Rollinson, Paige M. Bracci, James R. Cerhan, Denise Whitby, Patrick S. Moore, Brian P. Leaderer, Agnes S. Lai, Charlotte F. Spink, S. Scott Davis, Ramón Bosch, Aldo Scarpa, Yawei Zhang, Richard K. Severson, Meredith Yeager, Stephen J. Chanock, Alexandra Nieters
The Lancet Oncology. 2005380 Citations
Mosaic loss of chromosome Y is associated with common variation near TCL1A
Weiyin Zhou, Mitchell J. Machiela, Neal D. Freedman, Nathaniel Rothman, Núria Malats, Casey Dagnall, Neil E. Caporaso, Lauren T. Teras, Mia M. Gaudet, Susan M. Gapstur, Victoria L. Stevens, Kevin B. Jacobs, Joshua N. Sampson, Demetrius Albanes, Stephanie J. Weinstein, Jarmo Virtamo, Sonja I. Berndt, Robert N. Hoover, Amanda Black, Debra T. Silverman, Jonine D. Figueroa, Montserrat García‐Closas, Francisco X. Real, Julie Earl, Gaëlle Marenne, Benjamín Rodríguez‐Santiago, Margaret R. Karagas, Alison Johnson, Molly Schwenn, Xifeng Wu, Jian Gu, Yuanqing Ye, Amy Hutchinson, Margaret A. Tucker, Luis A. Pérez‐Jurado, Michael Dean, Meredith Yeager, Stephen J. Chanock
Nature Genetics. 2016242 Citations

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