Chad Huff

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Chad Huff

Professor

 https://orcid.org/0000-0002-1100-9364

    • 6767 Bertner Ave, Mitchell Basic Science Research Building

      77030 Houston

      United States

    Calculated based on number of publications stored in Pure and citations from Scopus
    20072024

    Research activity per year

    Search results

    • 2024

      A west African ancestry-associated SNP on 8q24 predicts a positive biopsy in African American men with suspected prostate cancer following PSA screening

      Gu, J., Chery, L., González, G. M. N., Huff, C., Strom, S., Jones, J. A., Griffith, D. P., Canfield, S. E., Wang, X., Huang, X., Roberson, P., Meng, Q. H., Troncoso, P., Ittmann, M., Covinsky, M., Scheurer, M., Irizarry Ramirez, M. & Pettaway, C. A., 2024, (Accepted/In press) In: Prostate.

      Research output: Contribution to journal › Article › peer-review

    • 2023

      Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

      The Biobank Japan Project, Dec 2023, In: Nature Genetics. 55, 12, p. 2065-2074 10 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      4 Scopus citations

    • Clonal hematopoiesis and risk of prostate cancer in large samples of European ancestry men

      Wang, A., Xu, Y., Yu, Y., Nead, K. T., Kim, T. B., Xu, K., Dadaev, T., Saunders, E., Sheng, X., Wan, P., Pooler, L., Xia, L. Y., Chanock, S., Berndt, S. I., Gapstur, S. M., Stevens, V., Albanes, D., Weinstein, S. J., Gnanapragasam, V., Giles, G. G., & 19 othersNguyen-Dumont, T., Milne, R. L., Pomerantz, M. M., Schmidt, J. A., Stopsack, K. H., Mucci, L. A., Catalona, W. J., Hetrick, K. N., Doheny, K. F., MacInnis, R. J., Southey, M. C., Eeles, R. A., Wiklund, F., Kote-Jarai, Z., Smith, A. J., Conti, D. V., Huff, C., Haiman, C. A. & Darst, B. F., Feb 1 2023, In: Human molecular genetics. 32, 3, p. 489-495 7 p.

      Research output: Contribution to journal › Article › peer-review

      1 Scopus citations

    • Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry

      NC-LA PCaP Investigators & Canary PASS Investigators, Jul 6 2023, In: American journal of human genetics. 110, 7, p. 1200-1206 7 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      2 Scopus citations

    • Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry

      Chen, F., Madduri, R. K., Rodriguez, A. A., Darst, B. F., Chou, A., Sheng, X., Wang, A., Shen, J., Saunders, E. J., Rhie, S. K., Bensen, J. T., Ingles, S. A., Kittles, R. A., Strom, S. S., Rybicki, B. A., Nemesure, B., Isaacs, W. B., Stanford, J. L., Zheng, W., Sanderson, M., & 98 othersJohn, E. M., Park, J. Y., Xu, J., Wang, Y., Berndt, S. I., Huff, C. D., Yeboah, E. D., Tettey, Y., Lachance, J., Tang, W., Rentsch, C. T., Cho, K., Mcmahon, B. H., Biritwum, R. B., Adjei, A. A., Tay, E., Truelove, A., Niwa, S., Sellers, T. A., Yamoah, K., Murphy, A. B., Crawford, D. C., Patel, A. V., Bush, W. S., Aldrich, M. C., Cussenot, O., Petrovics, G., Cullen, J., Neslund-Dudas, C. M., Stern, M. C., Kote-Jarai, Z., Govindasami, K., Cook, M. B., Chokkalingam, A. P., Hsing, A. W., Goodman, P. J., Hoffmann, T. J., Drake, B. F., Hu, J. J., Keaton, J. M., Hellwege, J. N., Clark, P. E., Jalloh, M., Gueye, S. M., Niang, L., Ogunbiyi, O., Idowu, M. O., Popoola, O., Adebiyi, A. O., Aisuodionoe-Shadrach, O. I., Ajibola, H. O., Jamda, M. A., Oluwole, O. P., Nwegbu, M., Adusei, B., Mante, S., Darkwa-Abrahams, A., Mensah, J. E., Diop, H., Van Den Eeden, S. K., Blanchet, P., Fowke, J. H., Casey, G., Hennis, A. J., Lubwama, A., Thompson, I. M., Leach, R., Easton, D. F., Preuss, M. H., Loos, R. J., Gundell, S. M., Wan, P., Mohler, J. L., Fontham, E. T., Smith, G. J., Taylor, J. A., Srivastava, S., Eeles, R. A., Carpten, J. D., Kibel, A. S., Multigner, L., Parent, M. É., Menegaux, F., Cancel-Tassin, G., Klein, E. A., Andrews, C., Rebbeck, T. R., Brureau, L., Ambs, S., Edwards, T. L., Watya, S., Chanock, S. J., Witte, J. S., Blot, W. J., Michael Gaziano, J., Justice, A. C., Conti, D. V. & Haiman, C. A., Jul 2023, In: European urology. 84, 1, p. 13-21 9 p.

      Research output: Contribution to journal › Article › peer-review

      9 Scopus citations

    • Germline genetic variants and pediatric rhabdomyosarcoma outcomes: a report from the Children's Oncology Group

      Martin-Giacalone, B. A., Richard, M. A., Scheurer, M. E., Khan, J., Sok, P., Shetty, P. B., Chanock, S. J., Li, S. A., Yeager, M., Marquez-Do, D. A., Barkauskas, D. A., Hall, D., McEvoy, M. T., Brown, A. L., Sabo, A., Scheet, P., Huff, C. D., Skapek, S. X., Hawkins, D. S., Venkatramani, R., & 2 othersMirabello, L. & Lupo, P. J., Jun 8 2023, In: Journal of the National Cancer Institute. 115, 6, p. 733-741 9 p.

      Research output: Contribution to journal › Article › peer-review

      2 Scopus citations

    • Germline Sequencing Analysis to Inform Clinical Gene Panel Testing for Aggressive Prostate Cancer

      Darst, B. F., Saunders, E., Dadaev, T., Sheng, X., Wan, P., Pooler, L., Xia, L. Y., Chanock, S., Berndt, S. I., Wang, Y., Patel, A. V., Albanes, D., Weinstein, S. J., Gnanapragasam, V., Huff, C., Couch, F. J., Wolk, A., Giles, G. G., Nguyen-Dumont, T., Milne, R. L., & 17 othersPomerantz, M. M., Schmidt, J. A., Travis, R. C., Key, T. J., Stopsack, K. H., Mucci, L. A., Catalona, W. J., Marosy, B., Hetrick, K. N., Doheny, K. F., Macinnis, R. J., Southey, M. C., Eeles, R. A., Wiklund, F., Conti, D. V., Kote-Jarai, Z. & Haiman, C. A., Nov 16 2023, In: JAMA Oncology. 9, 11, p. 1514-1524 11 p.

      Research output: Contribution to journal › Article › peer-review

      2 Scopus citations

    • RAB1A haploinsufficiency phenocopies the 2p14–p15 microdeletion and is associated with impaired neuronal differentiation

      Rios, J. J., Li, Y., Paria, N., Bohlender, R. J., Huff, C., Rosenfeld, J. A., Liu, P., Bi, W., Haga, K., Fukuda, M., Vashisth, S., Kaur, K., Chahrour, M. H., Bober, M. B., Duker, A. L., Ladha, F. A., Hanchard, N. A., Atala, K., Khanshour, A. M., Smith, L., & 2 othersWise, C. A. & Delgado, M. R., Dec 7 2023, In: American journal of human genetics. 110, 12, p. 2103-2111 9 p.

      Research output: Contribution to journal › Article › peer-review

      1 Scopus citations

    • Rewired m6A epitranscriptomic networks link mutant p53 to neoplastic transformation

      Xu, A., Liu, M., Huang, M. F., Zhang, Y., Hu, R., Gingold, J. A., Liu, Y., Zhu, D., Chien, C. S., Wang, W. C., Liao, Z., Yuan, F., Hsu, C. W., Tu, J., Yu, Y., Rosen, T., Xiong, F., Jia, P., Yang, Y. P., Bazer, D. A., & 13 othersChen, Y. W., Li, W., Huff, C. D., Zhu, J. J., Aguilo, F., Chiou, S. H., Boles, N. C., Lai, C. C., Hung, M. C., Zhao, Z., Van Nostrand, E. L., Zhao, R. & Lee, D. F., Dec 2023, In: Nature communications. 14, 1, 1694.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      3 Scopus citations
    • 2022

      A Rare Germline HOXB13 Variant Contributes to Risk of Prostate Cancer in Men of African Ancestry

      Darst, B. F., Hughley, R., Pfennig, A., Hazra, U., Fan, C., Wan, P., Sheng, X., Xia, L., Andrews, C., Chen, F., Berndt, S. I., Kote-Jarai, Z., Govindasami, K., Bensen, J. T., Ingles, S. A., Rybicki, B. A., Nemesure, B., John, E. M., Fowke, J. H., Huff, C. D., & 81 othersStrom, S. S., Isaacs, W. B., Park, J. Y., Zheng, W., Ostrander, E. A., Walsh, P. C., Carpten, J., Sellers, T. A., Yamoah, K., Murphy, A. B., Sanderson, M., Crawford, D. C., Gapstur, S. M., Bush, W. S., Aldrich, M. C., Cussenot, O., Petrovics, G., Cullen, J., Neslund-Dudas, C., Kittles, R. A., Xu, J., Stern, M. C., Chokkalingam, A. P., Multigner, L., Parent, M. E., Menegaux, F., Cancel-Tassin, G., Kibel, A. S., Klein, E. A., Goodman, P. J., Stanford, J. L., Drake, B. F., Hu, J. J., Clark, P. E., Blanchet, P., Casey, G., Hennis, A. J. M., Lubwama, A., Thompson, I. M., Leach, R. J., Gundell, S. M., Pooler, L., Mohler, J. L., Fontham, E. T. H., Smith, G. J., Taylor, J. A., Brureau, L., Blot, W. J., Biritwum, R., Tay, E., Truelove, A., Niwa, S., Tettey, Y., Varma, R., McKean-Cowdin, R., Torres, M., Jalloh, M., Magueye Gueye, S., Niang, L., Ogunbiyi, O., Oladimeji Idowu, M., Popoola, O., Adebiyi, A. O., Aisuodionoe-Shadrach, O. I., Nwegbu, M., Adusei, B., Mante, S., Darkwa-Abrahams, A., Yeboah, E. D., Mensah, J. E., Anthony Adjei, A., Diop, H., Cook, M. B., Chanock, S. J., Watya, S., Eeles, R. A., Chiang, C. W. K., Lachance, J., Rebbeck, T. R., Conti, D. V. & Haiman, C. A., May 2022, In: European urology. 81, 5, p. 458-462 5 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      16 Scopus citations

    • A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic cancer risk

      Yu, Y., Chang, K., Chen, J. S., Bohlender, R. J., Fowler, J., Zhang, D., Huang, M., Chang, P., Li, Y., Wong, J., Wang, H., Gu, J., Wu, X., Schildkraut, J., Cannon-Albright, L., Ye, Y., Zhao, H., Hildebrandt, M. A. T., Permuth, J. B., Li, D., & 2 othersScheet, P. & Huff, C. D., Jan 13 2022, In: Human Genetics and Genomics Advances. 3, 1, 100078.

      Research output: Contribution to journal › Article › peer-review

      Open Access

    • Copy number variants are ovarian cancer risk alleles at known and novel risk loci

      Devries, A. A., Dennis, J., Tyrer, J. P., Peng, P. C., Coetzee, S. G., Reyes, A. L., Plummer, J. T., Davis, B. D., Chen, S. S., Dezem, F. S., Aben, K. K. H., Anton-Culver, H., Antonenkova, N. N., Beckmann, M. W., Beeghly-Fadiel, A., Berchuck, A., Bogdanova, N. V., Bogdanova-Markov, N., Brenton, J. D., Butzow, R., & 68 othersCampbell, I., Chang-Claude, J., Chenevix-Trench, G., Cook, L. S., Defazio, A., Doherty, J. A., Dork, T., Eccles, D. M., Eliassen, A. H., Fasching, P. A., Fortner, R. T., Giles, G. G., Goode, E. L., Goodman, M. T., Gronwald, J., Hakansson, N., Hildebrandt, M. A. T., Huff, C., Huntsman, D. G., Jensen, A., Kar, S., Karlan, B. Y., Khusnutdinova, E. K., Kiemeney, L. A., Kjaer, S. K., Kupryjanczyk, J., Labrie, M., Lambrechts, D., Le, N. D., Lubinski, J., May, T., Menon, U., Milne, R. L., Modugno, F., Monteiro, A. N., Moysich, K. B., Odunsi, K., Olsson, H., Pearce, C. L., Pejovic, T., Ramus, S. J., Riboli, E., Riggan, M. J., Romieu, I., Sandler, D. P., Schildkraut, J. M., Setiawan, V. W., Sieh, W., Song, H., Sutphen, R., Terry, K. L., Thompson, P. J., Titus, L., Tworoger, S. S., Van Nieuwenhuysen, E., Edwards, D. V., Webb, P. M., Wentzensen, N., Whittemore, A. S., Wolk, A., Wu, A. H., Ziogas, A., Freedman, M. L., Lawrenson, K., Pharoah, P. D. P., Easton, D. F., Gayther, S. A. & Jones, M. R., Nov 1 2022, In: Journal of the National Cancer Institute. 114, 11, p. 1533-1544 12 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      3 Scopus citations

    • Erratum: Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk (European journal of human genetics : EJHG (2022) 30 3 (349-362))

      GEMO Study Collaborators, GC-HBOC Study Collaborators, EMBRACE Collaborators, OPAL study group, AOCS Group, KConFab investigators, HEBON Investigators, OCAC Consortium & CIMBA Consortium, May 1 2022, In: European journal of human genetics : EJHG. 30, 5, p. 630-631 2 p.

      Research output: Contribution to journal › Comment/debate › peer-review

      Open Access
      1 Scopus citations

    • Hereditary retinoblastoma iPSC model reveals aberrant spliceosome function driving bone malignancies

      Tu, J., Huo, Z., Yu, Y., Zhu, D., Xu, A., Huang, M. F., Hu, R., Wang, R., Gingold, J. A., Chen, Y. H., Tsai, K. L., Forcioli-Conti, N. R., Huang, S. X. L., Webb, T. R., Su, J., Bazer, D. A., Jia, P., Yustein, J. T., Wang, L. L., Hung, M. C., & 5 othersZhao, Z., Huff, C. D., Shen, J., Zhao, R. & Lee, D. F., Apr 19 2022, In: Proceedings of the National Academy of Sciences of the United States of America. 119, 16, 2117857119.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      12 Scopus citations

    • Impact of conditioning chemotherapy on lymphocyte kinetics and outcomes in LBCL patients treated with CAR T-cell therapy

      Strati, P., Jallouk, A. P., Sun, R., Choi, J., Das, K., Cherng, H. J., Ahmed, S., Lee, H. J., Iyer, S. P., Nair, R., Nastoupil, L. J., Steiner, R. E., Huff, C. D., Yu, Y., Mistry, H., Pulsifer, B., Noorani, M., Saini, N., Shpall, E. J., Kebriaei, P., & 4 othersFlowers, C. R., Westin, J. R., Hildebrandt, M. A. T. & Neelapu, S. S., Nov 2022, In: Leukemia. 36, 11, p. 2669-2677 9 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      7 Scopus citations

    • Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palate

      Yu, Y., Alvarado, R., Petty, L. E., Bohlender, R. J., Shaw, D. M., Below, J. E., Bejar, N., Ruiz, O. E., Tandon, B., Eisenhoffer, G. T., Kiss, D. L., Huff, C. D., Letra, A. & Hecht, J. T., Jul 15 2022, In: Human molecular genetics. 31, 14, p. 2348-2357 10 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      5 Scopus citations

    • Polygenic risk modeling for prediction of epithelial ovarian cancer risk

      GEMO Study Collaborators, GC-HBOC Study Collaborators, EMBRACE Collaborators, OPAL study group, AOCS Group, KConFab investigators, HEBON Investigators, The OCAC Consortium & the Cimba Consortium, Mar 2022, In: European Journal of Human Genetics. 30, 3, p. 349-362 14 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      19 Scopus citations

    • Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score

      Canary PASS Investigators, The Profile Study Steering Committee, UKGPCS Collaborators, APCB (Australian Prostate Cancer BioResource), NC-LA PCaP Investigators & The IMPACT Study Steering Committee and Collaborators, Apr 2022, In: Prostate Cancer and Prostatic Diseases. 25, 4, p. 755-761 7 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      8 Scopus citations
    • 2021

      Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

      Graff, M., Justice, A. E., Young, K. L., Marouli, E., Zhang, X., Fine, R. S., Lim, E., Buchanan, V., Rand, K., Feitosa, M. F., Wojczynski, M. K., Yanek, L. R., Shao, Y., Rohde, R., Adeyemo, A. A., Aldrich, M. C., Allison, M. A., Ambrosone, C. B., Ambs, S., Amos, C., & 205 othersArnett, D. K., Atwood, L., Bandera, E. V., Bartz, T., Becker, D. M., Berndt, S. I., Bernstein, L., Bielak, L. F., Blot, W. J., Bottinger, E. P., Bowden, D. W., Bradfield, J. P., Brody, J. A., Broeckel, U., Burke, G., Cade, B. E., Cai, Q., Caporaso, N., Carlson, C., Carpten, J., Casey, G., Chanock, S. J., Chen, G., Chen, M., Chen, Y. D. I., Chen, W. M., Chesi, A., Chiang, C. W. K., Chu, L., Coetzee, G. A., Conti, D. V., Cooper, R. S., Cushman, M., Demerath, E., Deming, S. L., Dimitrov, L., Ding, J., Diver, W. R., Duan, Q., Evans, M. K., Falusi, A. G., Faul, J. D., Fornage, M., Fox, C., Freedman, B. I., Garcia, M., Gillanders, E. M., Goodman, P., Gottesman, O., Grant, S. F. A., Guo, X., Hakonarson, H., Haritunians, T., Harris, T. B., Harris, C. C., Henderson, B. E., Hennis, A., Hernandez, D. G., Hirschhorn, J. N., McNeill, L. H., Howard, T. D., Howard, B., Hsing, A. W., Hsu, Y. H. H., Hu, J. J., Huff, C. D., Huo, D., Ingles, S. A., Irvin, M. R., John, E. M., Johnson, K. C., Jordan, J. M., Kabagambe, E. K., Kang, S. J., Kardia, S. L., Keating, B. J., Kittles, R. A., Klein, E. A., Kolb, S., Kolonel, L. N., Kooperberg, C., Kuller, L., Kutlar, A., Lange, L., Langefeld, C. D., Le Marchand, L., Leonard, H., Lettre, G., Levin, A. M., Li, Y., Li, J., Liu, Y., Liu, Y., Liu, S., Lohman, K., Lotay, V., Lu, Y., Maixner, W., Manson, J. A. E., McKnight, B., Meng, Y., Monda, K. L., Monroe, K., Moore, J. H., Mosley, T. H., Mudgal, P., Murphy, A. B., Nadukuru, R., Nalls, M. A., Nathanson, K. L., Nayak, U., N'Diaye, A., Nemesure, B., Neslund-Dudas, C., Neuhouser, M. L., Nyante, S., Ochs-Balcom, H., Ogundiran, T. O., Ogunniyi, A., Ojengbede, O., Okut, H., Olopade, O. I., Olshan, A., Padhukasahasram, B., Palmer, J., Palmer, C. D., Palmer, N. D., Papanicolaou, G., Patel, S. R., Pettaway, C. A., Peyser, P. A., Press, M. F., Rao, D. C., Rasmussen-Torvik, L. J., Redline, S., Reiner, A. P., Rhie, S. K., Rodriguez-Gil, J. L., Rotimi, C. N., Rotter, J. I., Ruiz-Narvaez, E. A., Rybicki, B. A., Salako, B., Sale, M. M., Sanderson, M., Schadt, E., Schreiner, P. J., Schurmann, C., Schwartz, A. G., Shriner, D. A., Signorello, L. B., Singleton, A. B., Siscovick, D. S., Smith, J. A., Smith, S., Speliotes, E., Spitz, M., Stanford, J. L., Stevens, V. L., Stram, A., Strom, S. S., Sucheston, L., Sun, Y. V., Tajuddin, S. M., Taylor, H., Taylor, K., Tayo, B. O., Thun, M. J., Tucker, M. A., Vaidya, D., Van Den Berg, D. J., Vedantam, S., Vitolins, M., Wang, Z., Ware, E. B., Wassertheil-Smoller, S., Weir, D. R., Wiencke, J. K., Williams, S. M., Williams, L. K., Wilson, J. G., Witte, J. S., Wrensch, M., Wu, X., Yao, J., Zakai, N., Zanetti, K., Zemel, B. S., Zhao, W., Zhao, J. H., Zheng, W., Zhi, D., Zhou, J., Zhu, X., Ziegler, R. G., Zmuda, J., Zonderman, A. B., Psaty, B. M., Borecki, I. B., Cupples, L. A., Liu, C. T., Haiman, C. A., Loos, R., Ng, M. C. Y. & North, K. E., Apr 1 2021, In: American journal of human genetics. 108, 4, p. 564-582 19 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      15 Scopus citations

    • Host genetic effects in pneumonia

      Chen, H. H., Shaw, D. M., Petty, L. E., Graff, M., Bohlender, R. J., Polikowsky, H. G., Zhong, X., Kim, D., Buchanan, V. L., Preuss, M. H., Shuey, M. M., Loos, R. J. F., Huff, C. D., Cox, N. J., Bastarache, J. A., Bastarache, L., North, K. E. & Below, J. E., Jan 7 2021, In: American journal of human genetics. 108, 1, p. 194-201 8 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      16 Scopus citations

    • Inhibiting an RBM39/MLL1 epigenomic regulatory complex with dominant-negative peptides disrupts cancer cell transcription and proliferation

      Puvvula, P. K., Yu, Y., Sullivan, K. R., Eyob, H., Rosenberg, J., Welm, A., Huff, C. & Moon, A. M., Jun 1 2021, In: Cell Reports. 35, 9, 109156.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      10 Scopus citations

    • Integrated case-control and somatic-germline interaction analyses of soft-tissue sarcoma

      Hu, F., Yu, Y., Chen, J. S., Hu, H., Scheet, P. & Huff, C. D., Mar 1 2021, In: Journal of medical genetics. 58, 3, p. 145-153 9 p.

      Research output: Contribution to journal › Article › peer-review

      1 Scopus citations

    • Pedigree reconstruction and distant pairwise relatedness estimation from genome sequence data: A demonstration in a population of rhesus macaques (Macaca mulatta)

      Petty, L. E., Phillippi-Falkenstein, K., Kubisch, H. M., Raveendran, M., Harris, R. A., Vallender, E. J., Huff, C. D., Bohm, R. P., Rogers, J. & Below, J. E., May 2021, In: Molecular Ecology Resources. 21, 4, p. 1333-1346 14 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      2 Scopus citations

    • Polygenic hazard score is associated with prostate cancer in multi-ethnic populations

      APCB (Australian Prostate Cancer BioResource), NC-LA PCaP Investigators, The IMPACT Study Steering Committee and Collaborators, Canary PASS Investigators, The Profile Study Steering Committee, The PRACTICAL Consortium & UKGPCS Collaborators, Dec 1 2021, In: Nature communications. 12, 1, 1236.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      32 Scopus citations

    • Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer

      Song, H., Dicks, E. M., Tyrer, J., Intermaggio, M., Chenevix-Trench, G., Bowtell, D. D., Traficante, N., Group, A., Brenton, J., Goranova, T., Hosking, K., Piskorz, A., Van Oudenhove, E., Doherty, J., Harris, H. R., Rossing, M. A., Duerst, M., Dork, T., Bogdanova, N. V., Modugno, F., & 42 othersMoysich, K., Odunsi, K., Ness, R., Karlan, B. Y., Lester, J., Jensen, A., Krüger Kjaer, S., Høgdall, E., Campbell, I. G., Lázaro, C., Pujara, M. A., Cunningham, J., Vierkant, R., Winham, S. J., Hildebrandt, M., Huff, C., Li, D., Wu, X., Yu, Y., Permuth, J. B., Levine, D. A., Schildkraut, J. M., Riggan, M. J., Berchuck, A., Webb, P. M., Group, O. S., Cybulski, C., Gronwald, J., Jakubowska, A., Lubinski, J., Alsop, J., Harrington, P., Chan, I., Menon, U., Pearce, C. L., Wu, A. H., De Fazio, A., Kennedy, C. J., Goode, E., Ramus, S., Gayther, S. & Pharoah, P., May 1 2021, In: Journal of medical genetics. 58, 5, p. 305-313 9 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      29 Scopus citations

    • Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction (Nature Genetics, (2021), 53, 1, (65-75), 10.1038/s41588-020-00748-0)

      Conti, D. V., Darst, B. F., Moss, L. C., Saunders, E. J., Sheng, X., Chou, A., Schumacher, F. R., Olama, A. A. A., Benlloch, S., Dadaev, T., Brook, M. N., Sahimi, A., Hoffmann, T. J., Takahashi, A., Matsuda, K., Momozawa, Y., Fujita, M., Muir, K., Lophatananon, A., Wan, P., & 211 othersLe Marchand, L., Wilkens, L. R., Stevens, V. L., Gapstur, S. M., Carter, B. D., Schleutker, J., Tammela, T. L. J., Sipeky, C., Auvinen, A., Giles, G. G., Southey, M. C., MacInnis, R. J., Cybulski, C., Wokołorczyk, D., Lubiński, J., Neal, D. E., Donovan, J. L., Hamdy, F. C., Martin, R. M., Nordestgaard, B. G., Nielsen, S. F., Weischer, M., Bojesen, S. E., Røder, M. A., Iversen, P., Batra, J., Chambers, S., Moya, L., Horvath, L., Clements, J. A., Tilley, W., Risbridger, G. P., Gronberg, H., Aly, M., Szulkin, R., Eklund, M., Nordström, T., Pashayan, N., Dunning, A. M., Ghoussaini, M., Travis, R. C., Key, T. J., Riboli, E., Park, J. Y., Sellers, T. A., Lin, H. Y., Albanes, D., Weinstein, S. J., Mucci, L. A., Giovannucci, E., Lindstrom, S., Kraft, P., Hunter, D. J., Penney, K. L., Turman, C., Tangen, C. M., Goodman, P. J., Thompson, I. M., Hamilton, R. J., Fleshner, N. E., Finelli, A., Parent, M. É., Stanford, J. L., Ostrander, E. A., Geybels, M. S., Koutros, S., Freeman, L. E. B., Stampfer, M., Wolk, A., Håkansson, N., Andriole, G. L., Hoover, R. N., Machiela, M. J., Sørensen, K. D., Borre, M., Blot, W. J., Zheng, W., Yeboah, E. D., Mensah, J. E., Lu, Y. J., Zhang, H. W., Feng, N., Mao, X., Wu, Y., Zhao, S. C., Sun, Z., Thibodeau, S. N., McDonnell, S. K., Schaid, D. J., West, C. M. L., Burnet, N., Barnett, G., Maier, C., Schnoeller, T., Luedeke, M., Kibel, A. S., Drake, B. F., Cussenot, O., Cancel-Tassin, G., Menegaux, F., Truong, T., Koudou, Y. A., John, E. M., Grindedal, E. M., Maehle, L., Khaw, K. T., Ingles, S. A., Stern, M. C., Vega, A., Gómez-Caamaño, A., Fachal, L., Rosenstein, B. S., Kerns, S. L., Ostrer, H., Teixeira, M. R., Paulo, P., Brandão, A., Watya, S., Lubwama, A., Bensen, J. T., Fontham, E. T. H., Mohler, J., Taylor, J. A., Kogevinas, M., Llorca, J., Castaño-Vinyals, G., Cannon-Albright, L., Teerlink, C. C., Huff, C. D., Strom, S. S., Multigner, L., Blanchet, P., Brureau, L., Kaneva, R., Slavov, C., Mitev, V., Leach, R. J., Weaver, B., Brenner, H., Cuk, K., Holleczek, B., Saum, K. U., Klein, E. A., Hsing, A. W., Kittles, R. A., Murphy, A. B., Logothetis, C. J., Kim, J., Neuhausen, S. L., Steele, L., Ding, Y. C., Isaacs, W. B., Nemesure, B., Hennis, A. J. M., Carpten, J., Pandha, H., Michael, A., De Ruyck, K., De Meerleer, G., Ost, P., Xu, J., Razack, A., Lim, J., Teo, S. H., Newcomb, L. F., Lin, D. W., Fowke, J. H., Neslund-Dudas, C., Rybicki, B. A., Gamulin, M., Lessel, D., Kulis, T., Usmani, N., Singhal, S., Parliament, M., Claessens, F., Joniau, S., Van den Broeck, T., Gago-Dominguez, M., Castelao, J. E., Martinez, M. E., Larkin, S., Townsend, P. A., Aukim-Hastie, C., Bush, W. S., Aldrich, M. C., Crawford, D. C., Srivastava, S., Cullen, J. C., Petrovics, G., Casey, G., Roobol, M. J., Jenster, G., van Schaik, R. H. N., Hu, J. J., Sanderson, M., Varma, R., McKean-Cowdin, R., Torres, M., Mancuso, N., Berndt, S. I., Van Den Eeden, S. K., Easton, D. F., Chanock, S. J., Cook, M. B., Wiklund, F., Nakagawa, H., Witte, J. S., Eeles, R. A., Kote-Jarai, Z. & Haiman, C. A., Mar 2021, In: Nature Genetics. 53, 3, p. 413 1 p.

      Research output: Contribution to journal › Comment/debate › peer-review

      Open Access
      4 Scopus citations

    • Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study

      PRACTICAL consortium, Aug 1 2021, In: European Urology Oncology. 4, 4, p. 570-579 10 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      32 Scopus citations

    • Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

      Conti, D. V., Darst, B. F., Moss, L. C., Saunders, E. J., Sheng, X., Chou, A., Schumacher, F. R., Olama, A. A. A., Benlloch, S., Dadaev, T., Brook, M. N., Sahimi, A., Hoffmann, T. J., Takahashi, A., Matsuda, K., Momozawa, Y., Fujita, M., Muir, K., Lophatananon, A., Wan, P., & 211 othersLe Marchand, L., Wilkens, L. R., Stevens, V. L., Gapstur, S. M., Carter, B. D., Schleutker, J., Tammela, T. L. J., Sipeky, C., Auvinen, A., Giles, G. G., Southey, M. C., MacInnis, R. J., Cybulski, C., Wokołorczyk, D., Lubiński, J., Neal, D. E., Donovan, J. L., Hamdy, F. C., Martin, R. M., Nordestgaard, B. G., Nielsen, S. F., Weischer, M., Bojesen, S. E., Røder, M. A., Iversen, P., Batra, J., Chambers, S., Moya, L., Horvath, L., Clements, J. A., Tilley, W., Risbridger, G. P., Gronberg, H., Aly, M., Szulkin, R., Eklund, M., Nordström, T., Pashayan, N., Dunning, A. M., Ghoussaini, M., Travis, R. C., Key, T. J., Riboli, E., Park, J. Y., Sellers, T. A., Lin, H. Y., Albanes, D., Weinstein, S. J., Mucci, L. A., Giovannucci, E., Lindstrom, S., Kraft, P., Hunter, D. J., Penney, K. L., Turman, C., Tangen, C. M., Goodman, P. J., Thompson, I. M., Hamilton, R. J., Fleshner, N. E., Finelli, A., Parent, M. É., Stanford, J. L., Ostrander, E. A., Geybels, M. S., Koutros, S., Freeman, L. E. B., Stampfer, M., Wolk, A., Håkansson, N., Andriole, G. L., Hoover, R. N., Machiela, M. J., Sørensen, K. D., Borre, M., Blot, W. J., Zheng, W., Yeboah, E. D., Mensah, J. E., Lu, Y. J., Zhang, H. W., Feng, N., Mao, X., Wu, Y., Zhao, S. C., Sun, Z., Thibodeau, S. N., McDonnell, S. K., Schaid, D. J., West, C. M. L., Burnet, N., Barnett, G., Maier, C., Schnoeller, T., Luedeke, M., Kibel, A. S., Drake, B. F., Cussenot, O., Cancel-Tassin, G., Menegaux, F., Truong, T., Koudou, Y. A., John, E. M., Grindedal, E. M., Maehle, L., Khaw, K. T., Ingles, S. A., Stern, M. C., Vega, A., Gómez-Caamaño, A., Fachal, L., Rosenstein, B. S., Kerns, S. L., Ostrer, H., Teixeira, M. R., Paulo, P., Brandão, A., Watya, S., Lubwama, A., Bensen, J. T., Fontham, E. T. H., Mohler, J., Taylor, J. A., Kogevinas, M., Llorca, J., Castaño-Vinyals, G., Cannon-Albright, L., Teerlink, C. C., Huff, C. D., Strom, S. S., Multigner, L., Blanchet, P., Brureau, L., Kaneva, R., Slavov, C., Mitev, V., Leach, R. J., Weaver, B., Brenner, H., Cuk, K., Holleczek, B., Saum, K. U., Klein, E. A., Hsing, A. W., Kittles, R. A., Murphy, A. B., Logothetis, C. J., Kim, J., Neuhausen, S. L., Steele, L., Ding, Y. C., Isaacs, W. B., Nemesure, B., Hennis, A. J. M., Carpten, J., Pandha, H., Michael, A., De Ruyck, K., De Meerleer, G., Ost, P., Xu, J., Razack, A., Lim, J., Teo, S. H., Newcomb, L. F., Lin, D. W., Fowke, J. H., Neslund-Dudas, C., Rybicki, B. A., Gamulin, M., Lessel, D., Kulis, T., Usmani, N., Singhal, S., Parliament, M., Claessens, F., Joniau, S., Van den Broeck, T., Gago-Dominguez, M., Castelao, J. E., Martinez, M. E., Larkin, S., Townsend, P. A., Aukim-Hastie, C., Bush, W. S., Aldrich, M. C., Crawford, D. C., Srivastava, S., Cullen, J. C., Petrovics, G., Casey, G., Roobol, M. J., Jenster, G., van Schaik, R. H. N., Hu, J. J., Sanderson, M., Varma, R., McKean-Cowdin, R., Torres, M., Mancuso, N., Berndt, S. I., Van Den Eeden, S. K., Easton, D. F., Chanock, S. J., Cook, M. B., Wiklund, F., Nakagawa, H., Witte, J. S., Eeles, R. A., Kote-Jarai, Z. & Haiman, C. A., Jan 2021, In: Nature Genetics. 53, 1, p. 65-75 11 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      204 Scopus citations
    • 2020

      A genome-wide association study of prostate cancer in Latinos

      Du, Z., Hopp, H., Ingles, S. A., Huff, C., Sheng, X., Weaver, B., Stern, M., Hoffmann, T. J., John, E. M., Van Den Eeden, S. K., Strom, S., Leach, R. J., Thompson, I. M., Witte, J. S., Conti, D. V. & Haiman, C. A., Apr 1 2020, In: International journal of cancer. 146, 7, p. 1819-1826 8 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      23 Scopus citations

    • A Germline Variant at 8q24 Contributes to Familial Clustering of Prostate Cancer in Men of African Ancestry

      Darst, B. F., Wan, P., Sheng, X., Bensen, J. T., Ingles, S. A., Rybicki, B. A., Nemesure, B., John, E. M., Fowke, J. H., Stevens, V. L., Berndt, S. I., Huff, C. D., Strom, S. S., Park, J. Y., Zheng, W., Ostrander, E. A., Walsh, P. C., Srivastava, S., Carpten, J., Sellers, T. A., & 52 othersYamoah, K., Murphy, A. B., Sanderson, M., Crawford, D. C., Gapstur, S. M., Bush, W. S., Aldrich, M. C., Cussenot, O., Yeager, M., Petrovics, G., Cullen, J., Neslund-Dudas, C., Kittles, R. A., Xu, J., Stern, M. C., Kote-Jarai, Z., Govindasami, K., Chokkalingam, A. P., Multigner, L., Parent, M. E., Menegaux, F., Cancel-Tassin, G., Kibel, A. S., Klein, E. A., Goodman, P. J., Drake, B. F., Hu, J. J., Clark, P. E., Blanchet, P., Casey, G., Hennis, A. J. M., Lubwama, A., Thompson, I. M., Leach, R., Gundell, S. M., Pooler, L., Xia, L., Mohler, J. L., Fontham, E. T. H., Smith, G. J., Taylor, J. A., Eeles, R. A., Brureau, L., Chanock, S. J., Watya, S., Stanford, J. L., Mandal, D., Isaacs, W. B., Cooney, K., Blot, W. J., Conti, D. V. & Haiman, C. A., Sep 2020, In: European urology. 78, 3, p. 316-320 5 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      29 Scopus citations

    • A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposis

      Thompson, B. A., Snow, A. K., Koptiuch, C., Kohlmann, W. K., Mooney, R., Johnson, S., Huff, C. D., Yu, Y., Teerlink, C. C., Feng, B. J., Neklason, D. W., Cannon-Albright, L. A. & Tavtigian, S. V., Jun 1 2020, In: Clinical Genetics. 97, 6, p. 943-944 2 p.

      Research output: Contribution to journal › Letter › peer-review

      Open Access
      13 Scopus citations

    • Author Correction: Personalized Risk Assessment in Never, Light, and Heavy Smokers in a prospective cohort in Taiwan (Scientific Reports, (2016), 6, 1, (36482), 10.1038/srep36482)

      Wu, X., Wen, C. P., Ye, Y., Tsai, M. K., Wen, C., Roth, J. A., Pu, X., Chow, W. H., Huff, C., Cunningham, S., Huang, M., Wu, S., Tsao, C. K., Gu, J. & Lippman, S. M., Dec 1 2020, In: Scientific reports. 10, 1, 5514.

      Research output: Contribution to journal › Comment/debate › peer-review

      Open Access

    • Large-scale analysis of acquired chromosomal alterations in non-tumor samples from patients with cancer

      Jakubek, Y. A., Chang, K., Sivakumar, S., Yu, Y., Giordano, M. R., Fowler, J., Huff, C. D., Kadara, H., Vilar, E. & Scheet, P., Jan 1 2020, In: Nature biotechnology. 38, 1, p. 90-96 7 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      26 Scopus citations
    • 2019

      ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder

      Williams, L. B., Javed, A., Sabri, A., Morgan, D. J., Huff, C. D., Grigg, J. R., Heng, X. T., Khng, A. J., Hollink, I. H. I. M., Morrison, M. A., Owen, L. A., Anderson, K., Kinard, K., Greenlees, R., Novacic, D., Nida Sen, H., Zein, W. M., Rodgers, G. M., Vitale, A. T., Haider, N. B., & 21 othersHillmer, A. M., Ng, P. C., Shankaracharya, Cheng, A., Zheng, L., Gillies, M. C., van Slegtenhorst, M., van Hagen, P. M., Missotten, T. O. A. R., Farley, G. L., Polo, M., Malatack, J., Curtin, J., Martin, F., Arbuckle, S., Alexander, S. I., Chircop, M., Davila, S., Digre, K. B., Jamieson, R. V. & DeAngelis, M. M., Sep 1 2019, In: Genetics in Medicine. 21, 9, p. 2103-2115 13 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      28 Scopus citations

    • Assessing the performance of in silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancer

      Voskanian, A., Katsonis, P., Lichtarge, O., Pejaver, V., Radivojac, P., Mooney, S. D., Capriotti, E., Bromberg, Y., Wang, Y., Miller, M., Martelli, P. L., Savojardo, C., Babbi, G., Casadio, R., Cao, Y., Sun, Y., Shen, Y., Garg, A., Pal, D., Yu, Y., & 9 othersHuff, C. D., Tavtigian, S. V., Young, E., Neuhausen, S. L., Ziv, E., Pal, L. R., Andreoletti, G., Brenner, S. E. & Kann, M. G., Sep 1 2019, In: Human mutation. 40, 9, p. 1612-1622 11 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      6 Scopus citations

    • Association between Birth Defects and Cancer Risk among Children and Adolescents in a Population-Based Assessment of 10 Million Live Births

      Lupo, P. J., Schraw, J. M., Desrosiers, T. A., Nembhard, W. N., Langlois, P. H., Canfield, M. A., Copeland, G., Meyer, R. E., Brown, A. L., Chambers, T. M., Sok, P., Danysh, H. E., Carozza, S. E., Sisoudiya, S. D., Hilsenbeck, S. G., Janitz, A. E., Oster, M. E., Scheuerle, A. E., Schiffman, J. D., Luo, C., & 6 othersMian, A., Mueller, B. A., Huff, C. D., Rasmussen, S. A., Scheurer, M. E. & Plon, S. E., Aug 2019, In: JAMA Oncology. 5, 8, p. 1150-1158 9 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      84 Scopus citations

    • DNA Sequencing of Small Bowel Adenocarcinomas Identifies Targetable Recurrent Mutations in the ERBB2 Signaling Pathway

      Adam, L., San Lucas, F. A., Fowler, R., Yu, Y., Wu, W., Liu, Y., Wang, H., Menter, D., Tetzlaff, M. T., Ensor, J., Manyam, G., Arold, S. T., Huff, C., Kopetz, S., Scheet, P. & Overman, M. J., Jan 15 2019, In: Clinical cancer research : an official journal of the American Association for Cancer Research. 25, 2, p. 641-651 11 p.

      Research output: Contribution to journal › Article › peer-review

      21 Scopus citations

    • Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample

      Petty, L. E., Highland, H. M., Gamazon, E. R., Hu, H., Karhade, M., Chen, H. H., De Vries, P. S., Grove, M. L., Aguilar, D., Bell, G. I., Huff, C. D., Hanis, C. L., Doddapaneni, H., Munzy, D. M., Gibbs, R. A., Ma, J., Parra, E. J., Cruz, M., Valladares-Salgado, A., Arking, D. E., & 5 othersBarbeira, A., Im, H. K., Morrison, A. C., Boerwinkle, E. & Below, J. E., Apr 1 2019, In: Human molecular genetics. 28, 7, p. 1212-1224 13 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      10 Scopus citations

    • Tbx3-Mediated Regulation of Cardiac Conduction System Development and Function: Potential Contributions of Alternative RNA Processing

      Delisle, B. P., Yu, Y., Puvvula, P., Hall, A. R., Huff, C. & Moon, A. M., Oct 1 2019, In: Pediatric Cardiology. 40, 7, p. 1388-1400 13 p.

      Research output: Contribution to journal › Article › peer-review

    • 2018

      A Nonsynonymous Variant in the GOLM1 Gene in Cutaneous Malignant Melanoma

      Teerlink, C. C., Huff, C., Stevens, J., Yu, Y., Holmen, S. L., Silvis, M. R., Trombetti, K., Zhao, H., Grossman, D., Farnham, J. M., Wen, J., Facelli, J. C., Thomas, A., Babst, M., Florell, S. R., Meyer, L., Zone, J. J., Leachman, S. & Cannon-Albright, L. A., Dec 1 2018, In: Journal of the National Cancer Institute. 110, 12, p. 1380-1385 6 p.

      Research output: Contribution to journal › Article › peer-review

      27 Scopus citations

    • DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency

      SGP Consortium, Dec 6 2018, In: American journal of human genetics. 103, 6, p. 1038-1044 7 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      64 Scopus citations

    • Integrated case-control and somatic-germline interaction analyses of melanoma susceptibility genes

      Yu, Y., Hu, H., Chen, J. S., Hu, F., Fowler, J., Scheet, P., Zhao, H. & Huff, C. D., Jun 2018, In: Biochimica et Biophysica Acta - Molecular Basis of Disease. 1864, 6, p. 2247-2254 8 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      11 Scopus citations

    • Introgression of regulatory alleles and a missense coding mutation drive plumage pattern diversity in the rock pigeon

      Vickrey, A. I., Bruders, R., Kronenberg, Z., Mackey, E., Bohlender, R. J., Maclary, E. T., Maynez, R., Osborne, E. J., Johnson, K. P., Huff, C. D., Yandell, M. & Shapiro, M. D., Jul 17 2018, In: eLife. 7, e34803.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      48 Scopus citations

    • Targeted gene sequencing in children with Crohn's disease and their parents: Implications for missing heritability

      Chen, J. S., Hu, F., Kugathasan, S., Jorde, L. B., Nix, D., Rutherford, A., Denson, L., Watkins, S. W., Prahalad, S., Huff, C. & Guthery, S. L., Sep 1 2018, In: G3: Genes, Genomes, Genetics. 8, 9, p. 2881-2888 8 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      1 Scopus citations

    • The somatic mutation landscape of premalignant colorectal adenoma

      Lin, S. H., Raju, G. S., Huff, C., Ye, Y., Gu, J., Chen, J. S., Hildebrandt, M. A. T., Liang, H., Menter, D. G., Morris, J., Hawk, E., Stroehlein, J. R., Futreal, A., Kopetz, S., Mishra, L. & Wu, X., 2018, In: Gut. 67, 7, p. 1299-1305 7 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      46 Scopus citations

    • The VAAST Variant Prioritizer (VVP): Ultrafast, easy to use whole genome variant prioritization tool

      Flygare, S., Hernandez, E. J., Phan, L., Moore, B., Li, M., Fejes, A., Hu, H., Eilbeck, K., Huff, C., Jorde, L., G. Reese, M. & Yandell, M., Feb 20 2018, In: BMC bioinformatics. 19, 1, 57.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      21 Scopus citations

    • XPAT: a toolkit to conduct cross-platform association studies with heterogeneous sequencing datasets

      Yu, Y., Hu, H., Bohlender, R. J., Hu, F., Chen, J. S., Holt, C., Fowler, J., Guthery, S. L., Scheet, P., Hildebrandt, M. A. T., Yandell, M. & Huff, C. D., Apr 6 2018, In: Nucleic acids research. 46, 6, p. E32

      Research output: Contribution to journal › Article › peer-review

      Open Access
      5 Scopus citations
    • 2017

      Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African ancestry anthropometry genetics consortium

      The Bone Mineral Density in Childhood Study (BMDCS) Group, Apr 2017, In: PLoS genetics. 13, 4, e1006719.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      76 Scopus citations

    • Early history of Neanderthals and Denisovans

      Rogers, A. R., Bohlender, R. J. & Huff, C. D., Sep 12 2017, In: Proceedings of the National Academy of Sciences of the United States of America. 114, 37, p. 9859-9863 5 p.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      55 Scopus citations

    • Evolutionary history of Tibetans inferred from whole-genome sequencing

      Hu, H., Petousi, N., Glusman, G., Yu, Y., Bohlender, R. J., Tashi, T., Downie, J. M., Roach, J. C., Cole, A. M., Lorenzo, F. R., Rogers, A. R., Brunkow, M. E., Cavalleri, G., Hood, L., Alpatty, S. M., Prchal, J. T., Jorde, L. B., Robbins, P. A., Simonson, T. S. & Huff, C. D., Apr 2017, In: PLoS genetics. 13, 4, e1006675.

      Research output: Contribution to journal › Article › peer-review

      Open Access
      73 Scopus citations