Exome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Exome" in English language version.

Last modified: 11:01:17, 11 August 2026 (UTC)

Ref.Un. Ref.Website

Global rank English rank

3026nih.gov

5^th place

1816doi.org

2^nd place

97adsabs.harvard.edu

14^th place

9^th place

22semanticscholar.org

15^th place

8^th place

22medlineplus.gov

1,521^st place

1,017^th place

adsabs.harvard.edu (Global: 14^th place; English: 9^th place)

ui.adsabs.harvard.edu

Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, Sutton GG, et al. (February 2001). "The sequence of the human genome". Science. 291 (5507): 1304–51. Bibcode:2001Sci...291.1304V. doi:10.1126/science.1058040. PMID 11181995.
Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, et al. (September 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–6. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, et al. (November 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proceedings of the National Academy of Sciences of the United States of America. 106 (45): 19096–101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545.
Erjavec SO, Gelfman S, Abdelaziz AR, Lee EY, Monga I, Alkelai A, Ionita-Laza I, Petukhova L, Christiano AM (Feb 2022). "Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82". Nat Commun. 13 (1) 800. Bibcode:2022NatCo..13..800E. doi:10.1038/s41467-022-28343-3. PMC 8831607. PMID 35145093.
Belkadi A, Bolze A, Itan Y, Cobat A, Vincent QB, Antipenko A, et al. (April 2015). "Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants". Proceedings of the National Academy of Sciences of the United States of America. 112 (17): 5473–8. Bibcode:2015PNAS..112.5473B. doi:10.1073/pnas.1418631112. PMC 4418901. PMID 25827230.
Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, et al. (September 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–6. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, et al. (November 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proceedings of the National Academy of Sciences of the United States of America. 106 (45): 19096–101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545.

doi.org (Global: 2^nd place; English: 2^nd place)

Bamshad MJ, Ng SB, Bigham AW, Tabor HK, Emond MJ, Nickerson DA, Shendure J (September 2011). "Exome sequencing as a tool for Mendelian disease gene discovery". Nature Reviews Genetics. 12 (11): 745–55. doi:10.1038/nrg3031. PMID 21946919. S2CID 15615317.
Sakharkar MK, Chow VT, Kangueane P (2004). "Distributions of exons and introns in the human genome". In Silico Biology. 4 (4): 387–93. doi:10.3233/ISB-00142. PMID 15217358.
Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, Sutton GG, et al. (February 2001). "The sequence of the human genome". Science. 291 (5507): 1304–51. Bibcode:2001Sci...291.1304V. doi:10.1126/science.1058040. PMID 11181995.
Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, et al. (September 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–6. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, et al. (November 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proceedings of the National Academy of Sciences of the United States of America. 106 (45): 19096–101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545.
Erjavec SO, Gelfman S, Abdelaziz AR, Lee EY, Monga I, Alkelai A, Ionita-Laza I, Petukhova L, Christiano AM (Feb 2022). "Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82". Nat Commun. 13 (1) 800. Bibcode:2022NatCo..13..800E. doi:10.1038/s41467-022-28343-3. PMC 8831607. PMID 35145093.
Yang Y, Muzny DM, Reid JG, Bainbridge MN, Willis A, Ward PA, et al. (October 2013). "Clinical whole-exome sequencing for the diagnosis of mendelian disorders". The New England Journal of Medicine. 369 (16): 1502–11. doi:10.1056/NEJMoa1306555. PMC 4211433. PMID 24088041.
Nagele P (November 2013). "Exome sequencing: one small step for malignant hyperthermia, one giant step for our specialty—why exome sequencing matters to all of us, not just the experts". Anesthesiology. 119 (5): 1006–8. doi:10.1097/ALN.0b013e3182a8a90c. PMC 3980570. PMID 24195944.
Belkadi A, Bolze A, Itan Y, Cobat A, Vincent QB, Antipenko A, et al. (April 2015). "Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants". Proceedings of the National Academy of Sciences of the United States of America. 112 (17): 5473–8. Bibcode:2015PNAS..112.5473B. doi:10.1073/pnas.1418631112. PMC 4418901. PMID 25827230.
Gaff CL, Macciocca I (2016-01-01). "Chapter 15 – Genomic Perspective of Genetic Counseling". In Kumar D, Antonarakis S (eds.). Medical and Health Genomics. Academic Press. pp. 201–212. doi:10.1016/b978-0-12-420196-5.00015-0. ISBN 978-0-12-420196-5.
Zhu X, Petrovski S, Xie P, Ruzzo EK, Lu YF, McSweeney KM, et al. (October 2015). "Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios". Genetics in Medicine. 17 (10): 774–81. doi:10.1038/gim.2014.191. PMC 4791490. PMID 25590979.
Frésard L, Montgomery SB (December 2018). "Diagnosing rare diseases after the exome". Cold Spring Harbor Molecular Case Studies. 4 (6) a003392. doi:10.1101/mcs.a003392. PMC 6318767. PMID 30559314.
Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, et al. (September 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–6. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571.
Suleiman SH, Koko ME, Nasir WH, Elfateh O, Elgizouli UK, Abdallah MO, et al. (2015). "Exome sequencing of a colorectal cancer family reveals shared mutation pattern and predisposition circuitry along tumor pathways". Frontiers in Genetics. 6: 288. doi:10.3389/fgene.2015.00288. PMC 4584935. PMID 26442106.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, et al. (November 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proceedings of the National Academy of Sciences of the United States of America. 106 (45): 19096–101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545.
Bamshad MJ, Ng SB, Bigham AW, Tabor HK, Emond MJ, Nickerson DA, Shendure J (September 2011). "Exome sequencing as a tool for Mendelian disease gene discovery". Nature Reviews Genetics. 12 (11): 745–55. doi:10.1038/nrg3031. PMID 21946919. S2CID 15615317.

medlineplus.gov (Global: 1,521^st place; English: 1,017^th place)

"What are whole exome sequencing and whole genome sequencing?". Genetics Home Reference. National Library of Medicine, National Institutes of Health, U.S. Department of Health & Human Services. Retrieved 2019-11-07.
"Bartter syndrome". Genetics Home Reference. National Library of Medicine, National Institutes of Health, U.S. Department of Health & Human Services. Retrieved 2019-11-19.

nih.gov (Global: 5^th place; English: 5^th place)

pubmed.ncbi.nlm.nih.gov

Bamshad MJ, Ng SB, Bigham AW, Tabor HK, Emond MJ, Nickerson DA, Shendure J (September 2011). "Exome sequencing as a tool for Mendelian disease gene discovery". Nature Reviews Genetics. 12 (11): 745–55. doi:10.1038/nrg3031. PMID 21946919. S2CID 15615317.
Sakharkar MK, Chow VT, Kangueane P (2004). "Distributions of exons and introns in the human genome". In Silico Biology. 4 (4): 387–93. doi:10.3233/ISB-00142. PMID 15217358.
Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, Sutton GG, et al. (February 2001). "The sequence of the human genome". Science. 291 (5507): 1304–51. Bibcode:2001Sci...291.1304V. doi:10.1126/science.1058040. PMID 11181995.
Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, et al. (September 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–6. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, et al. (November 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proceedings of the National Academy of Sciences of the United States of America. 106 (45): 19096–101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545.
Erjavec SO, Gelfman S, Abdelaziz AR, Lee EY, Monga I, Alkelai A, Ionita-Laza I, Petukhova L, Christiano AM (Feb 2022). "Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82". Nat Commun. 13 (1) 800. Bibcode:2022NatCo..13..800E. doi:10.1038/s41467-022-28343-3. PMC 8831607. PMID 35145093.
Yang Y, Muzny DM, Reid JG, Bainbridge MN, Willis A, Ward PA, et al. (October 2013). "Clinical whole-exome sequencing for the diagnosis of mendelian disorders". The New England Journal of Medicine. 369 (16): 1502–11. doi:10.1056/NEJMoa1306555. PMC 4211433. PMID 24088041.
Nagele P (November 2013). "Exome sequencing: one small step for malignant hyperthermia, one giant step for our specialty—why exome sequencing matters to all of us, not just the experts". Anesthesiology. 119 (5): 1006–8. doi:10.1097/ALN.0b013e3182a8a90c. PMC 3980570. PMID 24195944.
Belkadi A, Bolze A, Itan Y, Cobat A, Vincent QB, Antipenko A, et al. (April 2015). "Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants". Proceedings of the National Academy of Sciences of the United States of America. 112 (17): 5473–8. Bibcode:2015PNAS..112.5473B. doi:10.1073/pnas.1418631112. PMC 4418901. PMID 25827230.
Zhu X, Petrovski S, Xie P, Ruzzo EK, Lu YF, McSweeney KM, et al. (October 2015). "Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios". Genetics in Medicine. 17 (10): 774–81. doi:10.1038/gim.2014.191. PMC 4791490. PMID 25590979.
Frésard L, Montgomery SB (December 2018). "Diagnosing rare diseases after the exome". Cold Spring Harbor Molecular Case Studies. 4 (6) a003392. doi:10.1101/mcs.a003392. PMC 6318767. PMID 30559314.
Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, et al. (September 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–6. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571.
Suleiman SH, Koko ME, Nasir WH, Elfateh O, Elgizouli UK, Abdallah MO, et al. (2015). "Exome sequencing of a colorectal cancer family reveals shared mutation pattern and predisposition circuitry along tumor pathways". Frontiers in Genetics. 6: 288. doi:10.3389/fgene.2015.00288. PMC 4584935. PMID 26442106.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, et al. (November 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proceedings of the National Academy of Sciences of the United States of America. 106 (45): 19096–101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545.
Bamshad MJ, Ng SB, Bigham AW, Tabor HK, Emond MJ, Nickerson DA, Shendure J (September 2011). "Exome sequencing as a tool for Mendelian disease gene discovery". Nature Reviews Genetics. 12 (11): 745–55. doi:10.1038/nrg3031. PMID 21946919. S2CID 15615317.

ncbi.nlm.nih.gov

Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, et al. (September 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–6. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, et al. (November 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proceedings of the National Academy of Sciences of the United States of America. 106 (45): 19096–101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545.
Erjavec SO, Gelfman S, Abdelaziz AR, Lee EY, Monga I, Alkelai A, Ionita-Laza I, Petukhova L, Christiano AM (Feb 2022). "Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82". Nat Commun. 13 (1) 800. Bibcode:2022NatCo..13..800E. doi:10.1038/s41467-022-28343-3. PMC 8831607. PMID 35145093.
Yang Y, Muzny DM, Reid JG, Bainbridge MN, Willis A, Ward PA, et al. (October 2013). "Clinical whole-exome sequencing for the diagnosis of mendelian disorders". The New England Journal of Medicine. 369 (16): 1502–11. doi:10.1056/NEJMoa1306555. PMC 4211433. PMID 24088041.
Nagele P (November 2013). "Exome sequencing: one small step for malignant hyperthermia, one giant step for our specialty—why exome sequencing matters to all of us, not just the experts". Anesthesiology. 119 (5): 1006–8. doi:10.1097/ALN.0b013e3182a8a90c. PMC 3980570. PMID 24195944.
Belkadi A, Bolze A, Itan Y, Cobat A, Vincent QB, Antipenko A, et al. (April 2015). "Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants". Proceedings of the National Academy of Sciences of the United States of America. 112 (17): 5473–8. Bibcode:2015PNAS..112.5473B. doi:10.1073/pnas.1418631112. PMC 4418901. PMID 25827230.
Zhu X, Petrovski S, Xie P, Ruzzo EK, Lu YF, McSweeney KM, et al. (October 2015). "Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios". Genetics in Medicine. 17 (10): 774–81. doi:10.1038/gim.2014.191. PMC 4791490. PMID 25590979.
Frésard L, Montgomery SB (December 2018). "Diagnosing rare diseases after the exome". Cold Spring Harbor Molecular Case Studies. 4 (6) a003392. doi:10.1101/mcs.a003392. PMC 6318767. PMID 30559314.
Ng SB, Turner EH, Robertson PD, Flygare SD, Bigham AW, Lee C, et al. (September 2009). "Targeted capture and massively parallel sequencing of 12 human exomes". Nature. 461 (7261): 272–6. Bibcode:2009Natur.461..272N. doi:10.1038/nature08250. PMC 2844771. PMID 19684571.
Suleiman SH, Koko ME, Nasir WH, Elfateh O, Elgizouli UK, Abdallah MO, et al. (2015). "Exome sequencing of a colorectal cancer family reveals shared mutation pattern and predisposition circuitry along tumor pathways". Frontiers in Genetics. 6: 288. doi:10.3389/fgene.2015.00288. PMC 4584935. PMID 26442106.
Choi M, Scholl UI, Ji W, Liu T, Tikhonova IR, Zumbo P, et al. (November 2009). "Genetic diagnosis by whole exome capture and massively parallel DNA sequencing". Proceedings of the National Academy of Sciences of the United States of America. 106 (45): 19096–101. Bibcode:2009PNAS..10619096C. doi:10.1073/pnas.0910672106. PMC 2768590. PMID 19861545.

semanticscholar.org (Global: 15^th place; English: 8^th place)

api.semanticscholar.org

Bamshad MJ, Ng SB, Bigham AW, Tabor HK, Emond MJ, Nickerson DA, Shendure J (September 2011). "Exome sequencing as a tool for Mendelian disease gene discovery". Nature Reviews Genetics. 12 (11): 745–55. doi:10.1038/nrg3031. PMID 21946919. S2CID 15615317.
Bamshad MJ, Ng SB, Bigham AW, Tabor HK, Emond MJ, Nickerson DA, Shendure J (September 2011). "Exome sequencing as a tool for Mendelian disease gene discovery". Nature Reviews Genetics. 12 (11): 745–55. doi:10.1038/nrg3031. PMID 21946919. S2CID 15615317.

Exome (English Wikipedia)

adsabs.harvard.edu (Global: 14th place; English: 9th place)

ui.adsabs.harvard.edu

doi.org (Global: 2nd place; English: 2nd place)

medlineplus.gov (Global: 1,521st place; English: 1,017th place)

nih.gov (Global: 5th place; English: 5th place)