1q21.1 deletion syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "1q21.1 deletion syndrome" in English language version.

refsWebsite

Global rank English rank

22nih.gov

4^th place

11doi.org

2^nd place

3worldcat.org

5^th place

2handle.net

102^nd place

76^th place

1medlineplus.gov

1,581^st place

1,299^th place

1web.archive.org

1^st place

1harvard.edu

18^th place

17^th place

1unige.ch

6,897^th place

6,705^th place

1semanticscholar.org

11^th place

8^th place

doi.org

Gillentine, M.A.; Lupo, P.J.; Stankiewicz, P.; Schaaf, C.P. (July 2008). "An estimation of the prevalence of genomic disorders using chromosomal microarray data". Journal of Human Genetics. 63 (7): 795–801. doi:10.1038/s10038-018-0451-x. ISSN 1434-5161. PMC 6019170. PMID 29691480.
Chen, Mei-Jou; Wei, Shin-Yi; Yang, Wei-Shiung; Wu, Tsai-Tzu; Li, Huei-Ying; Ho, Hong-Nerng; Yang, Yu-Shih; Chen, Pei-Lung (July 2015). "Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome". Human Reproduction (Oxford, England). 30 (7): 1732–1742. doi:10.1093/humrep/dev095. ISSN 1460-2350. PMID 25924657.
Stefansson, Hreinn; Rujescu, Dan; Cichon, Sven; Pietiläinen, Olli P. H.; Ingason, Andres; Steinberg, Stacy; Fossdal, Ragnheidur; Sigurdsson, Engilbert; Sigmundsson, Thordur; Buizer-Voskamp, Jacobine E.; Hansen, Thomas; Jakobsen, Klaus D.; Muglia, Pierandrea; Francks, Clyde; Matthews, Paul M.; Gylfason, Arnaldur; Halldorsson, Bjarni V.; Gudbjartsson, Daniel; Thorgeirsson, Thorgeir E.; Sigurdsson, Asgeir; Jonasdottir, Adalbjorg; Jonasdottir, Aslaug; Bjornsson, Asgeir; Mattiasdottir, Sigurborg; Blondal, Thorarinn; Haraldsson, Magnus; Magnusdottir, Brynja B.; Giegling, Ina; Möller, Hans-Jürgen; Hartmann, Annette; Shianna, Kevin V.; Ge, Dongliang; Need, Anna C.; Crombie, Caroline; Fraser, Gillian; Walker, Nicholas; Lonnqvist, Jouko; Suvisaari, Jaana; Tuulio-Henriksson, Annamarie; Paunio, Tiina; Toulopoulou, Timi; Bramon, Elvira; Di Forti, Marta; Murray, Robin; Ruggeri, Mirella; Vassos, Evangelos; Tosato, Sarah; Walshe, Muriel; Li, Tao; Vasilescu, Catalina; Mühleisen, Thomas W.; Wang, August G.; Ullum, Henrik; Djurovic, Srdjan; Melle, Ingrid; Olesen, Jes; Kiemeney, Lambertus A.; Franke, Barbara; Sabatti, Chiara; Freimer, Nelson B.; Gulcher, Jeffrey R.; Thorsteinsdottir, Unnur; Kong, Augustine; Andreassen, Ole A.; Ophoff, Roel A.; Georgi, Alexander; Rietschel, Marcella; Werge, Thomas; Petursson, Hannes; Goldstein, David B.; Nöthen, Markus M.; Peltonen, Leena; Collier, David A.; St Clair, David; Stefansson, Kari (September 2008). "Large recurrent microdeletions associated with schizophrenia". Nature. 455 (7210): 232–236. Bibcode:2008Natur.455..232S. doi:10.1038/nature07229. hdl:11858/00-001M-0000-0012-C93F-6. ISSN 1476-4687. PMC 2687075. PMID 18668039.
Mefford HC, Sharp AJ, Baker C, et al. (October 2008). "Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes". N. Engl. J. Med. 359 (16): 1685–99. doi:10.1056/NEJMoa0805384. hdl:2066/71235. PMC 2703742. PMID 18784092.
Levinson DF, Duan J, Oh S, et al. (March 2011). "Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications". Am J Psychiatry. 168 (3): 302–16. doi:10.1176/appi.ajp.2010.10060876. PMC 4441324. PMID 21285140.
Ikeda M, Aleksic B, Kirov G, et al. (February 2010). "Copy number variation in schizophrenia in the Japanese population". Biol. Psychiatry. 67 (3): 283–6. doi:10.1016/j.biopsych.2009.08.034. PMID 19880096. S2CID 26047827.
Li J, Zhou G, Ji W, et al. (March 2011). "Common variants in the BCL9 gene conferring risk of schizophrenia". Arch. Gen. Psychiatry. 68 (3): 232–40. doi:10.1001/archgenpsychiatry.2011.1. PMID 21383261.
e.g.: Dumas L, Sikela JM (2009). "DUF1220 domains, cognitive disease, and human brain evolution". Cold Spring Harb. Symp. Quant. Biol. 74: 375–82. doi:10.1101/sqb.2009.74.025. PMC 2902282. PMID 19850849.
Doggett NA, Xie G, Meincke LJ, et al. (Dec 2006). "A 360-kb interchromosomal duplication of the human HYDIN locus". Genomics. 88 (6): 762–71. doi:10.1016/j.ygeno.2006.07.012. PMID 16938426.
Harvard C (2011). "Understanding the impact of 1q21.1 copy number variant". Orphanet Journal of Rare Diseases. 6: 54. doi:10.1186/1750-1172-6-54. PMC 3180300. PMID 21824431.
Soemedi, R.; et al. (2011). "DPhenotype-Specific Effect of Chromosome 1q21.1 Rearrangements and GJA5 Duplications in 2436 Congenital Heart Disease Patients and 6760 Controls". Hum. Mol. Genet. 21 (7): 1513–1520. doi:10.1093/hmg/ddr589. PMC 3298277. PMID 22199024.

handle.net

hdl.handle.net

Stefansson, Hreinn; Rujescu, Dan; Cichon, Sven; Pietiläinen, Olli P. H.; Ingason, Andres; Steinberg, Stacy; Fossdal, Ragnheidur; Sigurdsson, Engilbert; Sigmundsson, Thordur; Buizer-Voskamp, Jacobine E.; Hansen, Thomas; Jakobsen, Klaus D.; Muglia, Pierandrea; Francks, Clyde; Matthews, Paul M.; Gylfason, Arnaldur; Halldorsson, Bjarni V.; Gudbjartsson, Daniel; Thorgeirsson, Thorgeir E.; Sigurdsson, Asgeir; Jonasdottir, Adalbjorg; Jonasdottir, Aslaug; Bjornsson, Asgeir; Mattiasdottir, Sigurborg; Blondal, Thorarinn; Haraldsson, Magnus; Magnusdottir, Brynja B.; Giegling, Ina; Möller, Hans-Jürgen; Hartmann, Annette; Shianna, Kevin V.; Ge, Dongliang; Need, Anna C.; Crombie, Caroline; Fraser, Gillian; Walker, Nicholas; Lonnqvist, Jouko; Suvisaari, Jaana; Tuulio-Henriksson, Annamarie; Paunio, Tiina; Toulopoulou, Timi; Bramon, Elvira; Di Forti, Marta; Murray, Robin; Ruggeri, Mirella; Vassos, Evangelos; Tosato, Sarah; Walshe, Muriel; Li, Tao; Vasilescu, Catalina; Mühleisen, Thomas W.; Wang, August G.; Ullum, Henrik; Djurovic, Srdjan; Melle, Ingrid; Olesen, Jes; Kiemeney, Lambertus A.; Franke, Barbara; Sabatti, Chiara; Freimer, Nelson B.; Gulcher, Jeffrey R.; Thorsteinsdottir, Unnur; Kong, Augustine; Andreassen, Ole A.; Ophoff, Roel A.; Georgi, Alexander; Rietschel, Marcella; Werge, Thomas; Petursson, Hannes; Goldstein, David B.; Nöthen, Markus M.; Peltonen, Leena; Collier, David A.; St Clair, David; Stefansson, Kari (September 2008). "Large recurrent microdeletions associated with schizophrenia". Nature. 455 (7210): 232–236. Bibcode:2008Natur.455..232S. doi:10.1038/nature07229. hdl:11858/00-001M-0000-0012-C93F-6. ISSN 1476-4687. PMC 2687075. PMID 18668039.
Mefford HC, Sharp AJ, Baker C, et al. (October 2008). "Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes". N. Engl. J. Med. 359 (16): 1685–99. doi:10.1056/NEJMoa0805384. hdl:2066/71235. PMC 2703742. PMID 18784092.

harvard.edu

ui.adsabs.harvard.edu

Stefansson, Hreinn; Rujescu, Dan; Cichon, Sven; Pietiläinen, Olli P. H.; Ingason, Andres; Steinberg, Stacy; Fossdal, Ragnheidur; Sigurdsson, Engilbert; Sigmundsson, Thordur; Buizer-Voskamp, Jacobine E.; Hansen, Thomas; Jakobsen, Klaus D.; Muglia, Pierandrea; Francks, Clyde; Matthews, Paul M.; Gylfason, Arnaldur; Halldorsson, Bjarni V.; Gudbjartsson, Daniel; Thorgeirsson, Thorgeir E.; Sigurdsson, Asgeir; Jonasdottir, Adalbjorg; Jonasdottir, Aslaug; Bjornsson, Asgeir; Mattiasdottir, Sigurborg; Blondal, Thorarinn; Haraldsson, Magnus; Magnusdottir, Brynja B.; Giegling, Ina; Möller, Hans-Jürgen; Hartmann, Annette; Shianna, Kevin V.; Ge, Dongliang; Need, Anna C.; Crombie, Caroline; Fraser, Gillian; Walker, Nicholas; Lonnqvist, Jouko; Suvisaari, Jaana; Tuulio-Henriksson, Annamarie; Paunio, Tiina; Toulopoulou, Timi; Bramon, Elvira; Di Forti, Marta; Murray, Robin; Ruggeri, Mirella; Vassos, Evangelos; Tosato, Sarah; Walshe, Muriel; Li, Tao; Vasilescu, Catalina; Mühleisen, Thomas W.; Wang, August G.; Ullum, Henrik; Djurovic, Srdjan; Melle, Ingrid; Olesen, Jes; Kiemeney, Lambertus A.; Franke, Barbara; Sabatti, Chiara; Freimer, Nelson B.; Gulcher, Jeffrey R.; Thorsteinsdottir, Unnur; Kong, Augustine; Andreassen, Ole A.; Ophoff, Roel A.; Georgi, Alexander; Rietschel, Marcella; Werge, Thomas; Petursson, Hannes; Goldstein, David B.; Nöthen, Markus M.; Peltonen, Leena; Collier, David A.; St Clair, David; Stefansson, Kari (September 2008). "Large recurrent microdeletions associated with schizophrenia". Nature. 455 (7210): 232–236. Bibcode:2008Natur.455..232S. doi:10.1038/nature07229. hdl:11858/00-001M-0000-0012-C93F-6. ISSN 1476-4687. PMC 2687075. PMID 18668039.

medlineplus.gov

"1q21.1 microdeletion: MedlinePlus Genetics". medlineplus.gov. Retrieved 2023-07-25.

nih.gov

pubmed.ncbi.nlm.nih.gov

Haldeman-Englert, Chad R.; Jewett, Tamison (24 February 2011). "1q21.1 Recurrent Deletion". 1q21.1 Recurrent Microdeletion. Seattle (WA): University of Washington, Seattle. PMID 21348049 – via PubMed.
Gillentine, M.A.; Lupo, P.J.; Stankiewicz, P.; Schaaf, C.P. (July 2008). "An estimation of the prevalence of genomic disorders using chromosomal microarray data". Journal of Human Genetics. 63 (7): 795–801. doi:10.1038/s10038-018-0451-x. ISSN 1434-5161. PMC 6019170. PMID 29691480.
Chen, Mei-Jou; Wei, Shin-Yi; Yang, Wei-Shiung; Wu, Tsai-Tzu; Li, Huei-Ying; Ho, Hong-Nerng; Yang, Yu-Shih; Chen, Pei-Lung (July 2015). "Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome". Human Reproduction (Oxford, England). 30 (7): 1732–1742. doi:10.1093/humrep/dev095. ISSN 1460-2350. PMID 25924657.
Stefansson, Hreinn; Rujescu, Dan; Cichon, Sven; Pietiläinen, Olli P. H.; Ingason, Andres; Steinberg, Stacy; Fossdal, Ragnheidur; Sigurdsson, Engilbert; Sigmundsson, Thordur; Buizer-Voskamp, Jacobine E.; Hansen, Thomas; Jakobsen, Klaus D.; Muglia, Pierandrea; Francks, Clyde; Matthews, Paul M.; Gylfason, Arnaldur; Halldorsson, Bjarni V.; Gudbjartsson, Daniel; Thorgeirsson, Thorgeir E.; Sigurdsson, Asgeir; Jonasdottir, Adalbjorg; Jonasdottir, Aslaug; Bjornsson, Asgeir; Mattiasdottir, Sigurborg; Blondal, Thorarinn; Haraldsson, Magnus; Magnusdottir, Brynja B.; Giegling, Ina; Möller, Hans-Jürgen; Hartmann, Annette; Shianna, Kevin V.; Ge, Dongliang; Need, Anna C.; Crombie, Caroline; Fraser, Gillian; Walker, Nicholas; Lonnqvist, Jouko; Suvisaari, Jaana; Tuulio-Henriksson, Annamarie; Paunio, Tiina; Toulopoulou, Timi; Bramon, Elvira; Di Forti, Marta; Murray, Robin; Ruggeri, Mirella; Vassos, Evangelos; Tosato, Sarah; Walshe, Muriel; Li, Tao; Vasilescu, Catalina; Mühleisen, Thomas W.; Wang, August G.; Ullum, Henrik; Djurovic, Srdjan; Melle, Ingrid; Olesen, Jes; Kiemeney, Lambertus A.; Franke, Barbara; Sabatti, Chiara; Freimer, Nelson B.; Gulcher, Jeffrey R.; Thorsteinsdottir, Unnur; Kong, Augustine; Andreassen, Ole A.; Ophoff, Roel A.; Georgi, Alexander; Rietschel, Marcella; Werge, Thomas; Petursson, Hannes; Goldstein, David B.; Nöthen, Markus M.; Peltonen, Leena; Collier, David A.; St Clair, David; Stefansson, Kari (September 2008). "Large recurrent microdeletions associated with schizophrenia". Nature. 455 (7210): 232–236. Bibcode:2008Natur.455..232S. doi:10.1038/nature07229. hdl:11858/00-001M-0000-0012-C93F-6. ISSN 1476-4687. PMC 2687075. PMID 18668039.
Mefford HC, Sharp AJ, Baker C, et al. (October 2008). "Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes". N. Engl. J. Med. 359 (16): 1685–99. doi:10.1056/NEJMoa0805384. hdl:2066/71235. PMC 2703742. PMID 18784092.
Levinson DF, Duan J, Oh S, et al. (March 2011). "Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications". Am J Psychiatry. 168 (3): 302–16. doi:10.1176/appi.ajp.2010.10060876. PMC 4441324. PMID 21285140.
Ikeda M, Aleksic B, Kirov G, et al. (February 2010). "Copy number variation in schizophrenia in the Japanese population". Biol. Psychiatry. 67 (3): 283–6. doi:10.1016/j.biopsych.2009.08.034. PMID 19880096. S2CID 26047827.
Li J, Zhou G, Ji W, et al. (March 2011). "Common variants in the BCL9 gene conferring risk of schizophrenia". Arch. Gen. Psychiatry. 68 (3): 232–40. doi:10.1001/archgenpsychiatry.2011.1. PMID 21383261.
e.g.: Dumas L, Sikela JM (2009). "DUF1220 domains, cognitive disease, and human brain evolution". Cold Spring Harb. Symp. Quant. Biol. 74: 375–82. doi:10.1101/sqb.2009.74.025. PMC 2902282. PMID 19850849.
Doggett NA, Xie G, Meincke LJ, et al. (Dec 2006). "A 360-kb interchromosomal duplication of the human HYDIN locus". Genomics. 88 (6): 762–71. doi:10.1016/j.ygeno.2006.07.012. PMID 16938426.
Harvard C (2011). "Understanding the impact of 1q21.1 copy number variant". Orphanet Journal of Rare Diseases. 6: 54. doi:10.1186/1750-1172-6-54. PMC 3180300. PMID 21824431.
Soemedi, R.; et al. (2011). "DPhenotype-Specific Effect of Chromosome 1q21.1 Rearrangements and GJA5 Duplications in 2436 Congenital Heart Disease Patients and 6760 Controls". Hum. Mol. Genet. 21 (7): 1513–1520. doi:10.1093/hmg/ddr589. PMC 3298277. PMID 22199024.

ncbi.nlm.nih.gov

Haldeman-Englert, Chad R.; Jewett, Tamison (24 February 2011). "1q21.1 Recurrent Deletion". 1q21.1 Recurrent Microdeletion. Seattle (WA): University of Washington, Seattle. PMID 21348049 – via PubMed.
Gillentine, M.A.; Lupo, P.J.; Stankiewicz, P.; Schaaf, C.P. (July 2008). "An estimation of the prevalence of genomic disorders using chromosomal microarray data". Journal of Human Genetics. 63 (7): 795–801. doi:10.1038/s10038-018-0451-x. ISSN 1434-5161. PMC 6019170. PMID 29691480.
Stefansson, Hreinn; Rujescu, Dan; Cichon, Sven; Pietiläinen, Olli P. H.; Ingason, Andres; Steinberg, Stacy; Fossdal, Ragnheidur; Sigurdsson, Engilbert; Sigmundsson, Thordur; Buizer-Voskamp, Jacobine E.; Hansen, Thomas; Jakobsen, Klaus D.; Muglia, Pierandrea; Francks, Clyde; Matthews, Paul M.; Gylfason, Arnaldur; Halldorsson, Bjarni V.; Gudbjartsson, Daniel; Thorgeirsson, Thorgeir E.; Sigurdsson, Asgeir; Jonasdottir, Adalbjorg; Jonasdottir, Aslaug; Bjornsson, Asgeir; Mattiasdottir, Sigurborg; Blondal, Thorarinn; Haraldsson, Magnus; Magnusdottir, Brynja B.; Giegling, Ina; Möller, Hans-Jürgen; Hartmann, Annette; Shianna, Kevin V.; Ge, Dongliang; Need, Anna C.; Crombie, Caroline; Fraser, Gillian; Walker, Nicholas; Lonnqvist, Jouko; Suvisaari, Jaana; Tuulio-Henriksson, Annamarie; Paunio, Tiina; Toulopoulou, Timi; Bramon, Elvira; Di Forti, Marta; Murray, Robin; Ruggeri, Mirella; Vassos, Evangelos; Tosato, Sarah; Walshe, Muriel; Li, Tao; Vasilescu, Catalina; Mühleisen, Thomas W.; Wang, August G.; Ullum, Henrik; Djurovic, Srdjan; Melle, Ingrid; Olesen, Jes; Kiemeney, Lambertus A.; Franke, Barbara; Sabatti, Chiara; Freimer, Nelson B.; Gulcher, Jeffrey R.; Thorsteinsdottir, Unnur; Kong, Augustine; Andreassen, Ole A.; Ophoff, Roel A.; Georgi, Alexander; Rietschel, Marcella; Werge, Thomas; Petursson, Hannes; Goldstein, David B.; Nöthen, Markus M.; Peltonen, Leena; Collier, David A.; St Clair, David; Stefansson, Kari (September 2008). "Large recurrent microdeletions associated with schizophrenia". Nature. 455 (7210): 232–236. Bibcode:2008Natur.455..232S. doi:10.1038/nature07229. hdl:11858/00-001M-0000-0012-C93F-6. ISSN 1476-4687. PMC 2687075. PMID 18668039.
Mefford HC, Sharp AJ, Baker C, et al. (October 2008). "Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes". N. Engl. J. Med. 359 (16): 1685–99. doi:10.1056/NEJMoa0805384. hdl:2066/71235. PMC 2703742. PMID 18784092.
Levinson DF, Duan J, Oh S, et al. (March 2011). "Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications". Am J Psychiatry. 168 (3): 302–16. doi:10.1176/appi.ajp.2010.10060876. PMC 4441324. PMID 21285140.
e.g.: Dumas L, Sikela JM (2009). "DUF1220 domains, cognitive disease, and human brain evolution". Cold Spring Harb. Symp. Quant. Biol. 74: 375–82. doi:10.1101/sqb.2009.74.025. PMC 2902282. PMID 19850849.
Harvard C (2011). "Understanding the impact of 1q21.1 copy number variant". Orphanet Journal of Rare Diseases. 6: 54. doi:10.1186/1750-1172-6-54. PMC 3180300. PMID 21824431.
Soemedi, R.; et al. (2011). "DPhenotype-Specific Effect of Chromosome 1q21.1 Rearrangements and GJA5 Duplications in 2436 Congenital Heart Disease Patients and 6760 Controls". Hum. Mol. Genet. 21 (7): 1513–1520. doi:10.1093/hmg/ddr589. PMC 3298277. PMID 22199024.

rarediseases.info.nih.gov

"1q21.1 microdeletion syndrome — About the Disease — Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2023-07-25.
"Overview: 1q21.1 microdeletion syndrome". Genetic and Rare Diseases Information Center (GARD). Office of Rare Diseases Research • U.S. National Institutes of Health. 8 August 2011. Archived from the original on 2 June 2013. Retrieved 9 September 2013.

semanticscholar.org

api.semanticscholar.org

Ikeda M, Aleksic B, Kirov G, et al. (February 2010). "Copy number variation in schizophrenia in the Japanese population". Biol. Psychiatry. 67 (3): 283–6. doi:10.1016/j.biopsych.2009.08.034. PMID 19880096. S2CID 26047827.

unige.ch

archive-ouverte.unige.ch

Mefford HC, Sharp AJ, Baker C, et al. (October 2008). "Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes". N. Engl. J. Med. 359 (16): 1685–99. doi:10.1056/NEJMoa0805384. hdl:2066/71235. PMC 2703742. PMID 18784092.

web.archive.org

"Overview: 1q21.1 microdeletion syndrome". Genetic and Rare Diseases Information Center (GARD). Office of Rare Diseases Research • U.S. National Institutes of Health. 8 August 2011. Archived from the original on 2 June 2013. Retrieved 9 September 2013.

worldcat.org

search.worldcat.org

Gillentine, M.A.; Lupo, P.J.; Stankiewicz, P.; Schaaf, C.P. (July 2008). "An estimation of the prevalence of genomic disorders using chromosomal microarray data". Journal of Human Genetics. 63 (7): 795–801. doi:10.1038/s10038-018-0451-x. ISSN 1434-5161. PMC 6019170. PMID 29691480.
Chen, Mei-Jou; Wei, Shin-Yi; Yang, Wei-Shiung; Wu, Tsai-Tzu; Li, Huei-Ying; Ho, Hong-Nerng; Yang, Yu-Shih; Chen, Pei-Lung (July 2015). "Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome". Human Reproduction (Oxford, England). 30 (7): 1732–1742. doi:10.1093/humrep/dev095. ISSN 1460-2350. PMID 25924657.
Stefansson, Hreinn; Rujescu, Dan; Cichon, Sven; Pietiläinen, Olli P. H.; Ingason, Andres; Steinberg, Stacy; Fossdal, Ragnheidur; Sigurdsson, Engilbert; Sigmundsson, Thordur; Buizer-Voskamp, Jacobine E.; Hansen, Thomas; Jakobsen, Klaus D.; Muglia, Pierandrea; Francks, Clyde; Matthews, Paul M.; Gylfason, Arnaldur; Halldorsson, Bjarni V.; Gudbjartsson, Daniel; Thorgeirsson, Thorgeir E.; Sigurdsson, Asgeir; Jonasdottir, Adalbjorg; Jonasdottir, Aslaug; Bjornsson, Asgeir; Mattiasdottir, Sigurborg; Blondal, Thorarinn; Haraldsson, Magnus; Magnusdottir, Brynja B.; Giegling, Ina; Möller, Hans-Jürgen; Hartmann, Annette; Shianna, Kevin V.; Ge, Dongliang; Need, Anna C.; Crombie, Caroline; Fraser, Gillian; Walker, Nicholas; Lonnqvist, Jouko; Suvisaari, Jaana; Tuulio-Henriksson, Annamarie; Paunio, Tiina; Toulopoulou, Timi; Bramon, Elvira; Di Forti, Marta; Murray, Robin; Ruggeri, Mirella; Vassos, Evangelos; Tosato, Sarah; Walshe, Muriel; Li, Tao; Vasilescu, Catalina; Mühleisen, Thomas W.; Wang, August G.; Ullum, Henrik; Djurovic, Srdjan; Melle, Ingrid; Olesen, Jes; Kiemeney, Lambertus A.; Franke, Barbara; Sabatti, Chiara; Freimer, Nelson B.; Gulcher, Jeffrey R.; Thorsteinsdottir, Unnur; Kong, Augustine; Andreassen, Ole A.; Ophoff, Roel A.; Georgi, Alexander; Rietschel, Marcella; Werge, Thomas; Petursson, Hannes; Goldstein, David B.; Nöthen, Markus M.; Peltonen, Leena; Collier, David A.; St Clair, David; Stefansson, Kari (September 2008). "Large recurrent microdeletions associated with schizophrenia". Nature. 455 (7210): 232–236. Bibcode:2008Natur.455..232S. doi:10.1038/nature07229. hdl:11858/00-001M-0000-0012-C93F-6. ISSN 1476-4687. PMC 2687075. PMID 18668039.