Silver–Russell syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Silver–Russell syndrome" in English language version.

refsWebsite

Global rank English rank

17nih.gov

4^th place

12doi.org

2^nd place

6semanticscholar.org

11^th place

8^th place

6worldcat.org

5^th place

2web.archive.org

1^st place

2uzh.ch

3,633^rd place

3,091^st place

1patient.info

low place

7,180^th place

1omim.org

4,380^th place

4,305^th place

1nature.com

234^th place

397^th place

1birmingham.ac.uk

low place

7,843^rd place

1handle.net

102^nd place

76^th place

1childgrowthfoundation.org

low place

1whonamedit.com

2,888^th place

2,730^th place

birmingham.ac.uk

research.birmingham.ac.uk

Wakeling, Emma L.; Brioude, Frédéric; Lokulo-Sodipe, Oluwakemi; O'Connell, Susan M.; Salem, Jennifer; Bliek, Jet; Canton, Ana P. M.; Chrzanowska, Krystyna H.; Davies, Justin H. (2016-09-02). "Diagnosis and management of Silver–Russell syndrome: first international consensus statement". Nature Reviews Endocrinology. 13 (2): 105–124. doi:10.1038/nrendo.2016.138. hdl:1765/108227. ISSN 1759-5029. PMID 27585961. S2CID 13729923.

childgrowthfoundation.org

Silver-Russell Syndrome (2.0 ed.). United Kingdom: Child Growth Foundation. March 2021. p. 19. Retrieved 9 April 2022.

doi.org

Gilbert, Patricia (1996). "Silver—Russell syndrome". The A-Z Reference Book of Syndromes and Inherited Disorders (second ed.). pp. 271–273. doi:10.1007/978-1-4899-6918-7_71. ISBN 978-0-412-64120-6.
Wollmann, H. A.; Kirchner, T; Enders, H; Preece, M. A.; Ranke, M. B. (1995). "Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients". European Journal of Pediatrics. 154 (12): 958–68. doi:10.1007/bf01958638. PMID 8801103. S2CID 21595433.
De Crescenzo, Agostina; Citro, Valentina; Freschi, Andrea; Sparago, Angela; Palumbo, Orazio; Cubellis, Maria Vittoria; Carella, Massimo; Castelluccio, Pia; Cavaliere, Maria Luigia; Cerrato, Flavia; Riccio, Andrea (June 2015). "A splicing mutation of the HMGA2 gene is associated with Silver–Russell syndrome phenotype". Journal of Human Genetics. 60 (6): 287–293. doi:10.1038/jhg.2015.29. ISSN 1435-232X. PMID 25809938.
Bartholdi, D; Krajewska-Walasek, M; Ounap, K; Gaspar, H; Chrzanowska, K H; Ilyana, H; Kayserili, H; Lurie, I W; Schinzel, A; Baumer, A (2008). "Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): Results from a large cohort of patients with SRS and SRS-like phenotypes" (PDF). Journal of Medical Genetics. 46 (3): 192–7. doi:10.1136/jmg.2008.061820. PMID 19066168. S2CID 29211777. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-10-31.
Eggermann, Thomas; Begemann, Matthias; Binder, Gerhard; Spengler, Sabrina (2010). "Silver-Russell syndrome: genetic basis and molecular genetic testing". Orphanet Journal of Rare Diseases. 5 (1): 19. doi:10.1186/1750-1172-5-19. ISSN 1750-1172. PMC 2907323. PMID 20573229.
Hattori, Atsushi; Okuyama, Torayuki; So, Tetsumin; Kosuga, Motomichi; Ichimoto, Keiko; Murayama, Kei; Kagami, Masayo; Fukami, Maki; Fukuhara, Yasuyuki (2022-09-12). "Maternal uniparental disomy of chromosome 7 underlying argininosuccinic aciduria and Silver-Russell syndrome". Human Genome Variation. 9 (1): 32. doi:10.1038/s41439-022-00211-y. ISSN 2054-345X. PMC 9468177. PMID 36097158.
Ishida, Miho (April 2016). "New developments in Silver–Russell syndrome and implications for clinical practice". Epigenomics. 8 (4): 563–580. doi:10.2217/epi-2015-0010. ISSN 1750-1911. PMC 4928503. PMID 27066913.
Butler, M. G. (2009). "Genomic imprinting disorders in humans: A mini-review". Journal of Assisted Reproduction and Genetics. 26 (9–10): 477–86. doi:10.1007/s10815-009-9353-3. PMC 2788689. PMID 19844787.
Spengler, S.; Schonherr, N.; Binder, G.; Wollmann, H. A.; Fricke-Otto, S.; Muhlenberg, R.; Denecke, B.; Baudis, M.; Eggermann, T. (2009-09-16). "Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome" (PDF). Journal of Medical Genetics. 47 (5): 356–360. doi:10.1136/jmg.2009.070052. ISSN 0022-2593. PMID 19762329. S2CID 30653418. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-12-12.
Wakeling, Emma L.; Brioude, Frédéric; Lokulo-Sodipe, Oluwakemi; O'Connell, Susan M.; Salem, Jennifer; Bliek, Jet; Canton, Ana P. M.; Chrzanowska, Krystyna H.; Davies, Justin H. (2016-09-02). "Diagnosis and management of Silver–Russell syndrome: first international consensus statement". Nature Reviews Endocrinology. 13 (2): 105–124. doi:10.1038/nrendo.2016.138. hdl:1765/108227. ISSN 1759-5029. PMID 27585961. S2CID 13729923.
Rakover, Y.; Dietsch, S.; Ambler, G. R.; Chock, C.; Thomsett, M.; Cowell, C. T. (1996). "Growth hormone therapy in Silver Russell Syndrome: 5 years experience of the Australian and New Zealand Growth database (OZGROW)". European Journal of Pediatrics. 155 (10): 851–7. doi:10.1007/BF02282833. PMID 8891553. S2CID 11550940.
Silver, H. K.; Kiyasu, W; George, J; Deamer, W. C. (1953). "Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins". Pediatrics. 12 (4): 368–76. doi:10.1542/peds.12.4.368. PMID 13099907. S2CID 22644845.

handle.net

hdl.handle.net

Wakeling, Emma L.; Brioude, Frédéric; Lokulo-Sodipe, Oluwakemi; O'Connell, Susan M.; Salem, Jennifer; Bliek, Jet; Canton, Ana P. M.; Chrzanowska, Krystyna H.; Davies, Justin H. (2016-09-02). "Diagnosis and management of Silver–Russell syndrome: first international consensus statement". Nature Reviews Endocrinology. 13 (2): 105–124. doi:10.1038/nrendo.2016.138. hdl:1765/108227. ISSN 1759-5029. PMID 27585961. S2CID 13729923.

nature.com

De Crescenzo, Agostina; Citro, Valentina; Freschi, Andrea; Sparago, Angela; Palumbo, Orazio; Cubellis, Maria Vittoria; Carella, Massimo; Castelluccio, Pia; Cavaliere, Maria Luigia; Cerrato, Flavia; Riccio, Andrea (June 2015). "A splicing mutation of the HMGA2 gene is associated with Silver–Russell syndrome phenotype". Journal of Human Genetics. 60 (6): 287–293. doi:10.1038/jhg.2015.29. ISSN 1435-232X. PMID 25809938.

nih.gov

pubmed.ncbi.nlm.nih.gov

Wollmann, H. A.; Kirchner, T; Enders, H; Preece, M. A.; Ranke, M. B. (1995). "Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients". European Journal of Pediatrics. 154 (12): 958–68. doi:10.1007/bf01958638. PMID 8801103. S2CID 21595433.
De Crescenzo, Agostina; Citro, Valentina; Freschi, Andrea; Sparago, Angela; Palumbo, Orazio; Cubellis, Maria Vittoria; Carella, Massimo; Castelluccio, Pia; Cavaliere, Maria Luigia; Cerrato, Flavia; Riccio, Andrea (June 2015). "A splicing mutation of the HMGA2 gene is associated with Silver–Russell syndrome phenotype". Journal of Human Genetics. 60 (6): 287–293. doi:10.1038/jhg.2015.29. ISSN 1435-232X. PMID 25809938.
Bartholdi, D; Krajewska-Walasek, M; Ounap, K; Gaspar, H; Chrzanowska, K H; Ilyana, H; Kayserili, H; Lurie, I W; Schinzel, A; Baumer, A (2008). "Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): Results from a large cohort of patients with SRS and SRS-like phenotypes" (PDF). Journal of Medical Genetics. 46 (3): 192–7. doi:10.1136/jmg.2008.061820. PMID 19066168. S2CID 29211777. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-10-31.
Eggermann, Thomas; Begemann, Matthias; Binder, Gerhard; Spengler, Sabrina (2010). "Silver-Russell syndrome: genetic basis and molecular genetic testing". Orphanet Journal of Rare Diseases. 5 (1): 19. doi:10.1186/1750-1172-5-19. ISSN 1750-1172. PMC 2907323. PMID 20573229.
Hattori, Atsushi; Okuyama, Torayuki; So, Tetsumin; Kosuga, Motomichi; Ichimoto, Keiko; Murayama, Kei; Kagami, Masayo; Fukami, Maki; Fukuhara, Yasuyuki (2022-09-12). "Maternal uniparental disomy of chromosome 7 underlying argininosuccinic aciduria and Silver-Russell syndrome". Human Genome Variation. 9 (1): 32. doi:10.1038/s41439-022-00211-y. ISSN 2054-345X. PMC 9468177. PMID 36097158.
Ishida, Miho (April 2016). "New developments in Silver–Russell syndrome and implications for clinical practice". Epigenomics. 8 (4): 563–580. doi:10.2217/epi-2015-0010. ISSN 1750-1911. PMC 4928503. PMID 27066913.
Butler, M. G. (2009). "Genomic imprinting disorders in humans: A mini-review". Journal of Assisted Reproduction and Genetics. 26 (9–10): 477–86. doi:10.1007/s10815-009-9353-3. PMC 2788689. PMID 19844787.
Spengler, S.; Schonherr, N.; Binder, G.; Wollmann, H. A.; Fricke-Otto, S.; Muhlenberg, R.; Denecke, B.; Baudis, M.; Eggermann, T. (2009-09-16). "Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome" (PDF). Journal of Medical Genetics. 47 (5): 356–360. doi:10.1136/jmg.2009.070052. ISSN 0022-2593. PMID 19762329. S2CID 30653418. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-12-12.
Wakeling, Emma L.; Brioude, Frédéric; Lokulo-Sodipe, Oluwakemi; O'Connell, Susan M.; Salem, Jennifer; Bliek, Jet; Canton, Ana P. M.; Chrzanowska, Krystyna H.; Davies, Justin H. (2016-09-02). "Diagnosis and management of Silver–Russell syndrome: first international consensus statement". Nature Reviews Endocrinology. 13 (2): 105–124. doi:10.1038/nrendo.2016.138. hdl:1765/108227. ISSN 1759-5029. PMID 27585961. S2CID 13729923.
Rakover, Y.; Dietsch, S.; Ambler, G. R.; Chock, C.; Thomsett, M.; Cowell, C. T. (1996). "Growth hormone therapy in Silver Russell Syndrome: 5 years experience of the Australian and New Zealand Growth database (OZGROW)". European Journal of Pediatrics. 155 (10): 851–7. doi:10.1007/BF02282833. PMID 8891553. S2CID 11550940.
Russell, A (1954). "A syndrome of intra-uterine dwarfism recognizable at birth with cranio-facial dysostosis, disproportionately short arms, and other anomalies (5 examples)". Proceedings of the Royal Society of Medicine. 47 (12): 1040–4. PMC 1919148. PMID 13237189.
Silver, H. K.; Kiyasu, W; George, J; Deamer, W. C. (1953). "Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins". Pediatrics. 12 (4): 368–76. doi:10.1542/peds.12.4.368. PMID 13099907. S2CID 22644845.

ncbi.nlm.nih.gov

Eggermann, Thomas; Begemann, Matthias; Binder, Gerhard; Spengler, Sabrina (2010). "Silver-Russell syndrome: genetic basis and molecular genetic testing". Orphanet Journal of Rare Diseases. 5 (1): 19. doi:10.1186/1750-1172-5-19. ISSN 1750-1172. PMC 2907323. PMID 20573229.
Hattori, Atsushi; Okuyama, Torayuki; So, Tetsumin; Kosuga, Motomichi; Ichimoto, Keiko; Murayama, Kei; Kagami, Masayo; Fukami, Maki; Fukuhara, Yasuyuki (2022-09-12). "Maternal uniparental disomy of chromosome 7 underlying argininosuccinic aciduria and Silver-Russell syndrome". Human Genome Variation. 9 (1): 32. doi:10.1038/s41439-022-00211-y. ISSN 2054-345X. PMC 9468177. PMID 36097158.
Ishida, Miho (April 2016). "New developments in Silver–Russell syndrome and implications for clinical practice". Epigenomics. 8 (4): 563–580. doi:10.2217/epi-2015-0010. ISSN 1750-1911. PMC 4928503. PMID 27066913.
Butler, M. G. (2009). "Genomic imprinting disorders in humans: A mini-review". Journal of Assisted Reproduction and Genetics. 26 (9–10): 477–86. doi:10.1007/s10815-009-9353-3. PMC 2788689. PMID 19844787.
Russell, A (1954). "A syndrome of intra-uterine dwarfism recognizable at birth with cranio-facial dysostosis, disproportionately short arms, and other anomalies (5 examples)". Proceedings of the Royal Society of Medicine. 47 (12): 1040–4. PMC 1919148. PMID 13237189.

omim.org

"Silver-Russell Syndrome; SRS". OMIM.

patient.info

"Russell-Silver Syndrome". patient.info. February 2017.

semanticscholar.org

api.semanticscholar.org

Wollmann, H. A.; Kirchner, T; Enders, H; Preece, M. A.; Ranke, M. B. (1995). "Growth and symptoms in Silver-Russell syndrome: Review on the basis of 386 patients". European Journal of Pediatrics. 154 (12): 958–68. doi:10.1007/bf01958638. PMID 8801103. S2CID 21595433.
Bartholdi, D; Krajewska-Walasek, M; Ounap, K; Gaspar, H; Chrzanowska, K H; Ilyana, H; Kayserili, H; Lurie, I W; Schinzel, A; Baumer, A (2008). "Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): Results from a large cohort of patients with SRS and SRS-like phenotypes" (PDF). Journal of Medical Genetics. 46 (3): 192–7. doi:10.1136/jmg.2008.061820. PMID 19066168. S2CID 29211777. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-10-31.
Spengler, S.; Schonherr, N.; Binder, G.; Wollmann, H. A.; Fricke-Otto, S.; Muhlenberg, R.; Denecke, B.; Baudis, M.; Eggermann, T. (2009-09-16). "Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome" (PDF). Journal of Medical Genetics. 47 (5): 356–360. doi:10.1136/jmg.2009.070052. ISSN 0022-2593. PMID 19762329. S2CID 30653418. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-12-12.
Wakeling, Emma L.; Brioude, Frédéric; Lokulo-Sodipe, Oluwakemi; O'Connell, Susan M.; Salem, Jennifer; Bliek, Jet; Canton, Ana P. M.; Chrzanowska, Krystyna H.; Davies, Justin H. (2016-09-02). "Diagnosis and management of Silver–Russell syndrome: first international consensus statement". Nature Reviews Endocrinology. 13 (2): 105–124. doi:10.1038/nrendo.2016.138. hdl:1765/108227. ISSN 1759-5029. PMID 27585961. S2CID 13729923.
Rakover, Y.; Dietsch, S.; Ambler, G. R.; Chock, C.; Thomsett, M.; Cowell, C. T. (1996). "Growth hormone therapy in Silver Russell Syndrome: 5 years experience of the Australian and New Zealand Growth database (OZGROW)". European Journal of Pediatrics. 155 (10): 851–7. doi:10.1007/BF02282833. PMID 8891553. S2CID 11550940.
Silver, H. K.; Kiyasu, W; George, J; Deamer, W. C. (1953). "Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins". Pediatrics. 12 (4): 368–76. doi:10.1542/peds.12.4.368. PMID 13099907. S2CID 22644845.

uzh.ch

zora.uzh.ch

Bartholdi, D; Krajewska-Walasek, M; Ounap, K; Gaspar, H; Chrzanowska, K H; Ilyana, H; Kayserili, H; Lurie, I W; Schinzel, A; Baumer, A (2008). "Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): Results from a large cohort of patients with SRS and SRS-like phenotypes" (PDF). Journal of Medical Genetics. 46 (3): 192–7. doi:10.1136/jmg.2008.061820. PMID 19066168. S2CID 29211777. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-10-31.
Spengler, S.; Schonherr, N.; Binder, G.; Wollmann, H. A.; Fricke-Otto, S.; Muhlenberg, R.; Denecke, B.; Baudis, M.; Eggermann, T. (2009-09-16). "Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome" (PDF). Journal of Medical Genetics. 47 (5): 356–360. doi:10.1136/jmg.2009.070052. ISSN 0022-2593. PMID 19762329. S2CID 30653418. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-12-12.

web.archive.org

Bartholdi, D; Krajewska-Walasek, M; Ounap, K; Gaspar, H; Chrzanowska, K H; Ilyana, H; Kayserili, H; Lurie, I W; Schinzel, A; Baumer, A (2008). "Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): Results from a large cohort of patients with SRS and SRS-like phenotypes" (PDF). Journal of Medical Genetics. 46 (3): 192–7. doi:10.1136/jmg.2008.061820. PMID 19066168. S2CID 29211777. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-10-31.
Spengler, S.; Schonherr, N.; Binder, G.; Wollmann, H. A.; Fricke-Otto, S.; Muhlenberg, R.; Denecke, B.; Baudis, M.; Eggermann, T. (2009-09-16). "Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome" (PDF). Journal of Medical Genetics. 47 (5): 356–360. doi:10.1136/jmg.2009.070052. ISSN 0022-2593. PMID 19762329. S2CID 30653418. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-12-12.

whonamedit.com

synd/2892 at Who Named It?

worldcat.org

search.worldcat.org

De Crescenzo, Agostina; Citro, Valentina; Freschi, Andrea; Sparago, Angela; Palumbo, Orazio; Cubellis, Maria Vittoria; Carella, Massimo; Castelluccio, Pia; Cavaliere, Maria Luigia; Cerrato, Flavia; Riccio, Andrea (June 2015). "A splicing mutation of the HMGA2 gene is associated with Silver–Russell syndrome phenotype". Journal of Human Genetics. 60 (6): 287–293. doi:10.1038/jhg.2015.29. ISSN 1435-232X. PMID 25809938.
Eggermann, Thomas; Begemann, Matthias; Binder, Gerhard; Spengler, Sabrina (2010). "Silver-Russell syndrome: genetic basis and molecular genetic testing". Orphanet Journal of Rare Diseases. 5 (1): 19. doi:10.1186/1750-1172-5-19. ISSN 1750-1172. PMC 2907323. PMID 20573229.
Hattori, Atsushi; Okuyama, Torayuki; So, Tetsumin; Kosuga, Motomichi; Ichimoto, Keiko; Murayama, Kei; Kagami, Masayo; Fukami, Maki; Fukuhara, Yasuyuki (2022-09-12). "Maternal uniparental disomy of chromosome 7 underlying argininosuccinic aciduria and Silver-Russell syndrome". Human Genome Variation. 9 (1): 32. doi:10.1038/s41439-022-00211-y. ISSN 2054-345X. PMC 9468177. PMID 36097158.
Ishida, Miho (April 2016). "New developments in Silver–Russell syndrome and implications for clinical practice". Epigenomics. 8 (4): 563–580. doi:10.2217/epi-2015-0010. ISSN 1750-1911. PMC 4928503. PMID 27066913.
Spengler, S.; Schonherr, N.; Binder, G.; Wollmann, H. A.; Fricke-Otto, S.; Muhlenberg, R.; Denecke, B.; Baudis, M.; Eggermann, T. (2009-09-16). "Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome" (PDF). Journal of Medical Genetics. 47 (5): 356–360. doi:10.1136/jmg.2009.070052. ISSN 0022-2593. PMID 19762329. S2CID 30653418. Archived from the original (PDF) on 2021-05-03. Retrieved 2019-12-12.
Wakeling, Emma L.; Brioude, Frédéric; Lokulo-Sodipe, Oluwakemi; O'Connell, Susan M.; Salem, Jennifer; Bliek, Jet; Canton, Ana P. M.; Chrzanowska, Krystyna H.; Davies, Justin H. (2016-09-02). "Diagnosis and management of Silver–Russell syndrome: first international consensus statement". Nature Reviews Endocrinology. 13 (2): 105–124. doi:10.1038/nrendo.2016.138. hdl:1765/108227. ISSN 1759-5029. PMID 27585961. S2CID 13729923.