Emberger syndrome (English Wikipedia)

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

refsWebsite

Global rank English rank

20nih.gov

4^th place

12doi.org

2^nd place

4semanticscholar.org

11^th place

8^th place

2sgul.ac.uk

low place

doi.org

Crispino JD, Horwitz MS (April 2017). "GATA factor mutations in hematologic disease". Blood. 129 (15): 2103–2110. doi:10.1182/blood-2016-09-687889. PMC 5391620. PMID 28179280.
Rastogi N, Abraham RS, Chadha R, Thakkar D, Kohli S, Nivargi S, Prakash Yadav S (November 2017). "Successful Nonmyeloablative Allogeneic Stem Cell Transplant in a Child With Emberger Syndrome and GATA2 Mutation". Journal of Pediatric Hematology/Oncology. 40 (6): e383 – e388. doi:10.1097/MPH.0000000000000995. PMID 29189513. S2CID 19080505.
Hirabayashi S, Wlodarski MW, Kozyra E, Niemeyer CM (August 2017). "Heterogeneity of GATA2-related myeloid neoplasms". International Journal of Hematology. 106 (2): 175–182. doi:10.1007/s12185-017-2285-2. PMID 28643018.
Wlodarski MW, Collin M, Horwitz MS (April 2017). "GATA2 deficiency and related myeloid neoplasms". Seminars in Hematology. 54 (2): 81–86. doi:10.1053/j.seminhematol.2017.05.002. PMC 5650112. PMID 28637621.
Ostergaard P, Simpson MA, Connell FC, Steward CG, Brice G, Woollard WJ, Dafou D, Kilo T, Smithson S, Lunt P, Murday VA, Hodgson S, Keenan R, Pilz DT, Martinez-Corral I, Makinen T, Mortimer PS, Jeffery S, Trembath RC, Mansour S (September 2011). "Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)" (PDF). Nature Genetics. 43 (10): 929–31. doi:10.1038/ng.923. PMID 21892158. S2CID 23449974.
Katsumura KR, Bresnick EH (April 2017). "The GATA factor revolution in hematology". Blood. 129 (15): 2092–2102. doi:10.1182/blood-2016-09-687871. PMC 5391619. PMID 28179282.
Mansour S, Connell F, Steward C, Ostergaard P, Brice G, Smithson S, Lunt P, Jeffery S, Dokal I, Vulliamy T, Gibson B, Hodgson S, Cottrell S, Kiely L, Tinworth L, Kalidas K, Mufti G, Cornish J, Keenan R, Mortimer P, Murday V (September 2010). "Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new cases". American Journal of Medical Genetics. Part A. 152A (9): 2287–96. doi:10.1002/ajmg.a.33445. PMID 20803646. S2CID 205312771.
Brambila-Tapia AJ, García-Ortiz JE, Brouillard P, Nguyen HL, Vikkula M, Ríos-González BE, Sandoval-Muñiz RJ, Sandoval-Talamantes AK, Bobadilla-Morales L, Corona-Rivera JR, Arnaud-Lopez L (September 2017). "GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome". Hematology (Amsterdam, Netherlands). 22 (8): 467–471. doi:10.1080/10245332.2017.1294551. PMID 28271814.
Babushok DV, Bessler M (March 2015). "Genetic predisposition syndromes: when should they be considered in the work-up of MDS?". Best Practice & Research. Clinical Haematology. 28 (1): 55–68. doi:10.1016/j.beha.2014.11.004. PMC 4323616. PMID 25659730.
Chlon TM, Crispino JD (November 2012). "Combinatorial regulation of tissue specification by GATA and FOG factors". Development. 139 (21): 3905–16. doi:10.1242/dev.080440. PMC 3472596. PMID 23048181.
Hsu AP, McReynolds LJ, Holland SM (February 2015). "GATA2 deficiency". Current Opinion in Allergy and Clinical Immunology. 15 (1): 104–9. doi:10.1097/ACI.0000000000000126. PMC 4342850. PMID 25397911.
Ostergaard, P; Simpson, MA; Connell, FC; Steward, CG; Brice, G; Woollard, WJ; Dafou, D; Kilo, T; Smithson, S; Lunt, P; Murday, VA; Hodgson, S; Keenan, R; Pilz, DT; Martinez-Corral, I; Makinen, T; Mortimer, PS; Jeffery, S; Trembath, RC; Mansour, S (4 September 2011). "Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)" (PDF). Nature Genetics. 43 (10): 929–31. doi:10.1038/ng.923. PMID 21892158. S2CID 23449974.

nih.gov

pubmed.ncbi.nlm.nih.gov

Crispino JD, Horwitz MS (April 2017). "GATA factor mutations in hematologic disease". Blood. 129 (15): 2103–2110. doi:10.1182/blood-2016-09-687889. PMC 5391620. PMID 28179280.
Rastogi N, Abraham RS, Chadha R, Thakkar D, Kohli S, Nivargi S, Prakash Yadav S (November 2017). "Successful Nonmyeloablative Allogeneic Stem Cell Transplant in a Child With Emberger Syndrome and GATA2 Mutation". Journal of Pediatric Hematology/Oncology. 40 (6): e383 – e388. doi:10.1097/MPH.0000000000000995. PMID 29189513. S2CID 19080505.
Hirabayashi S, Wlodarski MW, Kozyra E, Niemeyer CM (August 2017). "Heterogeneity of GATA2-related myeloid neoplasms". International Journal of Hematology. 106 (2): 175–182. doi:10.1007/s12185-017-2285-2. PMID 28643018.
Wlodarski MW, Collin M, Horwitz MS (April 2017). "GATA2 deficiency and related myeloid neoplasms". Seminars in Hematology. 54 (2): 81–86. doi:10.1053/j.seminhematol.2017.05.002. PMC 5650112. PMID 28637621.
Ostergaard P, Simpson MA, Connell FC, Steward CG, Brice G, Woollard WJ, Dafou D, Kilo T, Smithson S, Lunt P, Murday VA, Hodgson S, Keenan R, Pilz DT, Martinez-Corral I, Makinen T, Mortimer PS, Jeffery S, Trembath RC, Mansour S (September 2011). "Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)" (PDF). Nature Genetics. 43 (10): 929–31. doi:10.1038/ng.923. PMID 21892158. S2CID 23449974.
Katsumura KR, Bresnick EH (April 2017). "The GATA factor revolution in hematology". Blood. 129 (15): 2092–2102. doi:10.1182/blood-2016-09-687871. PMC 5391619. PMID 28179282.
Mansour S, Connell F, Steward C, Ostergaard P, Brice G, Smithson S, Lunt P, Jeffery S, Dokal I, Vulliamy T, Gibson B, Hodgson S, Cottrell S, Kiely L, Tinworth L, Kalidas K, Mufti G, Cornish J, Keenan R, Mortimer P, Murday V (September 2010). "Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new cases". American Journal of Medical Genetics. Part A. 152A (9): 2287–96. doi:10.1002/ajmg.a.33445. PMID 20803646. S2CID 205312771.
Brambila-Tapia AJ, García-Ortiz JE, Brouillard P, Nguyen HL, Vikkula M, Ríos-González BE, Sandoval-Muñiz RJ, Sandoval-Talamantes AK, Bobadilla-Morales L, Corona-Rivera JR, Arnaud-Lopez L (September 2017). "GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome". Hematology (Amsterdam, Netherlands). 22 (8): 467–471. doi:10.1080/10245332.2017.1294551. PMID 28271814.
Babushok DV, Bessler M (March 2015). "Genetic predisposition syndromes: when should they be considered in the work-up of MDS?". Best Practice & Research. Clinical Haematology. 28 (1): 55–68. doi:10.1016/j.beha.2014.11.004. PMC 4323616. PMID 25659730.
Chlon TM, Crispino JD (November 2012). "Combinatorial regulation of tissue specification by GATA and FOG factors". Development. 139 (21): 3905–16. doi:10.1242/dev.080440. PMC 3472596. PMID 23048181.
Hsu AP, McReynolds LJ, Holland SM (February 2015). "GATA2 deficiency". Current Opinion in Allergy and Clinical Immunology. 15 (1): 104–9. doi:10.1097/ACI.0000000000000126. PMC 4342850. PMID 25397911.
Emberger JM, Navarro M, Dejean M, Izarn P (October 1979). "[Deaf-mutism, lymphedema of the lower limbs and hematological abnormalities (acute leukemia, cytopenia) with autosomal dominant transmission]". Journal de Génétique Humaine (in French). 27 (3): 237–45. PMID 295075.
Ostergaard, P; Simpson, MA; Connell, FC; Steward, CG; Brice, G; Woollard, WJ; Dafou, D; Kilo, T; Smithson, S; Lunt, P; Murday, VA; Hodgson, S; Keenan, R; Pilz, DT; Martinez-Corral, I; Makinen, T; Mortimer, PS; Jeffery, S; Trembath, RC; Mansour, S (4 September 2011). "Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)" (PDF). Nature Genetics. 43 (10): 929–31. doi:10.1038/ng.923. PMID 21892158. S2CID 23449974.

ncbi.nlm.nih.gov

Crispino JD, Horwitz MS (April 2017). "GATA factor mutations in hematologic disease". Blood. 129 (15): 2103–2110. doi:10.1182/blood-2016-09-687889. PMC 5391620. PMID 28179280.
Wlodarski MW, Collin M, Horwitz MS (April 2017). "GATA2 deficiency and related myeloid neoplasms". Seminars in Hematology. 54 (2): 81–86. doi:10.1053/j.seminhematol.2017.05.002. PMC 5650112. PMID 28637621.
Katsumura KR, Bresnick EH (April 2017). "The GATA factor revolution in hematology". Blood. 129 (15): 2092–2102. doi:10.1182/blood-2016-09-687871. PMC 5391619. PMID 28179282.
Babushok DV, Bessler M (March 2015). "Genetic predisposition syndromes: when should they be considered in the work-up of MDS?". Best Practice & Research. Clinical Haematology. 28 (1): 55–68. doi:10.1016/j.beha.2014.11.004. PMC 4323616. PMID 25659730.
Chlon TM, Crispino JD (November 2012). "Combinatorial regulation of tissue specification by GATA and FOG factors". Development. 139 (21): 3905–16. doi:10.1242/dev.080440. PMC 3472596. PMID 23048181.
"GATA2 GATA binding protein 2 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov.
Hsu AP, McReynolds LJ, Holland SM (February 2015). "GATA2 deficiency". Current Opinion in Allergy and Clinical Immunology. 15 (1): 104–9. doi:10.1097/ACI.0000000000000126. PMC 4342850. PMID 25397911.

semanticscholar.org

api.semanticscholar.org

Rastogi N, Abraham RS, Chadha R, Thakkar D, Kohli S, Nivargi S, Prakash Yadav S (November 2017). "Successful Nonmyeloablative Allogeneic Stem Cell Transplant in a Child With Emberger Syndrome and GATA2 Mutation". Journal of Pediatric Hematology/Oncology. 40 (6): e383 – e388. doi:10.1097/MPH.0000000000000995. PMID 29189513. S2CID 19080505.
Ostergaard P, Simpson MA, Connell FC, Steward CG, Brice G, Woollard WJ, Dafou D, Kilo T, Smithson S, Lunt P, Murday VA, Hodgson S, Keenan R, Pilz DT, Martinez-Corral I, Makinen T, Mortimer PS, Jeffery S, Trembath RC, Mansour S (September 2011). "Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)" (PDF). Nature Genetics. 43 (10): 929–31. doi:10.1038/ng.923. PMID 21892158. S2CID 23449974.
Mansour S, Connell F, Steward C, Ostergaard P, Brice G, Smithson S, Lunt P, Jeffery S, Dokal I, Vulliamy T, Gibson B, Hodgson S, Cottrell S, Kiely L, Tinworth L, Kalidas K, Mufti G, Cornish J, Keenan R, Mortimer P, Murday V (September 2010). "Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new cases". American Journal of Medical Genetics. Part A. 152A (9): 2287–96. doi:10.1002/ajmg.a.33445. PMID 20803646. S2CID 205312771.
Ostergaard, P; Simpson, MA; Connell, FC; Steward, CG; Brice, G; Woollard, WJ; Dafou, D; Kilo, T; Smithson, S; Lunt, P; Murday, VA; Hodgson, S; Keenan, R; Pilz, DT; Martinez-Corral, I; Makinen, T; Mortimer, PS; Jeffery, S; Trembath, RC; Mansour, S (4 September 2011). "Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)" (PDF). Nature Genetics. 43 (10): 929–31. doi:10.1038/ng.923. PMID 21892158. S2CID 23449974.

sgul.ac.uk

openaccess.sgul.ac.uk

Ostergaard P, Simpson MA, Connell FC, Steward CG, Brice G, Woollard WJ, Dafou D, Kilo T, Smithson S, Lunt P, Murday VA, Hodgson S, Keenan R, Pilz DT, Martinez-Corral I, Makinen T, Mortimer PS, Jeffery S, Trembath RC, Mansour S (September 2011). "Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)" (PDF). Nature Genetics. 43 (10): 929–31. doi:10.1038/ng.923. PMID 21892158. S2CID 23449974.
Ostergaard, P; Simpson, MA; Connell, FC; Steward, CG; Brice, G; Woollard, WJ; Dafou, D; Kilo, T; Smithson, S; Lunt, P; Murday, VA; Hodgson, S; Keenan, R; Pilz, DT; Martinez-Corral, I; Makinen, T; Mortimer, PS; Jeffery, S; Trembath, RC; Mansour, S (4 September 2011). "Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)" (PDF). Nature Genetics. 43 (10): 929–31. doi:10.1038/ng.923. PMID 21892158. S2CID 23449974.