(Q34984094)

5 August 2017

Acquired mutations in TET2 are common in myelodysplastic syndromes (English)

1 reference

Adrianus Henricus Maria Geurts van Kessel

5 August 2017

9

object named as

Ad Geurts van Kessel

0 references

Peter Vandenberghe

object named as

Peter Vandenberghe

15

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Gregor Verhoef

12

object named as

Gregor E Verhoef

1 reference

5 August 2017

Saskia M C Langemeijer

1

1 reference

5 August 2017

Roland P Kuiper

2

1 reference

5 August 2017

Marieke Berends

3

1 reference

5 August 2017

Ruth Knops

4

1 reference

5 August 2017

Mariam G Aslanyan

5

1 reference

5 August 2017

Marion Massop

6

1 reference

5 August 2017

Ellen Stevens-Linders

7

1 reference

5 August 2017

Patricia van Hoogen

8

1 reference

5 August 2017

Ad Geurts van Kessel

9

1 reference

5 August 2017

Reinier A P Raymakers

10

1 reference

5 August 2017

Eveline J Kamping

11

1 reference

5 August 2017

Estelle Verburgh

13

1 reference

5 August 2017

Anne Hagemeijer

14

1 reference

5 August 2017

Theo de Witte

16

1 reference

5 August 2017

Bert A van der Reijden

17

1 reference

5 August 2017

Joop H Jansen

18

1 reference

5 August 2017

language of work or name

English

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publication date

31 May 2009

1 reference

5 August 2017

1 reference

5 August 2017

41

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5 August 2017

838-842

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5 August 2017

7

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.391

5 August 2017

0 references

cites work

Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes

1 reference

12 December 2020

Haploinsufficiency of RPS14 in 5q- syndrome is associated with deregulation of ribosomal- and translation-related genes

1 reference

12 December 2020

New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients

1 reference

12 December 2020

Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML

1 reference

12 December 2020

Myelodysplastic syndromes: molecular pathogenesis and genomic changes

1 reference

12 December 2020

Myelodysplastic syndromes.

1 reference

12 December 2020

Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays

1 reference

12 December 2020

Nomenclature for the description of human sequence variations.

1 reference

12 December 2020

Myelodysplastic syndromes

1 reference

12 December 2020

Global variation in copy number in the human genome

1 reference

12 December 2020

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

1 reference

12 December 2020

SNP array karyotyping allows for the detection of uniparental disomy and cryptic chromosomal abnormalities in MDS/MPD-U and MPD.

1 reference

12 December 2020

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen

1 reference

12 December 2020

Common 4q24 deletion in four cases of hematopoietic malignancy: early stem cell involvement?

1 reference

12 December 2020

250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies

1 reference

12 December 2020

Different genetic pathways in leukemogenesis for patients presenting with therapy-related myelodysplasia and therapy-related acute myeloid leukemia

1 reference

12 December 2020

The mitochondrial 13513G>A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff–Parkinson–White

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.391

1 reference

5 August 2017

1 reference