(Q35237812)

7 August 2017

title

Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome (English)

1 reference

7 August 2017

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1 reference

1

Tomasz Zemojtel

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Peter Robinson

25

Peter N Robinson

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Melissa Haendel

21

Melissa Haendel

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Stefan Mundlos

24

Stefan Mundlos

1 reference

7 August 2017

22

Damian Smedley

1 reference

7 August 2017

Amin Ardeshirdavani

18

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Sebastian Köhler

Sebastian Köhler

2

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Malte Spielmann

Malte Spielmann

10

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Peter Krawitz

Peter Krawitz

6

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Suzanna Lewis

20

Suzanna E Lewis

1 reference

7 August 2017

Luitgard Graul-Neumann

7

Luitgard Graul-Neumann

1 reference

7 August 2017

19

Yves Moreau

1 reference

7 August 2017

Björn Fischer-Zirnsak

1 reference

ORCID Public Data File 2021

Denise Horn

23

Denise Horn

1 reference

7 August 2017

Luisa Mackenroth

3

1 reference

7 August 2017

Marten Jäger

4

1 reference

7 August 2017

Jochen Hecht

5

1 reference

7 August 2017

Sandra Doelken

8

1 reference

7 August 2017

Nadja Ehmke

9

1 reference

7 August 2017

Nancy Christine Oien

11

1 reference

7 August 2017

Michal R Schweiger

12

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7 August 2017

Ulrike Krüger

13

1 reference

7 August 2017

Götz Frommer

14

1 reference

7 August 2017

Björn Fischer

15

1 reference

7 August 2017

Uwe Kornak

16

1 reference

7 August 2017

Ricarda Flöttmann

17

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7 August 2017

language of work or name

English

0 references

publication date

1 September 2014

1 reference

Science Translational Medicine

7 August 2017

published in

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7 August 2017

volume

6

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7 August 2017

issue

252

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7 August 2017

page(s)

252ra123

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Phenotype ontologies and cross-species analysis for translational research

7 August 2017

cites work

1 reference

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13 July 2018

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Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes

13 July 2018

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13 July 2018

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13 July 2018

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13 July 2018

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The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

13 July 2018

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13 July 2018

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Improved exome prioritization of disease genes through cross-species phenotype comparison

13 July 2018

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13 July 2018

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13 July 2018

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13 July 2018

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13 July 2018

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Diagnostic odyssey of patients with myotonic dystrophy

13 July 2018

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Quantifying single nucleotide variant detection sensitivity in exome sequencing

13 July 2018

1 reference

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Disease-targeted sequencing: a cornerstone in the clinic

13 July 2018

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Predicting mendelian disease-causing non-synonymous single nucleotide variants in exome sequencing studies

13 July 2018

1 reference

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Genes contributing to pain sensitivity in the normal population: an exome sequencing study.

13 July 2018

1 reference

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Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units

13 July 2018

1 reference

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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Bayesian ontology querying for accurate and noise-tolerant semantic searches

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

A public resource facilitating clinical use of genomes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

De novo mutations in MLL cause Wiedemann-Steiner syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Co-clustering phenome-genome for phenotype classification and disease gene discovery

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Deep phenotyping for precision medicine

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Representation of rare diseases in health information systems: the Orphanet approach to serve a wide range of end users

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

A systematic survey of loss-of-function variants in human protein-coding genes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Accurate and comprehensive sequencing of personal genomes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

PhenomeNET: a whole-phenome approach to disease gene discovery

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Deep sequencing of patient genomes for disease diagnosis: when will it become routine?

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®).

13 July 2018

1 reference

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Carrier testing for severe childhood recessive diseases by next-generation sequencing

13 July 2018

1 reference

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XLMR candidate mouse gene, Zcchc12 (Sizn1) is a novel marker of Cajal-Retzius cells

13 July 2018

1 reference

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The characterization of twenty sequenced human genomes

13 July 2018

1 reference

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MutationTaster evaluates disease-causing potential of sequence alterations

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

A method and server for predicting damaging missense mutations

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar Syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

The biological coherence of human phenome databases

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Exome sequencing identifies the cause of a mendelian disorder

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Clinical diagnostics in human genetics with semantic similarity searches in ontologies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

The DDB1-CUL4ADDB2 ubiquitin ligase is deficient in xeroderma pigmentosum group E and targets histone H2A at UV-damaged DNA sites

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Identification of the gene for Nance-Horan syndrome (NHS)

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

SIFT: Predicting amino acid changes that affect protein function

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

dbSNP: the NCBI database of genetic variation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Improved splice site detection in Genie

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Genetic disorders in children and young adults: a population study

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

The fibroblast growth factor receptor 2 p.Ala172Phe mutation in Pfeiffer syndrome--history repeating itself.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Diagnostic exome sequencing in persons with severe intellectual disability

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth disease.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Characterization of missense mutations and large deletions in the ALPL gene by sequencing and quantitative multiplex PCR of short fragments.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Molecular pathophysiology of mucolipidosis type IV: pH dysregulation of the mucolipin-1 cation channel.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4512639

Long-term survival in TARP syndrome and confirmation of RBM10 as the disease-causing gene

26 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1126%2FSCITRANSLMED.3009262

A novel mutation in the SHH long-range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25186178

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

[Childhood hypophosphatasia: a case report due to a novel mutation]

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25186178

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Delayed transport of tissue-nonspecific alkaline phosphatase with missense mutations causing hypophosphatasia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25186178

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1126/SCITRANSLMED.3009262

1 reference

7 August 2017

1 reference

7 August 2017

1 reference