Shivendra Kishore

Rostock, MV 18055, Germany

Last Updated: 09/26/2026

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Found 12 publications

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders.

De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders.

Journal: American journal of human genetics

Published: January 08, 2019

Clinical Exome Sequencing unravels new disease-causing mutations in the myeloproliferative neoplasms: A pilot study in patients from the state of Qatar.

Clinical Exome Sequencing unravels new disease-causing mutations in the myeloproliferative neoplasms: A pilot study in patients from the state of Qatar.

Journal: Gene

Published: October 13, 2018

Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders.

Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders.

Journal: Journal of neurodevelopmental disorders

Published: September 18, 2018

MINA-1 and WAGO-4 are part of regulatory network coordinating germ cell death and RNAi in C. elegans.

MINA-1 and WAGO-4 are part of regulatory network coordinating germ cell death and RNAi in C. elegans.

Journal: Cell death and differentiation

Published: June 29, 2018

Development of an evidence-based algorithm that optimizes sensitivity and specificity in ES-based diagnostics of a clinically heterogeneous patient population.

Development of an evidence-based algorithm that optimizes sensitivity and specificity in ES-based diagnostics of a clinically heterogeneous patient population.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 12, 2017

17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report.

17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report.

Journal: BMC medical genetics

Published: June 07, 2017

Clinical exome sequencing: results from 2819 samples reflecting 1000 families.

Clinical exome sequencing: results from 2819 samples reflecting 1000 families.

Journal: European journal of human genetics : EJHG

Published: April 01, 2016

HIV-1 RNAs are Not Part of the Argonaute 2 Associated RNA Interference Pathway in Macrophages.

HIV-1 RNAs are Not Part of the Argonaute 2 Associated RNA Interference Pathway in Macrophages.

Journal: PloS one

Published: January 22, 2015

miR-CLIP capture of a miRNA targetome uncovers a lincRNA H19-miR-106a interaction.

miR-CLIP capture of a miRNA targetome uncovers a lincRNA H19-miR-106a interaction.

Journal: Nature chemical biology

Published: September 07, 2014

3'-UTR poly(T/U) tract deletions and altered expression of EWSR1 are a hallmark of mismatch repair-deficient cancers.

3'-UTR poly(T/U) tract deletions and altered expression of EWSR1 are a hallmark of mismatch repair-deficient cancers.

Journal: Cancer research

Published: October 26, 2013

Modeling the binding specificity of the RNA-binding protein GLD-1 suggests a function of coding region-located sites in translational repression.

Modeling the binding specificity of the RNA-binding protein GLD-1 suggests a function of coding region-located sites in translational repression.

Journal: RNA (New York, N.Y.)

Published: August 27, 2013

Insights into snoRNA biogenesis and processing from PAR-CLIP of snoRNA core proteins and small RNA sequencing.

Insights into snoRNA biogenesis and processing from PAR-CLIP of snoRNA core proteins and small RNA sequencing.

Journal: Genome biology

Published: March 18, 2013

Showing 1-12 of 12

Last Updated: 09/26/2026