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Collection : Newcastle University Library Eprints Service

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Integration of genetics and MRD to define low risk patients with B-cell precursor acute lymphoblastic leukaemia with intermediate MRD levels at the end of induction

Authors : Moorman AV; Enshaei A; Murdy D

Source: Leukemia, 2024

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Academic Journal

Medullary Sponge Kidney and Its Relationship with Primary Distal Renal Tubular Acidosis: Case Reports and a Comprehensive Genetics-First Approach

Authors : Van Den Berg G; Claus LR; Van Der Zwaag B

Source: Nephron, 2024

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Academic Journal

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

Authors : Towns C; Richer M; Jasaityte S

Source: npj Parkinson's Disease, December 2023

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Academic Journal

Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†

Authors : Machipisa T; Chishala C; Shaboodien G

Source: Circulation: Genomic and Precision Medicine, 1 February 2023

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Neuromuscular disease genetics in under-represented populations: increasing data diversity

Authors : Wilson LA; Macken WL; Perry LD

Source: Brain, 1 December 2023

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Genetics of validated Parkinson's disease subtypes in the Oxford Discovery and Tracking Parkinson's cohorts

Authors : Lawton M; Tan MMX; Ben-Shlomo Y

Source: Journal of Neurology, Neurosurgery and Psychiatry, 1 September 2022

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Confirmation of the superior performance of the causal Graphical Analysis Using Genetics (cGAUGE) pipeline in comparison to various competing alternatives

Authors : Cordell HJ; Howey R

Source: Wellcome Open Research, 2022

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Academic Journal

Correction: Comparison of methods for transcriptome imputation through application to two common complex diseases (European Journal of Human Genetics, (2018), 26, 11, (1658-1667), 10.1038/s41431-018-0176-5)

Authors : Fryett JJ; Inshaw J; Morris AP

Source: European Journal of Human Genetics, 2020

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Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome

Authors : Ramsbottom SA; Thelwall PE; Wood KM

Source: Proceedings of the National Academy of Sciences of the United States of America, 14 January 2020

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Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

Authors : Beaumont RN; Warrington NM; Cavadino A

Source: Human Molecular Genetics, 15 February 2018

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فلترة النتائج

Integration of genetics and MRD to define low risk patients with B-cell precursor acute lymphoblastic leukaemia with intermediate MRD levels at the end of induction

Medullary Sponge Kidney and Its Relationship with Primary Distal Renal Tubular Acidosis: Case Reports and a Comprehensive Genetics-First Approach

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†

Neuromuscular disease genetics in under-represented populations: increasing data diversity

Genetics of validated Parkinson's disease subtypes in the Oxford Discovery and Tracking Parkinson's cohorts

Confirmation of the superior performance of the causal Graphical Analysis Using Genetics (cGAUGE) pipeline in comparison to various competing alternatives

Correction: Comparison of methods for transcriptome imputation through application to two common complex diseases (European Journal of Human Genetics, (2018), 26, 11, (1658-1667), 10.1038/s41431-018-0176-5)

Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome

Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

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