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Showing 51–94 of 94 results

Advanced filters: Author: Amanda Lam Clear advanced filters

Acute myeloid leukaemia cells express high levels of androgen receptor but do not depend on androgen signaling for survival

Farideh Miraki-Moud
Linda Ariza-McNaughton
David C. Taussig
ResearchOpen Access11 Sept 2025
Leukemia

Volume: 39, P: 2895-2906
Prevalence and architecture of de novo mutations in developmental disorders

Whole-exome analysis of individuals with developmental disorders shows that de novo mutations can equally cause loss or altered protein function, but that most mutations causing altered protein function have not yet been described.

Jeremy F. McRae
Stephen Clayton
Matthew E. Hurles
Research25 Jan 2017
Nature

Volume: 542, P: 433-438
High-quality reference genome and annotation aids understanding of berry development for evergreen blueberry (Vaccinium darrowii)

Jiali Yu
Amanda M. Hulse-Kemp
Margaret Staton
ResearchOpen Access01 Nov 2021
Horticulture Research

Volume: 8, P: 1-16
Correlative light and electron microscopy for human brain and other biological models

We present a versatile correlative light and electron microscopy protocol for visualizing the ultrastructural details found in brain samples and for revealing previously undescribed features of neurodegenerative conditions.

Notash Shafiei
Daniel Stӓhli
Amanda J. Lewis
Protocols31 Mar 2025
Nature Protocols

Volume: 20, P: 2994-3023
Paleofloods stage a comeback

Geological and botanical archives can preserve evidence of exceptional floods going back centuries to millennia. Updated risk guidelines offer a new opportunity to apply lessons from paleoflood hydrology to judge the odds of future floods.

Scott St. George
Amanda M. Hefner
Judith Avila
Comments & Opinion16 Nov 2020
Nature Geoscience

Volume: 13, P: 766-768
The regulation of the sulfur amino acid biosynthetic pathway in Cryptococcus neoformans: the relationship of Cys3, Calcineurin, and Gpp2 phosphatases

Amanda Teixeira de Melo
Kevin Felipe Martho
Renata C. Pascon
ResearchOpen Access15 Aug 2019
Scientific Reports

Volume: 9, P: 1-19
Bacterial diversity dominates variable macrophage responses of tuberculosis patients in Tanzania

Hellen Hiza
Michaela Zwyer
Damien Portevin
ResearchOpen Access23 Apr 2024
Scientific Reports

Volume: 14, P: 1-12
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Tianyun Wang
Kendra Hoekzema
Evan E. Eichler
Amendments and CorrectionsOpen Access21 Oct 2020
Nature Communications

Volume: 11, P: 1
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Daniel R. Barnes
Matti A. Rookus
Antonis C. Antoniou
ResearchOpen Access15 Jul 2020
Genetics in Medicine

Volume: 22, P: 1653-1666
Structural and biochemical analysis reveals how ferulic acid improves catalytic efficiency of Humicola grisea xylanase

Izadora Cristina Moreira Oliveira
Aisel Valle Garay
Sonia Maria Freitas
ResearchOpen Access06 Jul 2022
Scientific Reports

Volume: 12, P: 1-22
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
Amendments and CorrectionsOpen Access15 Feb 2019
Nature Communications

Volume: 10, P: 1-4
Livestock integration into soybean systems improves long-term system stability and profits without compromising crop yields

Pedro Arthur de Albuquerque Nunes
Emilio Andrés Laca
Amélie Gaudin
ResearchOpen Access18 Jan 2021
Scientific Reports

Volume: 11, P: 1-14
Indigenous and Local Communities’ initiatives have transformative potential to guide shifts toward sustainability in South America

Empowering, reconnecting people and nature, and intercultural and ancestral education are Indigenous People and Local Community Initiatives that prioritize local tradition and show sustainable outcomes, according to a hierarchical analysis of 127 initiatives in Ecuador, Peru, and Colombia.

A. Jiménez-Aceituno
A. Burgos-Ayala
B. Martín-López
ResearchOpen Access19 Jun 2025
Communications Earth & Environment

Volume: 6, P: 1-9
Life stage impact on the human skin ecosystem: lipids and the microbial community

Martin P. Pagac
Bala Davient
Thomas L. Dawson Jr
ResearchOpen Access13 Jan 2025
npj Biofilms and Microbiomes

Volume: 11, P: 1-12
Discovery of human-like L-asparaginases with potential clinical use by directed evolution

Coraline Rigouin
Hien Anh Nguyen
Arnon Lavie
ResearchOpen Access31 Aug 2017
Scientific Reports

Volume: 7, P: 1-13
Polygenic risk modeling for prediction of epithelial ovarian cancer risk

Eileen O. Dareng
Jonathan P. Tyrer
Paul D. P. Pharoah
ResearchOpen Access14 Jan 2022
European Journal of Human Genetics

Volume: 30, P: 349-362
At-admission prediction of mortality and pulmonary embolism in an international cohort of hospitalised patients with COVID-19 using statistical and machine learning methods

Munib Mesinovic
Xin Ci Wong
David Zucman
ResearchOpen Access16 Jul 2024
Scientific Reports

Volume: 14, P: 1-43
Outbreak report of polymyxin-carbapenem-resistant Klebsiella pneumoniae causing untreatable infections evidenced by synergy tests and bacterial genomes

Marisa Zenaide Ribeiro Gomes
Elisangela Martins de Lima
Thaisa Medeiros Tozo
ResearchOpen Access17 Apr 2023
Scientific Reports

Volume: 13, P: 1-19
Multidisciplinary assessment of the Abbott BinaxNOW SARS-CoV-2 point-of-care antigen test in the context of emerging viral variants and self-administration

Jennifer K. Frediani
Joshua M. Levy
Wilbur A. Lam
ResearchOpen Access16 Jul 2021
Scientific Reports

Volume: 11, P: 1-9
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

Pamela Feliciano
Xueya Zhou
Wendy K. Chung
ResearchOpen Access23 Aug 2019
npj Genomic Medicine

Volume: 4, P: 1-14
An automatic speech analytics program for digital assessment of stress burden and psychosocial health

Amanda M. Y. Chu
Benson S. Y. Lam
Mike K. P. So
ResearchOpen Access13 Sept 2023
npj Mental Health Research

Volume: 2, P: 1-9
The deubiquitinase USP9X suppresses pancreatic ductal adenocarcinoma

An in vivo transposon screen in a pancreatic cancer model identifies frequent inactivation of Usp9x; deletion of Usp9x cooperates with Kras^G12D to accelerate rapidly pancreatic tumorigenesis in mice, validating their genetic interaction.

Pedro A. Pérez-Mancera
Alistair G. Rust
David A. Tuveson
Research29 Apr 2012
Nature

Volume: 486, P: 266-270
Alterations to the broad-spectrum formin inhibitor SMIFH2 modulate potency but not specificity

Marina Orman
Maya Landis
Christina L. Vizcarra
ResearchOpen Access08 Aug 2022
Scientific Reports

Volume: 12, P: 1-12
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

Inge M. M. Lakeman
Alexandra J. van den Broek
Marjanka K. Schmidt
ResearchOpen Access10 Jun 2021
Genetics in Medicine

Volume: 23, P: 1726-1737
Two truncating variants in FANCC and breast cancer risk

Thilo Dörk
Paolo Peterlongo
Douglas F. Easton
ResearchOpen Access29 Aug 2019
Scientific Reports

Volume: 9, P: 1-14
A multiplexed gRNA piggyBac transposon system facilitates efficient induction of CRISPRi and CRISPRa in human pluripotent stem cells

Dane Z. Hazelbaker
Amanda Beccard
Lindy E. Barrett
ResearchOpen Access20 Jan 2020
Scientific Reports

Volume: 10, P: 1-10
The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency

Nandaki Keshavan
Jose Abdenur
Shamima Rahman
Research29 Aug 2019
Genetics in Medicine

Volume: 22, P: 199-209
Clinical, behavioral, and neural measures of reward processing correlate with escitalopram response in depression: a Canadian Biomarker Integration Network in Depression (CAN-BIND-1) Report

Katharine Dunlop
Sakina J. Rizvi
Jonathan Downar
Research29 Apr 2020
Neuropsychopharmacology

Volume: 45, P: 1390-1397
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum

Siddharth Banka
Ratna Veeramachaneni
Dian Donnai
Research30 Nov 2011
European Journal of Human Genetics

Volume: 20, P: 381-388
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Lot Snijders Blok
Justine Rousseau
Philippe M. Campeau
Amendments and CorrectionsOpen Access02 May 2019
Nature Communications

Volume: 10, P: 1-4
Author Correction: Robust estimation of bacterial cell count from optical density

Jacob Beal
Natalie G. Farny
Jiajie Zhou
Amendments and CorrectionsOpen Access27 Oct 2020
Communications Biology

Volume: 3, P: 1
A primary hierarchically organized patient-derived model enables in depth interrogation of stemness driven by the coding and non-coding genome

Héléna Boutzen
Seyed Ali Madani Tonekaboni
John E. Dick
ResearchOpen Access21 Sept 2022
Leukemia

Volume: 36, P: 2690-2704
Measuring and forecasting progress in education: what about early childhood?

Linda M. Richter
Jere R. Behrman
Hirokazu Yoshikawa
ResearchOpen Access10 Sept 2021
npj Science of Learning

Volume: 6, P: 1-7
ASTCT, CIBMTR, and EBMT clinical practice recommendations for transplant and cellular therapies in mantle cell lymphoma

Pashna N. Munshi
Mehdi Hamadani
Timothy S. Fenske
Research20 Aug 2021
Bone Marrow Transplantation

Volume: 56, P: 2911-2921
Neurobehavioral phenotype of autism spectrum disorder associated with germline heterozygous mutations in PTEN

Robyn M. Busch
Siddharth Srivastava
Jennifer M. Phillips
ResearchOpen Access08 Oct 2019
Translational Psychiatry

Volume: 9, P: 1-9
Terrestriality and bacterial transfer: a comparative study of gut microbiomes in sympatric Malagasy mammals

Amanda C. Perofsky
Rebecca J. Lewis
Lauren Ancel Meyers
ResearchOpen Access14 Aug 2018
The ISME Journal

Volume: 13, P: 50-63
ISARIC-COVID-19 dataset: A Prospective, Standardized, Global Dataset of Patients Hospitalized with COVID-19

Ali Abbas
Sheryl Ann Abdukahil
Luis Felipe Reyes
ResearchOpen Access30 Jul 2022
Scientific Data

Volume: 9, P: 1-22
AI is a viable alternative to high throughput screening: a 318-target study

Izhar Wallach
Denzil Bernard
Abraham Heifets
ResearchOpen Access02 Apr 2024
Scientific Reports

Volume: 14, P: 1-16
The burden of incidental SARS-CoV-2 infections in hospitalized patients across pandemic waves in Canada

Finlay A. McAlister
Jeffrey P. Hau
Vicky Xu
ResearchOpen Access24 Apr 2023
Scientific Reports

Volume: 13, P: 1-10
Global fine-resolution data on springtail abundance and community structure

Anton M. Potapov
Ting-Wen Chen
Stefan Scheu
ResearchOpen Access03 Jan 2024
Scientific Data

Volume: 11, P: 1-14
Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk

Eileen O. Dareng
Jonathan P. Tyrer
Paul D. P. Pharoah
Amendments and CorrectionsOpen Access22 Mar 2022
European Journal of Human Genetics

Volume: 30, P: 630-631
Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases

Francis Rossignol
Marvid S. Duarte Moreno
Manuel Schiff
Reviews26 May 2021
Genetics in Medicine

Volume: 23, P: 1604-1615
Author Correction: AI is a viable alternative to high throughput screening: a 318-target study

Izhar Wallach
Denzil Bernard
Ellie Giles
Amendments and CorrectionsOpen Access16 Sept 2024
Scientific Reports

Volume: 14, P: 1-2
One is the loneliest number: genotypic matchmaking using the electronic health record

Elly Brokamp
Mary E. Koziura
Jimann Shin
Comments & Opinion06 Jul 2021
Genetics in Medicine

Volume: 23, P: 1830-1832

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