Matt Parker
Director, Clinical Bioinformatics Software at Oxford Nanopore in the EPI2ME team. Interested in regulated application of Nanopore sequencing. Also bikes, beers, trains, and the American Office.
@hkilpinen.bsky.social
Assistant Professor in Genome Biology @HiLIFE_helsinki, @FIMM_UH, @UH_Neuro and @BioEnvHelsinki. Stem cells, single cells, genomics, and neurodevelopment.
@mehurles.bsky.social
Director, Wellcome Sanger Institute. Decipherer of developmental disorders. Co-founder Congenica. Dad, husband, cyclist, gardener. Views own.
@hcmefford.bsky.social
Physician scientist @ St. Jude (neuro)genetics | genomics epilepsy | rare disease | precision medicine
@philippamay.bsky.social
Consultant Clinical Scientist in Genomics. Talk to me about paediatric cancer, cardiovascular and respiratory disease, telomeres..... Veggie Londoner with a fondness for Ireland, halloumi, chocolate orange Twirls and wildlife. Easily startled.
@rachelbuc.bsky.social
Cardiovascular genetic scientist, crafter, mum. Passionate about opening up cardiovascular research to more people - @thehearthive.bsky.social. Has too many hobbies. London, UK
@jamesware.bsky.social
Clinician Scientist. Cardiovascular genetics, genomics in healthcare, inherited cardiac conditions, open science, patient participation. He/him. https://profiles.imperial.ac.uk/j.ware
@drjennylord.bsky.social
Lecturer in Systems Biology at the University of Sheffield. Interested in bioinformatics, RNA, splicing, big data, rare disease diagnostics and neuroscience. Also dogs.
@agoriely.bsky.social
Human genetics, rare disease and de novo variant detection | selfish selection | mosaicism | cell competition | paternal age effects | spermatogenesis | testis @University of Oxford @MRC- WIMM
@chundru.bsky.social
Postdoc University of Exeter 🇮🇪🇮🇳🇬🇧 Integrating 'omics data into rare variant genetic analyses Formerly at Sanger institute working on recessive developmental disorders in DDD
@emiliewigdor.bsky.social
Postdoc in neurogenetics | Sanders Lab at University of Oxford and IDRM | JRF at the Centre for Personalised Medicine
@htanudisastro.bsky.social
MD-PhD candidate at the University of Sydney & Garvan Institute. Studying tandem repeats in single-cell contexts w/ @dgmacarthur.bsky.social
@carolinefwright.bsky.social
Academic research scientist in human genetics and genomic medicine; pianist & composer; hiker & outdoors enthusiast.
@svergult.bsky.social
PI of the Functional Genomics lab (https://fungenlab-ugent.be/) at Ghent University. Elucidating the genetics of neurodevelopmental disorders. Special interest in the role of the non-coding genome during neurodevelopment.
@christeldepienne.bsky.social
Molecular geneticist | Neurogenetics | repeat expansions | chromosome X | snRNAs | and more
@poseypod.bsky.social
Physician-scientist, Adult genetics, Human genetics research, Baylor College of Medicine. Thoughts expressed = my own.
@eedhaene.bsky.social
postdoc @ http://debaerelab.com @ https://fungenlab-ugent.be | 3D genome, gene regulation, structural variation | retina, neurodev, space!
@ginaravenscroft.bsky.social
Rare & neuromuscular disease researcher at UWA & the Harry Perkins Institute, Perth 🇦🇺 Passionate about #sciencefunding, #womeninSTEM, #EMCRs Mum of 👦👧🐶 Posting about genomics, rare disease, PI life & wine https://www.ravenscroftlab.com
@gc4gc.bsky.social
rare disease neurogeneticist | epilepsy | epigenetics | iPSCs | mentor & genetics MedEd | here for the science, lab fun & occasionally my tiny hooman https://sites.northwestern.edu/carvilllab/
@smcgrath.phd
Biomedical Informatics PhD • CITRIS Health @UC Berkeley • FAMIA • Focusing on Informatics and AI in medicine • Missoula MT https://citris-uc.org/people/person/scott-mcgrath/
@hannahlong.bsky.social
Group Leader @mrc_hgu investigating gene regulation in development & human disease
@zornitza.bsky.social
Clinical Lead, Australian Genomics. Clinical Geneticist, VCGS. Professor, University of Melbourne. Rare disease genomics. 🧬🇦🇺
@sebatlab.bsky.social
Psychiatric genetics, complex trait genetics, genome sequencing, rare variants are my jam
@jonnyfrazer.bsky.social
Probabilistic machine learning to address questions in evolution and health #EvolutionaryMedicine. PI at the Centre for Genomic Regulation, co-leading a group with Mafalda Dias. Previously Harvard.
@danrdanny.bsky.social
CODA. Dad. Interested in genetics, long-read sequencing, and ultramarathon running. Assistant Professor at University of Washington. The command line is my happy place. https://millerlaboratory.com
@jorisveltman.bsky.social
Happy European human geneticist enjoying life in the United Kingdom. Love everything genomics, even married a genomicist..;)
@polona.bsky.social
DVM PhD | Researcher at the University of Auckland | Genomics, variant interpretation | Rare diseases | Cancer, Molecular Tumour Boards | Inherited cardiac diseases | 🧬
@jacobvorstman.bsky.social
Professor of Psychiatry at The Hospital for Sick Children / University of Toronto. Editor in Chief of the Journal of Neurodevelopmental Disorders. Neurodevelopment, (Child) Psychiatry, Genetics, The Music of Life,
@ruebenadawes.bsky.social
Sydney girl, Fulbright recipient 2020-2021 with Monkol Lek. PhD Kids Research Sydney 2022, now postdoc with @nickywhiffin.bsky.social at BDI Oxford. Splicing & smORFs!
@ahoischen.bsky.social
Genomic technologies: WES/WGS, long-read sequencing, optical genome mapping, somatic mutations; Immuno-genomics: rare diseases; immunodeficiencies; inborn errors of immunity; clonal hematopoiesis https://shorturl.at/MxQ7O https://www.immuno-genomics.com
@inaklockner.bsky.social
Postdoc exploring new gene editing therapies for the neurodevelopmental disorder #AngelmanSyndrome at #UNCZylkaLab, also interested in post-transcriptional gene regulation via non-coding RNAs in neuromuscular disease |she/her|🇩🇪 🇺🇲
@profsimonfisher.bsky.social
Director of Language & Genetics at Max Planck Institute, Nijmegen. Tracing the complex connections between genes, brains, speech & language. Website: https://www.mpi.nl/people/fisher-simon-e ORCID: https://orcid.org/0000-0002-3132-1996
@rikkesmoller.bsky.social
Geneticist/Professor at the Danish Epilepsy Centre, Filadelfia & University of Southern Denmark 🇩🇰 I Epilepsy 💜 | Precision Medicine 💊 I Genetics 🧬 | Rare Disease 🦓 |
@hheyne.bsky.social
Research group leader at Hasso Plattner Institute. Medical genomics, precision medicine, epilepsy.
@jonroberts.bsky.social
Research genetic counsellor. PhD in Science Communication. Researching equitable genomic testing & genetics of neurdevelopmental disorders. https://substack.com/@jonathanrob1985?utm_source=user-menu
@alucassen.bsky.social
Prof Genomic Medicine, UoOxford Director Centre for Personalised Medicine https://cpm.ox.ac.uk/ Interested in how we bring together ethics, social, molecular and clinical sciences to make sense of genomics. @annekeluc at the other place
@tatyanes.bsky.social
Genetic counsellor at Queensland Children’s Hospital and Research Fellow at Integrating Genomics into Medicine Group, The University of Queensland; she/her 🇦🇺🇧🇷 #genechat https://www.igmgenomics.com
@marion-mam.bsky.social
Clinical Geneticist in Toulouse 🧬 Passionate about rare diseases and skeletal disorders 🔥
@franziskaauer.bsky.social
Group Leader at Technical University Munich, Germany. Focus on 🧪 childhood cancer predisposition / leukemia / prevention / genetics / genomics 🧬
@jdbux.bsky.social
Director, Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai. Shakuhachi student.
@plasmidsaurus.bsky.social
Sequence plasmids, amplicons, colonies, AAV, yeast, and bacterial genomes! Our advanced sequencing delivers comprehensive visibility, higher accuracy, and the ability to detect structural variations and rare mutations that other sequencing methods miss.
@erictopol.bsky.social
physician-scientist, author, editor https://www.scripps.edu/faculty/topol/ Ground Truths https://erictopol.substack.com SUPER AGERS https://www.simonandschuster.com/books/Super-Agers/Eric-Topol/9781668067666
@magdalenaskipper.bsky.social
Editor in Chief of Nature, geneticist, editor, accidental potter. All views my own