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A breakthrough in understanding the genetic ‘architecture’ of bipolar...
isbscience.org
Authors: Seth A. Ament, Szabolcs Szelinger, Gustavo Glusman, Justin Ashworth, Liping Hou, Nirmala Akula, Tatyana Shekhtman, Judith A.
New TGen test uses the unique genetics of women to uncover neurologic...
medicalxpress.com
TGen Research Associate Szabolcs Szelinger, the paper's lead author, said: "With just a small bio sample, we are now able to provide a ...
TGen News & Press Releases : New test developed at TGen uses the...
www.tgen.org
TGen Research Associate Szabolcs Szelinger, an Arizona State University graduate student in Molecular and Cellular Biology and the paper's ...
Telephone & Addresses
Szabolcs Szelinger
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View phone numbers, addresses, public records, background check reports and possible arrest records for Szabolcs Szelinger. Whitepages people search is ...
WhitePages: Szelinger | Whitepages
Szabolcs Szelinger. Age:40-44; Current:Phoenix, AZ. Prior:Chandler AZ, Fresh Meadows NY; Knows:Tibor S Szelinger. View Full ProfileView More Details.
People directory - Last Names - Szelinger
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Szabolcs Szelinger . 1,379,043,021 total records available. Tweet. Testimonials Read testimonials from real customers who already used our services. Read More.
Network Profiles
Interests
Gene causing appearance of premature aging found: Gene also appears...
www.sciencedaily.com
A genetic mutation associated with the appearance of premature aging and severe loss of body fat in children has been identified by scientists. They found that...
Identification of a Novel Risk Locus for Progressive Cell
www.cell.com
Szabolcs Szelinger. x. Szabolcs Szelinger. Search for articles by this author ...
Mutated gene is likely cause of 3-year-old girl's severe disorder:...
www.sciencedaily.com
A young girl with severe neurological symptoms finally has a diagnosis, following the discovery of a genetic mutation that likely caused the girl to experience...
New test uses unique genetics of women to uncover neurologic...
www.sciencedaily.com
A discovery relies on a simple genetic fact: Men have one X and one Y chromosome, while women have two X chromosomes. This women-only factor was leveraged by...
Business Profiles
Researchgate: Szabolcs Szelinger
Phoenix, AZ, United States
Education
Genome-wide significant association between a 'negative mood...
kclpure.kcl.ac.uk
... Peter P Zandi ; Pamela B Mahon ; Melvin Mcinnis ; David Craig; Szabolcs Szelinger ; M M N??then ; S Cichon ; T G Schulze ; M Rietschel ...
Genome-wide significant association between a 'negative mood...
kclpure.kcl.ac.uk
... and Mahon, {Pamela B} and Melvin Mcinnis and David Craig and Szabolcs Szelinger and N??then, {M M} and S Cichon and Schulze, {T G} and M Rietschel",.
Projects
Addition of RG:Z tags - SourceForgesourceforge.net › samtools › mailman › attachment
sourceforge.net
Szabolcs Szelinger Research Associate, Neurobehavioral Research Unit Neurogenomics Division, The Translational Genomics Research Institute (TGen)
SAM tools / Re: [Samtools-help] Addition of RG:Z tags
sourceforge.net
:32:41 BST > To: Szabolcs Szelinger <sszelinger@...> > Subject: Re: ...
SAM tools / Re: [Samtools-help] BAM to MAQ SNP caller
sourceforge.net
Heng On Fri, Sep 04, at 03:34:39PM , Szabolcs Szelinger wrote: > Hi all, > I have .bam files calibrated by GenomeAnalysis tool kit, and used BWA for ...
SAM tools / [Samtools-devel] 2. Re: pileup with too many reads
sourceforge.net
From: Szabolcs Szelinger <sszelinger@tg...> :12:59. On Feb 5, 2010, at 7:39 AM, samtools-devel- request@... wrote: > 2.
Books & Literature
Szabolcs Szelinger author profile – Rxivistrxivist.org › authors
rxivist.org
Research profile for Szabolcs Szelinger (The Translational Genomics Research Institute), provided by Rxivist, the site that helps you find the most discussed ...
Search Results
molecularcasestudies.cshlp.org
An open-access, peer-reviewed, international journal in the field of precision medicine. Articles in the journal present genomic and molecular analyses of...
(K)information: Gamete Donation and Kinship Knowledge in ...books.google.com › books
books.google.de
Social Science and Medicine, 70, 1867– Homer, Nils, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, et al. (2008).
Human Subjects Research Regulation: Perspectives on the Future -...
books.google.de
Science 18: 321–24. Harmon, Amy Indian tribe wins fight to limit research of Its DNA. New York Times, April 21. Accessed October 17, http://www.nytimes .com us/22dna.html?pagewanted=all&_r=0. Homer, Nils, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, ...
Related Documents
CiteSeerX — Chapter 4 Microarray-Based Genome-Wide Association...
citeseerx.ist.psu.edu
Chapter 4 Microarray-Based Genome-Wide Association Studies Using Pooled DNA {Szabolcs Szelinger and ... {Chapter 4 Microarray-Based Genome-Wide Association ...
A novel variant in TAF1 affects gene expression and is ...www.scienceopen.com › document
www.scienceopen.com
Authors: Sarah E. Hurst , Erika Liktor-Busa , Aubin Moutal , Sara Parker , Sydney Rice , Szabolcs Szelinger , Grant Senner , Michael F. Hammer ...
CiteSeerX — Resolving Individuals Contributing Trace Amounts of DNA...
citeseerx.ist.psu.edu
Resolving Individuals Contributing Trace Amounts of DNA to ... and Szabolcs Szelinger and Margot ... Individuals Contributing Trace Amounts of DNA to ...
Scientific Publications
A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized...
www.sciencedirect.com
... Joshua Deignan, Fabiola Quintero-Rivera, Sibel Kantarci, Naghmeh Dorrani, Sureni Mullegama, Sung-Hae Kang, and Szabolcs Szelinger.
A De Novo Mutation in TEAD1 Causes Non-X-Linked Aicardi ...pubmed.ncbi.nlm.nih.gov › ...
pubmed.ncbi.nlm.nih.gov
Isabelle Schrauwen , Szabolcs Szelinger , Ashley L Siniard , Jason J Corneveaux , Ahmet Kurdoglu , Ryan Richholt , Matt De Both , Ivana Malenica , Shanker ...
Challenges of web-based personal genomic data sharing | Life...
lsspjournal.biomedcentral.com
Google Scholar; Homer, Nils, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, John V. Pearson, Dietrich A.
Publications
Microarray-Based Genome-Wide Association Studies Using Pooled DNA |...
link.springer.com
Szabolcs Szelinger Affiliated with Neurogenomics Division, Translational Genomics Research Institute, John V. Pearson Affiliated with Neurogenomics Division ...
Oalib search
www.oalib.com
Search Results: of 53 matches for " Szabolcs Szelinger " All listed articles are free for downloading (OA Articles) ...
Reports & Statements
Identification of genetic variants using bar-coded multiplexed...
www.nature.com
Targeted regions of the human genome are resequenced in multiplex with Illumina technology, and the pipeline is evaluated for polymorphism discovery and...
Biomarker Roundup No. 6
www.ispecimen.com
Researchers found biomarkers and proteins pertinent to intracranial lesions, X-chromosome-linked diseases, obesity, and nanomedicine.
Identification of genetic variants using bar-coded Naturewww.nature.com › nature › nature methods › articles
www.nature.com
David W Craig,; John V Pearson,; Szabolcs Szelinger,; Aswin Sekar ,; Margot Redman ,; Jason J Corneveaux ,; Traci L Pawlowski ,; Trisha ...
CurePSP • View topic - racial/ethnic background and PSP - CurePSP ...
forum.curepsp.org
... John V. Pearson, Matt Baker, Victoria L. Zismann, Jennifer Gass, Jennifer Adamson, Szabolcs Szelinger, Jason Corneveaux, Ashley Cannon, ...
Miscellaneous
Szabolcs Szelinger | LinkedIn
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View Szabolcs Szelinger's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Szabolcs Szelinger ...
Szabolcs Szelinger | ACMG Annual Clinical Genetics Meeting ...epostersonline.com › acmg2017 › node
epostersonline.com
Poster Presenter: Szabolcs Szelinger. Select rating, Give it 1/5, Give it 2/5, Give it 3/5, Give it 4/5, Give it 5/5, Cancel rating. Cancel rating. Give it Give it 2/5.
Dementia: Szelinger, Szabolcs - Expertscape.com
expertscape.com
Szabolcs Szelinger has special expertise in Dementia
Szabolcs Szelinger Results at Athlinks.com
alaska.athlinks.com
Szabolcs Szelinger Results at Athlinks.com.
"Efficient region-based test strategy uncovers genetic risk ...digitalcommons.psjhealth.org › publications
digitalcommons.psjhealth.org
Szabolcs Szelinger · Jens Treutlein · Stephanie H Witt · Peter P Zandi · Peng Zhang · Sebastian Zöllner · Heike Bickeböller · Peter G Falkai
A Frame-Shift Mutation in CAV1 Is Associated with a Severe ...figshare.com › collections › Expression_heatmaps_of_RN...
figshare.com
Szabolcs Szelinger. Ashley L. Siniard. Ahmet Kurdoglu. Jason J. Corneveaux. Ivana Malenica. Ryan Richholt. Guy Van Camp. Matt De Both.
3655 W Elgin St Chandler Az Address Search Results
www.fastpeoplesearch.com
Used to live: Phoenix, AZ, Flushing, NY, Glendale, AZ, Chandler, AZ, Fresh Meadows, NY. AKA: Sean Szelinger , Szabolcs Szelinger , Szabolos Szelinger , Mr ...
Altmetric – Genome-wide association study of 40,000 individuals...
www.altmetric.com
... Nicholas J. Schork, Thomas G. Schulze, Johannes Schumacher, Barbara W. Schweizer, Giovanni Severino, Tatyana Shekhtman, Paul D. Shilling, Christian Simhandl, Claire M. Slaney, Erin N. Smith, Alessio Squassina, Thomas Stamm, Pavla Stopkova, Fabian Streit, Jana Strohmaier, Szabolcs Szelinger, Sarah K. Tighe, ...
Article Usage Statistics Center - Molecular Case Studiesmolecularcasestudies.cshlp.org › articleusage
molecularcasestudies.cshlp.org
Abby M Moskowitz,; Newell Belnap,; Ashley L Siniard,; Szabolcs Szelinger,; Ana M Claasen,; Ryan F Richholt,; Matt De Both,; Jason J Corneveaux,; Chris Balak, ...
Case Report: Compound heterozygous nonsense... | F1000Research
f1000research.com
Read the original article in full on F1000Research: Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed...
A Syndromic Intellectual Disability Disorder Caused by Variants in...
jhu.pure.elsevier.com
Jing You ; Nara L. Sobreira ; Dustin L. Gable ; Julie Jurgens ; Dorothy K. Grange ; Newell Belnap ; Ashley Siniard ; Szabolcs Szelinger ; Isabelle Schrauwen ...
Articles from collection Rare diseases - F1000Researchf1000research.com › Collections
f1000research.com
Erika Banuelos, Keri Ramsey, Newell Belnap, Malavika Krishnan, Chris D. Balak, Szabolcs Szelinger, Ashley L. Siniard, Megan Russell, Ryan Richholt, Matt De ...
Cancer/Oncology - AMP2017
amp17.amp.org
Szabolcs Szelinger, PhD, University of California, Los Angeles, CA, USA. H34 - Implementation Considerations: Designing and Medically ...
Altmetric – Identification of genetic variants using bar-coded...
www.altmetric.com
... Huentelman MJ, David W Craig, John V Pearson, Szabolcs Szelinger, Aswin Sekar, Margot Redman, Jason J Corneveaux, Traci L Pawlowski, Trisha Laub, ...
Articles from collection Rare diseases - F1000Research
f1000research.com
Read the latest peer reviewed Rare diseases articles and more on F1000Research
Collaboration matters when looking for answers to undiagnosed...
blogs.bcm.edu
Other contributors of this work include Kelly Schoch, Szabolcs Szelinger, David R. Bearden, Asbjorg Stray-Pedersen, Oyvind L. Busk, Nicholas Stong, Eriskay Liston, Ronald D. Cohn, Fernando Scaglia, Jill A. Rosenfeld, Jennifer Tarpinian, Cara M. Skraban, Matthew A. Deardorff, Jeremy N. Friedman, ...
Exploring genome-wide DNA methylation patterns in Aicardi ...read.qxmd.com › read › exploring-genome-wide-dna-...
read.qxmd.com
... Newell Belnap, Chris D Balak, Wayne M Jepsen, Szabolcs Szelinger, Ashley L Siniard, Candace R Lewis, Madison LaFleur, Ryan F Richholt, Matt D De Both, ...
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