Faculty

Institution

Unit

Venue

Lynn B. Jorde

University of Utah

Affiliations

Spencer Fox Eccles School of Medicine

Human Genetics

NoneLynn B. Jorde is currently serving as a Human Genetics faculty at University of Utah.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Lynn B. Jorde

University of Utah

You can click a keyword to filter the displayed items

genetics human genetics genomics population genetics molecular biology medical genetics evolutionary biology genome biology anthropology molecular genetics human evolution hematology human biology population genomics gene expression physical anthropology cytogenetics genetic disorders evolutionary genetics genome analysis obstetrics and gynaecology heredity developmental genetics preterm birth genetic structure adaptation chromosome biology natural selection cancer genetics regional studies linkage disequilibrium population history blood pressure human variation host genetics genome sequencing avian biology genetic diversity paleoanthropology next-generation sequencing genetic basis utah mormons genetic evidence vascular biology mutagenesis human polymorphisms juvenile idiopathic arthritis neural tube defects whole-genome sequencing mammalian biology respiratory medicine arthritis cardiovascular research circulatory physiology thrombosis reproductive biology tibetan plateau gene evolution endocrine research sequence analysis genomic medicine high-altitude adaptation comprehensive analysis genetic disease nature genetic counseling immunogenetics disease gene identification immune-related gene polymorphism ulnar-mammary syndrome demographic history human populations alu elements dna sequence variation human genomic diversity migration matrices epidemiology human genetic variation human genome genetic epidemiology genetic variation

Notable Scholarly Works

Notable Federal Grants

Collaborators

A Familial, Telomere-To-Telomere Reference for Human De Novo Mutation and Recombination From a Four-Generation Pedigree. bioRxiv (Cold Spring Harbor Laboratory) (2024)

David PorubskyHarriet DashnowThomas A. SasaniGlennis A. LogsdonPille HallastMichelle D. NoyesZev N. KronenbergTom MokveldNidhi KoundinyaCillian NolanCody J. SteelyAndrea GuarracinoEgor DolzhenkoWilliam T. HarveyWilliam J. RowellKirill GrigorevThomas J. NicholasKeisuke K. OshimaJiadong LinPeter EbertW. Scott WatkinsTiffany Y. LeungVincent C.T. HanlonSean McGeeBrent S. PedersenMichael E. GoldbergHannah C. HappHyeonsoo JeongKatherine M. MunsonKendra HoekzemaDaniel D. ChanYanni WangJordan KnuthGage H. GarciaCairbre FanslowChristine LambertCharles LeeJoshua D. SmithShawn LevyChristopher E. MasonErik GarrisonPeter M. LansdorpDeborah W. NeklasonLynn B. JordeAaron R. QuinlanMichael A. EberleEvan E. Eichler

genomicsgenetic recombinationgenetic basisgeneticsfour-generation pedigreemolecular biologymolecular geneticstelomere-to-telomere referencehuman geneticsevolutionary biology

Genetic Resonance: Dissecting the Heritability and Genetic Correlations of Human Hearing Acuity. G3 Genes Genomes Genetics (2024)

Jerry A DuranW Scott WatkinsDeborah W NeklasonLynn B Jorde

genomicsheredityhuman hearinggenetic basisgeneticsbiologygenetic variationhuman hearing acuitygenetic resonancemolecular biologymolecular geneticshearing researchgenetic correlationshuman geneticspopulation genetics

Inherited Genetic Risk in Stillbirth: A Shared Genomic Segments Analysis of High-Risk Pedigrees.. Research Square (Research Square) (2024)

Tsegaselassie WorkalemahuMyke MadsenSarah LopezJessica PageNathan BlueCecile AveryRob SargentZhe YuEmily GuintoD Ware BranchSusannah LeisherLynn JordeAaron QuinlanHilary CoonMichael VarnerClaire RobertsDeborah NeklasonNicola CampRobert Silver

public healthgenomicsgenetic factorshereditygenomic segments analysisgenetic predispositionepidemiologygenetic basisgeneticshigh-risk pedigreesmedical geneticsgenetic epidemiologyhuman geneticsgenetic disorderspopulation geneticsgenetic risk

Mapping Genetic Susceptibility to Preterm Birth: Analysis of Utah Pedigrees Using Shared Genomic Segment Analysis. Research Square (Research Square) (2024)

Tsegaselassie WorkalemahuErin A. S. ClarkMichael J. MadsenZhe YuSusan E. DaltonSean M. EsplinTracy ManuckDeborah NeklasonWilfred Chen-Han WuLynn B. JordeNicola J CampRobert M SilverMichael W Varner

public healthgenomicsgenetic susceptibilitygenomic segment analysispreterm birthepidemiologygenetic predispositiongeneticsutah pedigreesgenetic epidemiologyhuman geneticspopulation genetics

Mapping Genetic Susceptibility to Spontaneous Preterm Birth: Analysis of Utah Pedigrees to Find Inherited Genetic Factors. American Journal of Obstetrics and Gynecology (2024)

Tsegaselassie WorkalemahuErin A S ClarkMichael J MadsenZhe YuSusan E DaltonM Sean EsplinTracy ManuckDeborah NeklasonChen-Han Wilfred WuLynn B JordeNicola J CampRobert M SilverMichael W Varner

genetic factorsgenetic susceptibilitypreterm birthgenetic predispositioninherited genetic factorsgeneticsspontaneous preterm birthobstetrics and gynaecologydisease susceptibilitygenetic epidemiology

Shared Genomic Segments Analysis Identifies Mhc Class I and Class III Molecules as Genetic Risk Factors for Juvenile Idiopathic Arthritis. Human Genetics and Genomics Advances (2024)

Cecile N AveryNicole D RussellCody J SteelyAimee O HershJohn F BohnsackSampath PrahaladLynn B Jorde

genomicsjuvenile idiopathic arthritisgenetic predispositiongeneticsgenetic risk factorshuman genetics

The Platinum Pedigree: A Long-Read Benchmark for Genetic Variants. bioRxiv (Cold Spring Harbor Laboratory) (2024)

Zev KronenbergCillian NolanTom MokveldWilliam J RowellSangjin LeeEgor DolzhenkoPi-Chuan ChangJames Matthew HoltChristopher T SaundersNathanael D. OlsonSean McGeeAndrea GuarracinoNidhi KoundinyaWilliam T HarveyW. Scott WatkinsKatherine M MunsonKendra HoekzemaKhi Pin ChuaCairbre FanslowChristine LambertHarriet DashnowErik GarrisonJosh SmithPeter LansdorpJustin M ZookAndrew CarrollLynn B. JordeDeborah W NeklasonAaron QuinlanEvan EichlerMichael A Eberle

genomicslong-read benchmarkgeneticsgenetic variationmolecular biologymolecular geneticsgenetic variantsplatinum pedigreehuman geneticspopulation genomicspopulation geneticsgenotype-phenotype association

Characterizing Genetic Variation in the Regulation of the Er Stress Response Through Computational and Cis -Eqtl Analyses. G3 Genes Genomes Genetics (2023)

Nikki D RussellLynn B JordeClement Y Chow

physiologygenomicser stress responsehuman geneticsgeneticsgenetic variationgenetic analysisgene characterizationstatistical geneticsneurosciencequantitative genetics

Whole-Genome Sequencing Analysis in Families With Recurrent Pregnancy Loss: A Pilot Study. PLoS ONE (2023)

Tsegaselassie WorkalemahuCecile AverySarah LopezNathan R. BlueAmelia WallaceAaron R. QuinlanHilary CoonDerek WarnerMichael W. VarnerD. Ware BranchLynn B. JordeRobert M. Silver

genomicsgenome biologypregnancy lossvariant interpretationhereditynext-generation sequencinghuman geneticsgenomic medicinerecurrent pregnancy lossgeneticspilot wgs studyobstetrics and gynaecologymolecular diagnosticsreproductive healthgenetic epidemiologygynecology

Familial Aggregation of Stillbirth: A Pedigree Analysis of a Matched Case–Control Study. BJOG An International Journal of Obstetrics & Gynaecology (2022)

Tsegaselassie WorkalemahuJessica M. PageHuong MeeksZhe YuEmily GuintoAlison FraserMichael W. VarnerLauren H. TheilenAaron QuinlanHilary CoonDaniel A. EnquobahrieCande V. AnanthFasil Tekola‐AyeleLynn B. JordeRobert M. Silver

familial aggregationepidemiologysurvival analysispsychologycase-control studybiostatisticspedigree analysis

1
2
3
4
5
30
10 / page

Lynn B. Jorde

University of Utah

Affiliations

Spencer Fox Eccles School of Medicine

Human Genetics

NoneLynn B. Jorde is currently serving as a Human Genetics faculty at University of Utah.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Lynn B. Jorde

University of Utah

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

A Familial, Telomere-To-Telomere Reference for Human De Novo Mutation and Recombination From a Four-Generation Pedigree. bioRxiv (Cold Spring Harbor Laboratory) (2024)

genomicsgenetic recombinationgenetic basisgeneticsfour-generation pedigreemolecular biologymolecular geneticstelomere-to-telomere referencehuman geneticsevolutionary biology

Genetic Resonance: Dissecting the Heritability and Genetic Correlations of Human Hearing Acuity. G3 Genes Genomes Genetics (2024)

Jerry A DuranW Scott WatkinsDeborah W NeklasonLynn B Jorde

Inherited Genetic Risk in Stillbirth: A Shared Genomic Segments Analysis of High-Risk Pedigrees.. Research Square (Research Square) (2024)

Mapping Genetic Susceptibility to Preterm Birth: Analysis of Utah Pedigrees Using Shared Genomic Segment Analysis. Research Square (Research Square) (2024)

Tsegaselassie WorkalemahuErin A. S. ClarkMichael J. MadsenZhe YuSusan E. DaltonSean M. EsplinTracy ManuckDeborah NeklasonWilfred Chen-Han WuLynn B. JordeNicola J CampRobert M SilverMichael W Varner

public healthgenomicsgenetic susceptibilitygenomic segment analysispreterm birthepidemiologygenetic predispositiongeneticsutah pedigreesgenetic epidemiologyhuman geneticspopulation genetics

Mapping Genetic Susceptibility to Spontaneous Preterm Birth: Analysis of Utah Pedigrees to Find Inherited Genetic Factors. American Journal of Obstetrics and Gynecology (2024)

Tsegaselassie WorkalemahuErin A S ClarkMichael J MadsenZhe YuSusan E DaltonM Sean EsplinTracy ManuckDeborah NeklasonChen-Han Wilfred WuLynn B JordeNicola J CampRobert M SilverMichael W Varner

genetic factorsgenetic susceptibilitypreterm birthgenetic predispositioninherited genetic factorsgeneticsspontaneous preterm birthobstetrics and gynaecologydisease susceptibilitygenetic epidemiology

Shared Genomic Segments Analysis Identifies Mhc Class I and Class III Molecules as Genetic Risk Factors for Juvenile Idiopathic Arthritis. Human Genetics and Genomics Advances (2024)

Cecile N AveryNicole D RussellCody J SteelyAimee O HershJohn F BohnsackSampath PrahaladLynn B Jorde

genomicsjuvenile idiopathic arthritisgenetic predispositiongeneticsgenetic risk factorshuman genetics

The Platinum Pedigree: A Long-Read Benchmark for Genetic Variants. bioRxiv (Cold Spring Harbor Laboratory) (2024)

Characterizing Genetic Variation in the Regulation of the Er Stress Response Through Computational and Cis -Eqtl Analyses. G3 Genes Genomes Genetics (2023)

Nikki D RussellLynn B JordeClement Y Chow

physiologygenomicser stress responsehuman geneticsgeneticsgenetic variationgenetic analysisgene characterizationstatistical geneticsneurosciencequantitative genetics

Whole-Genome Sequencing Analysis in Families With Recurrent Pregnancy Loss: A Pilot Study. PLoS ONE (2023)

Tsegaselassie WorkalemahuCecile AverySarah LopezNathan R. BlueAmelia WallaceAaron R. QuinlanHilary CoonDerek WarnerMichael W. VarnerD. Ware BranchLynn B. JordeRobert M. Silver

Familial Aggregation of Stillbirth: A Pedigree Analysis of a Matched Case–Control Study. BJOG An International Journal of Obstetrics & Gynaecology (2022)

familial aggregationepidemiologysurvival analysispsychologycase-control studybiostatisticspedigree analysis

1
2
3
4
5
30
10 / page

Similar Faculty Members

David Valle

Institution

Johns Hopkins University

genetics

human genetics

Aravinda Chakravarti

Institution

New York University

genetic epidemiology

genomic medicine

Mark Yandell

Institution

University of Utah

genome analysis

genomics

Kenneth Kidd

Institution

Yale University

human genetics

heredity

Steven Hunt

Institution

University of Utah

health science

preventive cardiology

Gary M. Shaw

Institution

Stanford University

maternal-fetal medicine

infertility

Carlos Bustamante

Institution

Stanford University

genetics

genomics

Scott Williams

Institution

Case Western Reserve University

human genetics

health science

Joel Naom Hirschhorn

Institution

Harvard University

reproductive biology

human genetics

Michael Province, PhD

Institution

Washington University in St. Louis

gene discovery

pharmacogenomics

Similar Faculty Members

David Valle

Institution

Johns Hopkins University

genetics

human genetics

Aravinda Chakravarti

Institution

New York University

genetic epidemiology

genomic medicine

Mark Yandell

Institution

University of Utah

genome analysis

genomics

Kenneth Kidd

Institution

Yale University

human genetics

heredity

Steven Hunt

Institution

University of Utah

health science

preventive cardiology

Gary M. Shaw

Institution

Stanford University

maternal-fetal medicine

infertility

Carlos Bustamante

Institution

Stanford University

genetics

genomics

Scott Williams

Institution

Case Western Reserve University

human genetics

health science

Joel Naom Hirschhorn

Institution

Harvard University

reproductive biology

human genetics

Michael Province, PhD

Institution

Washington University in St. Louis

gene discovery

pharmacogenomics