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  1. Article ; Online: Gene and pathway based burden analyses in familial lymphoid cancer cases: Rare variants in immune pathway genes.

    Ralli, Sneha / Jones, Samantha J / Leach, Stephen / Lynch, Henry T / Brooks-Wilson, Angela R

    PloS one

    2023  Volume 18, Issue 6, Page(s) e0287602

    Abstract: Genome-wide association studies have revealed common genetic variants with small effect sizes associated with diverse lymphoid cancers. Family studies have uncovered rare variants with high effect sizes. However, these variants explain only a portion of ... ...

    Abstract Genome-wide association studies have revealed common genetic variants with small effect sizes associated with diverse lymphoid cancers. Family studies have uncovered rare variants with high effect sizes. However, these variants explain only a portion of the heritability of these cancers. Some of the missing heritability may be attributable to rare variants with small effect sizes. We aim to identify rare germline variants associated with familial lymphoid cancers using exome sequencing. One case per family was selected from 39 lymphoid cancer families based on early onset of disease or rarity of subtype. Control data was from Non-Finnish Europeans in gnomAD exomes (N = 56,885) or ExAC (N = 33,370). Gene and pathway-based burden tests for rare variants were performed using TRAPD. Five putatively pathogenic germline variants were found in four genes: INTU, PEX7, EHHADH, and ASXL1. Pathway-based association tests identified the innate and adaptive immune systems, peroxisomal pathway and olfactory receptor pathway as associated with lymphoid cancers in familial cases. Our results suggest that rare inherited defects in the genes involved in immune system and peroxisomal pathway may predispose individuals to lymphoid cancers.
    MeSH term(s) Humans ; Genome-Wide Association Study ; Genetic Predisposition to Disease ; Neoplasms ; Germ-Line Mutation ; Exome Sequencing
    Language English
    Publishing date 2023-06-28
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0287602
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Simulating pedigrees ascertained for multiple disease-affected relatives.

    Nieuwoudt, Christina / Jones, Samantha J / Brooks-Wilson, Angela / Graham, Jinko

    Source code for biology and medicine

    2018  Volume 13, Page(s) 2

    Abstract: Background: Studies that ascertain families containing multiple relatives affected by disease can be useful for identification of causal, rare variants from next-generation sequencing data.: Results: We present the R package SimRVPedigree, which ... ...

    Abstract Background: Studies that ascertain families containing multiple relatives affected by disease can be useful for identification of causal, rare variants from next-generation sequencing data.
    Results: We present the R package SimRVPedigree, which allows researchers to simulate pedigrees ascertained on the basis of multiple, affected relatives. By incorporating the ascertainment process in the simulation, SimRVPedigree allows researchers to better understand the within-family patterns of relationship amongst affected individuals and ages of disease onset.
    Conclusions: Through simulation, we show that affected members of a family segregating a rare disease variant tend to be more numerous and cluster in relationships more closely than those for sporadic disease. We also show that the family ascertainment process can lead to apparent anticipation in the age of onset. Finally, we use simulation to gain insight into the limit on the proportion of ascertained families segregating a causal variant. SimRVPedigree should be useful to investigators seeking insight into the family-based study design through simulation.
    Language English
    Publishing date 2018-10-15
    Publishing country England
    Document type Journal Article
    ZDB-ID 2254831-2
    ISSN 1751-0473
    ISSN 1751-0473
    DOI 10.1186/s13029-018-0069-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Birth Order, Sibship Size, Childhood Environment and Immune-Related Disorders, and Risk of Lymphoma in Lymphoid Cancer Families.

    Jones, Samantha J / Stroshein, Sumara / Williams, Amy M / Liu, Dongmeng / Spinelli, John J / Connors, Joseph M / Brooks-Wilson, Angela R

    Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology

    2020  Volume 29, Issue 6, Page(s) 1168–1178

    Abstract: Background: Familial aggregation of lymphoid cancers and immune-related disorders suggests a role for genetic susceptibility; however, few studies examine environmental factors. According to the hygiene hypothesis, adult-onset immune-related diseases ... ...

    Abstract Background: Familial aggregation of lymphoid cancers and immune-related disorders suggests a role for genetic susceptibility; however, few studies examine environmental factors. According to the hygiene hypothesis, adult-onset immune-related diseases may be a consequence of reduced childhood infectious exposures and aberrant immune development. In a cohort of 196 multiple-case lymphoid cancer families, we analyzed environmental factors related to the hygiene hypothesis.
    Methods: Family structure, childhood environment, and immune-related disorders were examined among 196 lymphoid cancer families, in relation to risk of lymphoid cancer. We report on 450 lymphoid cancer cases and 1,018 unaffected siblings using logistic regression models with generalized estimating equations to estimate ORs and 95% confidence intervals (CI) for association.
    Results: The risk of lymphoma tended to decrease with later birth order (OR = 0.83; 95% CI, 0.78-0.89) and larger sibship size (OR = 0.82; 95% CI, 0.79-0.85). High maternal education, above average family income during childhood, allergies (OR = 2.25; 95% CI, 1.44-3.51), and tonsillectomy (OR = 1.78; 95% CI, 1.14-2.78) were independent risk factors for lymphoma. Familial lymphoid cancer cases were more likely to report environment (OR = 1.90; 95% CI, 1.21-2.98) and drug (OR = 2.30; 95% CI, 1.41-3.73) allergies.
    Conclusions: These associations underscore the complex etiology of familial lymphoma. To our knowledge, this is the largest multiple-case family-based study that supports the hygiene hypothesis contributing to lymphoid cancer risk.
    Impact: Understanding the mechanism by which environmental and lifestyle factors affect lymphoid cancer risk may advance cancer prevention, even in the familial context.
    MeSH term(s) Birth Order ; Cancer Survivors/statistics & numerical data ; Female ; Humans ; Lymphoma/epidemiology ; Lymphoma/immunology ; Male ; Middle Aged ; Risk Factors
    Language English
    Publishing date 2020-03-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1153420-5
    ISSN 1538-7755 ; 1055-9965
    ISSN (online) 1538-7755
    ISSN 1055-9965
    DOI 10.1158/1055-9965.EPI-19-1204
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: In search of genetic factors predisposing to familial hairy cell leukemia (HCL): exome-sequencing of four multiplex HCL pedigrees.

    Pemov, Alexander / Pathak, Anand / Jones, Samantha J / Dewan, Ramita / Merberg, Jessica / Karra, Sirisha / Kim, Jung / Arons, Evgeny / Ravichandran, Sarangan / Luke, Brian T / Suman, Shalabh / Yeager, Meredith / Dyer, Martin J S / Lynch, Henry T / Greene, Mark H / Caporaso, Neil E / Kreitman, Robert J / Goldin, Lynn R / Spinelli, John J /
    Brooks-Wilson, Angela / McMaster, Mary L / Stewart, Douglas R

    Leukemia

    2020  Volume 34, Issue 7, Page(s) 1934–1938

    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Biomarkers, Tumor/genetics ; Female ; Follow-Up Studies ; Genetic Predisposition to Disease ; Germ-Line Mutation ; Humans ; Leukemia, Hairy Cell/genetics ; Leukemia, Hairy Cell/pathology ; Male ; Middle Aged ; Pedigree ; Prognosis ; Whole Exome Sequencing/methods
    Chemical Substances Biomarkers, Tumor
    Language English
    Publishing date 2020-01-28
    Publishing country England
    Document type Letter ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 807030-1
    ISSN 1476-5551 ; 0887-6924
    ISSN (online) 1476-5551
    ISSN 0887-6924
    DOI 10.1038/s41375-019-0702-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Nonrandom occurrence of lymphoid cancer types in 140 families.

    Jones, Samantha J / Voong, Jackson / Thomas, Ruth / English, Amy / Schuetz, Johanna / Slack, Graham W / Graham, Jinko / Connors, Joseph M / Brooks-Wilson, Angela

    Leukemia & lymphoma

    2017  Volume 58, Issue 9, Page(s) 1–10

    Abstract: We studied 140 families with two or more lymphoid cancers, including non-Hodgkin lymphoma (NHL), Hodgkin lymphoma (HL), chronic lymphocytic leukemia (CLL), and multiple myeloma (MM), for deviation from the population age of onset and lymphoid cancer co- ... ...

    Abstract We studied 140 families with two or more lymphoid cancers, including non-Hodgkin lymphoma (NHL), Hodgkin lymphoma (HL), chronic lymphocytic leukemia (CLL), and multiple myeloma (MM), for deviation from the population age of onset and lymphoid cancer co-occurrence patterns. Median familial NHL, HL, CLL and MM ages of onset are substantially earlier than comparable population data. NHL, HL and CLL (but not MM) also show earlier age of onset in later generations, known as anticipation. The co-occurrence of lymphoid cancers is significantly different from that expected based on population frequencies (p < .0001), and the pattern differs more in families with more affected members (p < .0001), suggesting specific lymphoid cancer combinations have a shared genetic basis. These families provide evidence for inherited factors that increase the risk of multiple lymphoid cancers. This study was approved by the BC Cancer Agency - University of British Columbia Clinical Research Ethics Board.
    MeSH term(s) Age of Onset ; Anticipation, Genetic ; Disease Susceptibility ; Family ; Female ; Genetic Predisposition to Disease ; Humans ; Leukemia, Lymphoid/epidemiology ; Leukemia, Lymphoid/etiology ; Lymphoma/epidemiology ; Lymphoma/etiology ; Male ; Pedigree ; SEER Program
    Language English
    Publishing date 2017-02-21
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1042374-6
    ISSN 1029-2403 ; 1042-8194
    ISSN (online) 1029-2403
    ISSN 1042-8194
    DOI 10.1080/10428194.2017.1281412
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: The Genome of the Northern Sea Otter (Enhydra lutris kenyoni).

    Jones, Samantha J / Haulena, Martin / Taylor, Gregory A / Chan, Simon / Bilobram, Steven / Warren, René L / Hammond, S Austin / Mungall, Karen L / Choo, Caleb / Kirk, Heather / Pandoh, Pawan / Ally, Adrian / Dhalla, Noreen / Tam, Angela K Y / Troussard, Armelle / Paulino, Daniel / Coope, Robin J N / Mungall, Andrew J / Moore, Richard /
    Zhao, Yongjun / Birol, Inanc / Ma, Yussanne / Marra, Marco / Jones, Steven J M

    Genes

    2017  Volume 8, Issue 12

    Abstract: The northern sea otter inhabits coastal waters of the northern Pacific Ocean and is the largest member of the Mustelidae family. DNA sequencing methods that utilize microfluidic partitioned and non-partitioned library construction were used to establish ... ...

    Abstract The northern sea otter inhabits coastal waters of the northern Pacific Ocean and is the largest member of the Mustelidae family. DNA sequencing methods that utilize microfluidic partitioned and non-partitioned library construction were used to establish the sea otter genome. The final assembly provided 2.426 Gbp of highly contiguous assembled genomic sequences with a scaffold N50 length of over 38 Mbp. We generated transcriptome data derived from a lymphoma to aid in the determination of functional elements. The assembled genome sequence and underlying sequence data are available at the National Center for Biotechnology Information (NCBI) under the BioProject accession number PRJNA388419.
    Language English
    Publishing date 2017-12-11
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527218-4
    ISSN 2073-4425
    ISSN 2073-4425
    DOI 10.3390/genes8120379
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: The Genome of the Beluga Whale (Delphinapterus leucas).

    Jones, Steven J M / Taylor, Gregory A / Chan, Simon / Warren, René L / Hammond, S Austin / Bilobram, Steven / Mordecai, Gideon / Suttle, Curtis A / Miller, Kristina M / Schulze, Angela / Chan, Amy M / Jones, Samantha J / Tse, Kane / Li, Irene / Cheung, Dorothy / Mungall, Karen L / Choo, Caleb / Ally, Adrian / Dhalla, Noreen /
    Tam, Angela K Y / Troussard, Armelle / Kirk, Heather / Pandoh, Pawan / Paulino, Daniel / Coope, Robin J N / Mungall, Andrew J / Moore, Richard / Zhao, Yongjun / Birol, Inanc / Ma, Yussanne / Marra, Marco / Haulena, Martin

    Genes

    2017  Volume 8, Issue 12

    Abstract: The beluga whale is a cetacean that inhabits arctic and subarctic regions, and is the only living member of the ... ...

    Abstract The beluga whale is a cetacean that inhabits arctic and subarctic regions, and is the only living member of the genus
    Language English
    Publishing date 2017-12-11
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527218-4
    ISSN 2073-4425
    ISSN 2073-4425
    DOI 10.3390/genes8120378
    Database MEDical Literature Analysis and Retrieval System OnLINE

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