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Introduction Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@11758f2a Item: Title: 2. Methods Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@e720b71 Children: Item: Title: 2.1. Recruitment of cases and high risk individuals Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@1b26f7b2 Item: Title: 2.2. Next generation sequencing of PDAC cases, high risk individuals and non-PDAC cases Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@491cc5c9 Item: Title: 2.3. Identification of potentially pathogenic mutations Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@74ad1f1f Item: Title: 2.4. Validation of pathogenic and likely pathogenic variants Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@6a1aab78 Item: Title: 2.5. Statistical analysis Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@462d5aee Item: Title: 3. Results Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@69b0fd6f Children: Item: Title: 3.1. Validation of the sequencing panel Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@757942a1 Item: Title: 3.2. Identification of pathogenic, likely pathogenic variants and potentially pathogenic VUS in PDAC cases Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@4a87761d Item: Title: 3.3. Potentially pathogenic VUS in cases with other cancer types and high risk individuals Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@66d1af89 Item: Title: 4. Discussion Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@8646db9 Item: Title: 5. Conclusion Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@37374a5e Item: Title: Declaration of Competing Interest Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@4671e53b Item: Title: Acknowledgments Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@2db7a79b Item: Title: Supplementary materials Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@6950e31 Children: Item: Title: References Destination: edu.harvard.hul.ois.jhove.module.pdf.PdfSimpleObject@b7dd107 Info: Title: A comprehensive analysis of candidate genes in familial pancreatic cancer families reveals a high frequency of potentially pathogenic germline variants Author: Julie Earl Subject: EBioMedicine, 53 (2020) 102675. doi:10.1016/j.ebiom.2020.102675 Keywords: Familial pancreatic cancer; Panel sequencing; DNA repair and hereditary cancer genes; Pathogenic variants Creator: Elsevier Producer: Acrobat Distiller 10.1.10 (Windows) CreationDate: Fri Mar 20 13:08:59 CET 2020 ModDate: Fri Mar 20 13:09:17 CET 2020 ID: 0xf8416262c244db03870af9635a795496, 0xd475fd868b90a488547442fe4e690c98 Filters: FilterPipeline: FlateDecode FilterPipeline: DCTDecode Images: Image: NisoImageMetadata: FormatName: image/jpg CompressionScheme: JPEG ImageWidth: 222 ImageHeight: 299 ColorSpace: RGB BitsPerSample: 8 BitsPerSampleUnit: integer Fonts: Type1: Font: BaseFont: FDEFKC+AdvP4C4E74 FontSubset: true FirstChar: 1 LastChar: 3 FontDescriptor: FontName: FDEFKC+AdvP4C4E74 Flags: Symbolic FontBBox: -20, -958, 1114, 770 FontFile3: true EncodingDictionary: Differences: true Font: BaseFont: FDEFDB+AdvOT5fa4e291 FontSubset: true FirstChar: 37 LastChar: 248 FontDescriptor: FontName: FDEFDB+AdvOT5fa4e291 Flags: Serif, Nonsymbolic FontBBox: -72, -250, 1041, 979 FontFile3: true Encoding: WinAnsiEncoding Font: BaseFont: FDEMPF+AdvTTb83ee1dd.B FontSubset: true FirstChar: 46 LastChar: 121 FontDescriptor: FontName: FDEMPF+AdvTTb83ee1dd.B Flags: Nonsymbolic FontBBox: -93, -250, 1041, 989 FontFile3: true Encoding: WinAnsiEncoding Font: BaseFont: FDEFJB+AdvOTf2586c63 FontSubset: true FirstChar: 40 LastChar: 122 FontDescriptor: FontName: FDEFJB+AdvOTf2586c63 Flags: Serif, Nonsymbolic FontBBox: -135, -229, 1052, 968 FontFile3: true Encoding: WinAnsiEncoding Font: BaseFont: FDEMPG+AdvP4C9543 FontSubset: true FirstChar: 1 LastChar: 163 FontDescriptor: FontName: FDEMPG+AdvP4C9543 Flags: Symbolic FontBBox: 0, -947, 1041, 895 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: FDEMGI+AdvPAC3D FontSubset: true FirstChar: 46 LastChar: 119 FontDescriptor: FontName: FDEMGI+AdvPAC3D Flags: Nonsymbolic FontBBox: -166, -239, 989, 791 FontFile3: true Encoding: WinAnsiEncoding Font: BaseFont: FDEFJA+AdvP4C4E59 FontSubset: true FirstChar: 2 LastChar: 160 FontDescriptor: FontName: FDEFJA+AdvP4C4E59 Flags: Symbolic FontBBox: -31, -250, 1000, 750 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: FDENIG+AdvOT1be73566.B FontSubset: true FirstChar: 49 LastChar: 89 FontDescriptor: FontName: FDENIG+AdvOT1be73566.B Flags: Nonsymbolic FontBBox: -166, -239, 1114, 989 FontFile3: true Encoding: WinAnsiEncoding Font: BaseFont: FDENCH+AdvP4C9542 FontSubset: true FirstChar: 60 LastChar: 62 FontDescriptor: FontName: FDENCH+AdvP4C9542 Flags: Nonsymbolic FontBBox: 0, -208, 979, 677 FontFile3: true Encoding: WinAnsiEncoding Font: BaseFont: FDEOMO+AdvP4A5FDB FontSubset: true FirstChar: 117 LastChar: 117 FontDescriptor: FontName: FDEOMO+AdvP4A5FDB Flags: Nonsymbolic FontBBox: 0, -239, 979, 718 FontFile3: true Encoding: WinAnsiEncoding Font: BaseFont: FDEFKD+AdvOT5fa4e291+20 FontSubset: true FirstChar: 145 LastChar: 150 FontDescriptor: FontName: FDEFKD+AdvOT5fa4e291+20 Flags: Nonsymbolic FontBBox: 19, -208, 947, 781 FontFile3: true Encoding: WinAnsiEncoding Font: BaseFont: FDEFKB+AdvOT5fa4e291+fb FontSubset: true FirstChar: 1 LastChar: 3 FontDescriptor: FontName: FDEFKB+AdvOT5fa4e291+fb Flags: Symbolic FontBBox: 40, 0, 572, 781 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true Font: BaseFont: FDENAH+AdvOTf2586c63+fb FontSubset: true FirstChar: 1 LastChar: 1 FontDescriptor: FontName: FDENAH+AdvOTf2586c63+fb Flags: Symbolic FontBBox: -114, -208, 833, 781 FontFile3: true EncodingDictionary: Differences: true ToUnicode: true XMP: 2020-03-20T17:08:59+05:30 Elsevier 2020-03-20T17:09:17+05:30 2020-03-20T17:09:17+05:30 Acrobat Distiller 10.1.10 (Windows) Familial pancreatic cancer,Panel sequencing,DNA repair and hereditary cancer genes,Pathogenic variants application/pdf doi:10.1016/j.ebiom.2020.102675 Elsevier B.V. EBioMedicine, 53 (2020) 102675. doi:10.1016/j.ebiom.2020.102675 Familial pancreatic cancer Panel sequencing DNA repair and hereditary cancer genes Pathogenic variants A comprehensive analysis of candidate genes in familial pancreatic cancer families reveals a high frequency of potentially pathogenic germline variants Julie Earl Cristina Galindo-Pumariño Jessica Encinas Emma Barreto Maria E. Castillo Vanessa Pachón Reyes Ferreiro Mercedes Rodríguez-Garrote Silvia González-Martínez Teresa Ramon y Cajal Luis Robles Diaz Isabel Chirivella-Gonzalez Montse Rodriguez Eva Martínez de Castro David García-Seisdedos Gloria Muñoz Juan Manuel Rosa Rosa Mirari Marquez Nuría Malats Alfredo Carrato uuid:fd8cfc10-4791-4a8b-8025-00abb91efa0c uuid:c243bbef-2d62-4cfc-a403-6c184dbac298 journal © 2020 The Author(s). Published by Elsevier B.V. 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