Medverkande i utredning : Jenny Welander

Berglund, Björn, Bich Hoang, Ngoc Thi, Tärnberg, Maria, Kien Le, Ngai, Nilsson, Maud, Khanh Khu, Dung Thi, Svartstrom, Olov, Welander, Jenny, Nilsson, Lennart E, Olson, Linus, Minh Dien, Tran, Thanh Le, Hai, Larsson, Mattias och Hanberger, Håkan, Molecular and phenotypic characterization of clinical isolates belonging to a KPC-2-producing strain of ST15 Klebsiella pneumoniae from a Vietnamese pediatric hospital [Elektronisk resurs], Antimicrobial Resistance and Infection Control, 2019, 8 nr 1

Toledo, Rodrigo A., Burnichon, Nelly, Cascon, Alberto, Benn, Diana E., Bayley, Jean-Pierre, Welander, Jenny, Tops, Carli M., Firth, Helen, Dwight, Trish, Ercolino, Tonino, Mannelli, Massimo, Opocher, Giuseppe, Clifton-Bligh, Roderick, Gimm, Oliver, Maher, Eamonn R., Robledo, Mercedes, Gimenez-Roqueplo, Anne-Paule och Dahia, Patricia L. M., Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas [Elektronisk resurs], Nature Reviews Endocrinology, 2017, 13 nr 4, 233–247

Stenman, Adam, Welander, Jenny, Gustavsson, Ida, Brunaud, Laurent, Backdahl, Martin, Söderkvist, Peter, Gimm, Oliver, Christofer Juhlin, C. och Larsson, Catharina, HRAS mutation prevalence and associated expression patterns in pheochromocytoma [Elektronisk resurs], Genes, Chromosomes and Cancer, 2016, 55 nr 5, 452–459

Christofer Juhlin, C., Stenman, Adam, Haglund, Felix, Clark, Victoria E., Brown, Taylor C., Baranoski, Jacob, Bilguvar, Kaya, Goh, Gerald, Welander, Jenny, Svahn, Fredrika, Rubinstein, Jill C., Caramuta, Stefano, Yasuno, Katsuhito, Guenel, Murat, Backdahl, Martin, Gimm, Oliver, Söderkvist, Peter, Prasad, Manju L., Korah, Reju, Lifton, Richard P. och Carling, Tobias, Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene [Elektronisk resurs], Genes, Chromosomes and Cancer, 2015, 54 nr 9, 542–554

Welander, Jenny, Genetic Alterations in Pheochromocytoma and Paraganglioma, 2015, Department of Clinical and Experimental Medicine, Linköping University, Linköping

Welander, Jenny, Genetic Alterations in Pheochromocytoma and Paraganglioma [Elektronisk resurs], 2015, Department of Clinical and Experimental Medicine, Linköping University, Linköping

Dutta, Ravi Kumar, Welander, Jenny, Brauckhoff, Michael, Walz, Martin, Alesina, Piero, Arnesen, Thomas, Söderkvist, Peter och Gimm, Oliver, Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas [Elektronisk resurs], Endocrine-Related Cancer, 2014, 21 nr 1, L1-L4

Kugelberg, Johan, Welander, Jenny, Schiavi, Francesca, Fassina, Ambrogio, Backdahl, Martin, Larsson, Catharina, Opocher, Giuseppe, Söderkvist, Peter, Dahia, Patricia L., Neumann, Hartmut P. H. och Gimm, Oliver, Role of SDHAF2 and SDHD in von Hippel-Lindau Associated Pheochromocytomas [Elektronisk resurs], World Journal of Surgery, 2014, 38 nr 3, 724–732

Tillmar, Andreas O, Dell'amico, Barbara, Welander, Jenny och Holmlund, Gunilla, A universal method for species identification of mammals utilizing next generation sequencing for the analysis of DNA mixtures [Elektronisk resurs], PLoS ONE, 2013, 8 nr 12, e83761

Berg, Emma och Welander, Jenny, Fri rörlighet och social trygghet förordningen (EEG) nr 1408/71 och den svenska socialförsäkringen i tillämpning, 2011, TPB, Johanneshov

Berg, Emma och Welander, Jenny, Fri rörlighet och social trygghet : förordningen (EEG) nr 1408/71 och den svenska socialförsäkringen i tillämpning, 2003, Juristförlaget : Akademibokhandeln i Lund [distributör] och Wallin & Dalholm boktryckeri, Lund och Lund

Welander, Jenny, Skolbibliotek : föredrag vid 10:e nordiska skolmötet i Stockholm 1910, Verdandi : tidskrift för ungdomens målsmän och vänner i hem och skola, 1910, 1910(28) nr 5–6, s. 257–264

Chamoun, Sherley, Welander, Jenny, Martis, Mihaela-Maria, Ntzouni, Maria, Claesson, Carina, Vikström, Elena och Turkina, Maria, Colistin Dependence in Extensively Drug-Resistant Acinetobacter baumannii Strain Is Associated with ISAjo2 and ISAba13 Insertions and Multiple Cellular Responses, International Journal of Molecular Sciences, 2021, 22 nr 2, : MDPI

Berglund, Björn, Bich Hoang, Ngoc Thi, Tärnberg, Maria, Kien Le, Ngai, Nilsson, Maud, Khanh Khu, Dung Thi, Svartström, Olov, Welander, Jenny, Nilsson, Lennart E, Olson, Linus, Minh Dien, Tran, Thanh Le, Hai, Larsson, Mattias, Hanberger, Håkan, Le, HT, Le, NK, Tarnberg, M, Dien, TM, Berglund, B, Hoang, NTB, Larsson, M, Khu, DTK, Nilsson, LE, Nilsson, M, Welander, J, Olson, L, Svartstrom, O och Hanberger, H, Molecular and phenotypic characterization of clinical isolates belonging to a KPC-2-producing strain of ST15 Klebsiella pneumoniae from a Vietnamese pediatric hospital, Antimicrobial Resistance and Infection Control, 2019, 8 nr 1, : BMC

Berglund, Björn, Chen, Baoli, Tärnberg, Maria, Sun, Qiang, Xu, Liuchen, Welander, Jenny, Li, Yan, Bi, Zhenwang, Nilsson, Maud och Nilsson, Lennart E, Characterization of extended-spectrum -lactamase-producing Escherichia coli harboring mcr-1 and toxin genes from human fecal samples from China, FUTURE COMPUTING … the … International Conference on Future Computational Technologies and Applications, 2018, 13 nr 15, s. 1647–1656, : FUTURE MEDICINE LTD

Berglund, Björn, Hoang, Ngoc Thi Bich, Tärnberg, Maria, Le, Ngai Kien, Welander, Jenny, Nilsson, Maud, Khu, Dung Thi Khanh, Nilsson, Lennart E., Olson, Linus, Le, Hai Thanh, Larsson, Mattias och Hanberger, Håkan, Colistin- and carbapenem-resistant Klebsiella pneumoniae carrying mcr-1 and bla(OXA-48) isolated at a paediatric hospital in Vietnam, Journal of Antimicrobial Chemotherapy, 2018, 73 nr 4, s. 1100–1102, : OXFORD UNIV PRESS

Berglund, Björn, Bich Hoang, Ngoc Thi, Tärnberg, Maria, Kien Le, Ngai, Svartström, Olov, Khanh Khu, Dung Thi, Nilsson, Maud, Thanh Le, Hai, Welander, Jenny, Olson, Linus, Larsson, Mattias, Nilsson, Lennart E, Hanberger, Håkan, Le, HT, Le, NK, Tarnberg, M, Berglund, B, Hoang, NTB, Larsson, M, Khu, DTK, Olson, L, Nilsson, M, Welander, J, Nilsson, LE, Svartstrom, O och Hanberger, H, Insertion sequence transpositions and point mutations in mgrB causing colistin resistance in a clinical strain of carbapenem-resistant Klebsiella pneumoniae from Vietnam, International Journal of Antimicrobial Agents, 2018, 51 nr 5, s. 789–793, : ELSEVIER SCIENCE BV

Welander, Jenny, Lysiak, Malgorzata, Brauckhoff, Michael, Brunaud, Laurent, Söderkvist, Peter och Gimm, Oliver, Activating FGFR1 mutations in sporadic pheochromocytoma, World Journal of Surgery, 2018, 42 nr 2, s. 482–489, : Springer

Bausch, Birke, Schiavi, Francesca, Ni, Ying, Welander, Jenny, Patocs, Attila, Ngeow, Joanne, Wellner, Ulrich, Malinoc, Angelica, Taschin, Elisa, Barbon, Giovanni, Lanza, Virginia, Söderkvist, Peter, Stenman, Adam, Larsson, Catharina, Svahn, Fredrika, Chen, Jin-Lian, Marquard, Jessica, Fraenkel, Merav, Walter, Martin A., Peczkowska, Mariola, Prejbisz, Aleksander, Jarzab, Barbara, Hasse-Lazar, Kornelia, Petersenn, Stephan, Moeller, Lars C., Meyer, Almuth, Reisch, Nicole, Trupka, Arnold, Brase, Christoph, Galiano, Matthias, Preuss, Simon F., Kwok, Pingling, Lendvai, Nikoletta, Berisha, Gani, Makay, Ozer, Boedeker, Carsten C., Weryha, Georges, Racz, Karoly, Januszewicz, Andrzej, Walz, Martin K., Gimm, Oliver, Opocher, Giuseppe, Eng, Charis, Neumann, Hartmut P. H., Barbon, G, Preuss, SF, Neumann, HPH, Ngeow, J, Wellner, U, Jarzab, B, Berisha, G, Boedeker, CC, Lanza, V, Schiavi, F, Taschin, E, Trupka, A, Brase, C, Petersenn, S, Gimm, O, Eng, C, Welander, J, Hasse-Lazar, K, Walter, MA, Meyer, A, Stenman, A, Bausch, B, Kwok, P, Weryha, G, Prejbisz, A, Walz, MK, Opocher, G, Makay, O, Malinoc, A, Racz, K, Patocs, A, Fraenkel, M, Soderkvist, P, Peczkowska, M, Galiano, M, Januszewicz, A, Lendvai, N, Reisch, N, Moeller, LC och Ni, Y, Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention, JAMA Oncology, 2017, 3 nr 9, s. 1204–1212, : AMER MEDICAL ASSOC

Toledo, Rodrigo A., Burnichon, Nelly, Cascon, Alberto, Benn, Diana E., Bayley, Jean-Pierre, Welander, Jenny, Tops, Carli M., Firth, Helen, Dwight, Trish, Ercolino, Tonino, Mannelli, Massimo, Opocher, Giuseppe, Clifton-Bligh, Roderick, Gimm, Oliver, Maher, Eamonn R., Robledo, Mercedes, Gimenez-Roqueplo, Anne-Paule och Dahia, Patricia L. M., Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas, Nature Reviews Endocrinology, 2017, 13 nr 4, s. 233–247, : NATURE PUBLISHING GROUP

Paulsson, Johan O., Svahn, F., Welander, Jenny, Brunaud, L., Söderkvist, Peter, Gimm, Oliver, Stenman, A. och Juhlin, C. C., Editorial Material: Absence of the BRAF V600E mutation in pheochromocytoma in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, vol 39, issue 6, pp 715–716, Journal of Endocrinological Investigation, 2016, 39 nr 6, s. 715–716, : SPRINGER

Stenman, Adam, Welander, Jenny, Gustavsson, Ida, Brunaud, Laurent, Backdahl, Martin, Söderkvist, Peter, Gimm, Oliver, Christofer Juhlin, C., Larsson, Catharina, Soderkvist, P, Backdahl, M, Gustavsson, I, Larsson, C, Brunaud, L, Juhlin, CC, Welander, J, Gimm, O och Stenman, A, HRAS mutation prevalence and associated expression patterns in pheochromocytoma, Genes, Chromosomes and Cancer, 2016, 55 nr 5, s. 452–459, : WILEY-BLACKWELL

Christofer Juhlin, C., Stenman, Adam, Haglund, Felix, Clark, Victoria E., Brown, Taylor C., Baranoski, Jacob, Bilguvar, Kaya, Goh, Gerald, Welander, Jenny, Svahn, Fredrika, Rubinstein, Jill C., Caramuta, Stefano, Yasuno, Katsuhito, Guenel, Murat, Backdahl, Martin, Gimm, Oliver, Söderkvist, Peter, Prasad, Manju L., Korah, Reju, Lifton, Richard P., Carling, Tobias, Clark, VE, Carling, T, Lifton, RP, Gunel, M, Goh, G, Prasad, ML, Rubinstein, JC, Juhlin, CC, Svahn, F, Korah, R, Haglund, F, Bilguvar, K, Yasuno, K, Brown, TC, Soderkvist, P, Backdahl, M, Baranoski, J, Caramuta, S, Welander, J, Gimm, O och Stenman, A, Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene, Genes, Chromosomes and Cancer, 2015, 54 nr 9, s. 542–554, : Wiley: 12 months

Stenman, Adam, Svahn, Fredrika, Welander, Jenny, Gustavson, Boel, Söderkvist, Peter, Gimm, Oliver, Juhlin, C Christofer, Gustavson, B, Soderkvist, P, Welander, J, Svahn, F, Gimm, O, Juhlin, C och Stenman, A, Immunohistochemical NF1 Analysis Does not Predict NF1 Gene Mutation Status in Pheochromocytoma., Endocrine pathology, 2015, 26 nr 1, s. 9–14, : Springer

Welander, Jenny, Genetic Alterations in Pheochromocytoma and Paraganglioma, 2015, Linköping University Electronic Press, Linköping

Dutta, Ravi Kumar, Welander, Jenny, Brauckhoff, Michael, Walz, Martin, Alesina, Piero, Arnesen, Thomas, Söderkvist, Peter och Gimm, Oliver, Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas, Endocrine-Related Cancer, 2014, 21 nr 1, s. L1-L4, : Bioscientifica

Jerhammar, Fredrik, Johansson, Ann-Charlotte, Ceder, Rebecca, Welander, Jenny, Jansson, Agneta, Grafstrom, Roland C., Söderkvist, Peter, Roberg, Karin, Soderkvist, P, Johansson, AC, Jerhammar, F, Roberg, K, Welander, J, Grafstrom, RC, Ceder, R och Jansson, A, YAP1 is a potential biomarker for cetuximab resistance in head and neck cancer, Oral Oncology, 2014, 50 nr 9, s. 832–839, : Elsevier

Kugelberg, Johan, Welander, Jenny, Schiavi, Francesca, Fassina, Ambrogio, Backdahl, Martin, Larsson, Catharina, Opocher, Giuseppe, Söderkvist, Peter, Dahia, Patricia L., Neumann, Hartmut P. H., Gimm, Oliver, Soderkvist, P, Backdahl, M, Neumann, HPH, Dahia, PL, Larsson, C, Opocher, G, Welander, J, Fassina, A, Gimm, O, Schiavi, F och Kugelberg, J, Role of SDHAF2 and SDHD in von Hippel-Lindau Associated Pheochromocytomas, World Journal of Surgery, 2014, 38 nr 3, s. 724–732, : Springer Verlag (Germany)

Welander, Jenny, Andreasson, Adam, Brauckhoff, Michael, Backdahl, Martin, Larsson, Catharina, Gimm, Oliver och Söderkvist, Peter, Frequent EPAS1/HIF2 alpha exons 9 and 12 mutations in non-familial pheochromocytoma, Endocrine-Related Cancer, 2014, 21 nr 3, s. 495–504, : BioScientifica

Welander, Jenny, Andreasson, Adam, Juhlin, C. Christofer, Wiseman, Roger W., Backdahl, Martin, Hoog, Anders, Larsson, Catharina, Gimm, Oliver, Söderkvist, Peter, Soderkvist, P, Backdahl, M, Hoog, A, Wiseman, RW, Larsson, C, Juhlin, CC, Welander, J, Gimm, O och Andreasson, A, Rare Germline Mutations Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma, Journal of Clinical Endocrinology and Metabolism, 2014, 99 nr 7, s. E1352-E1360, : Endocrine Society

Tillmar, Andreas O, Dell'amico, Barbara, Welander, Jenny och Holmlund, Gunilla, A universal method for species identification of mammals utilizing next generation sequencing for the analysis of DNA mixtures, PLoS ONE, 2013, 8 nr 12, s. e83761-, : Public Library of Science

Welander, Jenny, Garvin, Stina, Bohnmark, Rickard, Isaksson, Lars, Wiseman, Roger W., Söderkvist, Peter och Gimm, Oliver, Editorial Material: Germline SDHA Mutation Detected by Next-Generation Sequencing in a Young Index Patient With Large Paraganglioma, Journal of Clinical Endocrinology and Metabolism, 2013, 98 nr 8, s. E1379-E1380, : Endocrine Society

Welander, Jenny, Söderkvist, Peter och Gimm, Oliver, The NF1 gene: a frequent mutational target in sporadic pheochromocytomas and beyond, Endocrine-Related Cancer, 2013, 20 nr 4, s. C13-C17, : BioScientifica

Kling, Daniel, Welander, Jenny, Tillmar, Andreas, Skare, Oivind, Egeland, Thore och Holmlund, Gunilla, DNA microarray as a tool in establishing genetic relatedness-Current status and future prospects, Forensic Science International, 2012, 6 nr 3, s. 322–329, : Elsevier

Welander, Jenny, Larsson, Catharina, Backdahl, Martin, Niyaz, Niyaz, Sivlér, Tobias, Brauckhoff, Michael, Söderkvist, Peter, Gimm, Oliver, Soderkvist, P, Backdahl, M, Brauckhoff, M, Larsson, C, Sivler, T, Welander, J, Hareni, N och Gimm, O, Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas, Human Molecular Genetics, 2012, 21 nr 26, s. 5406–5416, : Oxford University Press (OUP): Policy B

Jerhammar, Fredrik, Welander, Jenny, Johansson, A C, Söderkvist, Peter och Roberg, Karin, Gene Copy Number as Predictive Marker for Cetuximab Resistance in Head and Neck Squamous Cell Carcinomas in EUROPEAN JOURNAL OF CANCER, vol 47, issue, pp S571-S571, EUROPEAN JOURNAL OF CANCER, 2011,, s. S571-S571, : Elsevier

Welander, Jenny, Söderkvist, Peter och Gimm, Oliver, Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas, Endocrine-Related Cancer, 2011, 18 nr 6, s. 253–276