303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank von Henne, S.K., Aldisi, R., Sivalingam, S., Hochfeld, L.M., Maj, C., Borisov, O., Nöthen, M.M., Krawitz, P.M., Heilmann-Heimbach, S.

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Development Of Innovative Indoor/outdoor Air Quality Monitoring For Environmental Impact Assessment In The State Of Qatar von Alassi, A, Khan, A, Ayesh, D, Aljayyousi, I, Aldisi, R, Elasad, S, Touati, F, Benammar, M

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Re-curation and rational enrichment of knowledge graphs in Biological Expression Language von Hoyt, C.T, Domingo-Fernández, D, Aldisi, R, Xu, L, Kolpeja, K, Spalek, S, Wollert, E, Bachman, J, Gyori, B.M, Greene, P, Hofmann-Apitius, M

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Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence von Hassanin, Emadeldin, Spier, Isabel, Bobbili, Dheeraj R, Aldisi, Rana, Klinkhammer, Hannah, David, Friederike, Dueñas, Nuria, Hüneburg, Robert, Perne, Claudia, Brunet, Joan, Capella, Gabriel, Nöthen, Markus M, Forstner, Andreas J, Mayr, Andreas, Krawitz, Peter, May, Patrick, Aretz, Stefan, Maj, Carlo

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Performance evaluation of four type-specific commercial assays for detection of herpes simplex virus type 1 antibodies in a Middle East and North Africa population von Aldisi, Rana S., Elsidiq, Malaz S., Dargham, Soha R., Sahara, Afifah S., Al-Absi, Enas S., Nofal, Mariam Y., Mohammed, Layla I., Abu-Raddad, Laith J., Nasrallah, Gheyath K.

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Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence von Hassanin, Emadeldin, Spier, Isabel, Bobbili, Dheeraj R, Aldisi, Rana, Klinkhammer, Hannah, David, Friederike, Dueñas, Nuria, Hüneburg, Robert, Perne, Claudia, Brunet, Joan, Capella, Gabriel, Nöthen, Markus M, Forstner, Andreas J, Mayr, Andreas, Krawitz, Peter, May, Patrick, Aretz, Stefan, Maj, Carlo

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Additional file 1 of Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence von Hassanin, Emadeldin, Spier, Isabel, Bobbili, Dheeraj R., Aldisi, Rana, Klinkhammer, Hannah, David, Friederike, Dueñas, Nuria, Hüneburg, Robert, Perne, Claudia, Brunet, Joan, Capella, Gabriel, Nöthen, Markus M., Forstner, Andreas J., Mayr, Andreas, Krawitz, Peter, May, Patrick, Aretz, Stefan, Maj, Carlo

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Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence von Hassanin, Emadeldin, Spier, Isabel, Bobbili, Dheeraj R, Aldisi, Rana, Klinkhammer, Hannah, David, Friederike, Dueéas, Nuria, Hüneburg, Robert, Perne, Claudia, Brunet, Joan, Capella, Gabriel, Nöthen, Markus M, Forstner, Andreas J, Mayr, Andreas, Krawitz, Peter, May, Patrick, Aretz, Stefan, Maj, Carlo

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Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence von Hassanin, Emadeldin, Spier, Isabel, Bobbili, Dheeraj R, Aldisi, Rana, Klinkhammer, Hannah, David, Friederike, Dueéas, Nuria, Hüneburg, Robert, Perne, Claudia, Brunet, Joan, Capella, Gabriel, Nöthen, Markus M, Forstner, Andreas J, Mayr, Andreas, Krawitz, Peter, May, Patrick, Aretz, Stefan, Maj, Carlo

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