Prolonged blooming season of flower plantings increases wild bee abundance and richness in agricultural landscapes
Neumüller, Ulrich, Burger, Hannah, Schwenninger, Hans Richard, Hopfenmüller, Sebastian, Krausch, Sabrina, Weiß, Karin, Ayasse, Manfred
Published in Biodiversity and conservation (01.09.2021)
Published in Biodiversity and conservation (01.09.2021)
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Journal Article
Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panels
Einhorn, Yaron, Einhorn, Moshe, Kurolap, Alina, Steinberg, Dror, Mory, Adi, Bazak, Lily, Paperna, Tamar, Grinshpun-Cohen, Julia, Basel-Salmon, Lina, Weiss, Karin, Singer, Amihood, Yaron, Yuval, Baris Feldman, Hagit
Published in Human genomics (28.03.2023)
Published in Human genomics (28.03.2023)
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Journal Article
SETD5 Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome
Crippa, Milena, Bestetti, Ilaria, Maitz, Silvia, Weiss, Karin, Spano, Alice, Masciadri, Maura, Smithson, Sarah, Larizza, Lidia, Low, Karen, Cohen, Lior, Finelli, Palma
Published in Frontiers in neurology (24.07.2020)
Published in Frontiers in neurology (24.07.2020)
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Journal Article
A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case Report
Pollack, Shirley, Eisenstein, Israel, Mory, Adi, Paperna, Tamar, Ofir, Ayala, Baris-Feldman, Hagit, Weiss, Karin, Veszeli, Nóra, Csuka, Dorottya, Shemer, Revital, Glaser, Fabian, Prohászka, Zoltán, Magen, Daniella
Published in Frontiers in immunology (24.06.2021)
Published in Frontiers in immunology (24.06.2021)
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Journal Article
RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric function
Samra, Nadra, Toubiana, Shir, Yttervik, Hilde, Tzur-Gilat, Aya, Morani, Ilham, Itzkovich, Chen, Giladi, Liran, Abu Jabal, Kamal, Cao, John Z, Godley, Lucy A, Mory, Adi, Baris Feldman, Hagit, Tveten, Kristian, Selig, Sara, Weiss, Karin
Published in Journal of human genetics (01.11.2021)
Published in Journal of human genetics (01.11.2021)
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Journal Article
SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly
Stokes, Bethany, Berger, Seth I., Hall, Beth A., Weiss, Karin, Martinez, Ariel F., Hadley, Donald W., Murdock, David R., Ramanathan, Subhadra, Clark, Robin D., Roessler, Erich, Kruszka, Paul, Muenke, Maximilian
Published in Congenital anomalies (01.01.2018)
Published in Congenital anomalies (01.01.2018)
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Journal Article
Publicly funded exome sequencing for outpatients with neurodevelopmental disorders demonstrates a high rate of unexpected findings impacting medical management
Nakhleh Francis, Yara, Hershkovitz, Tova, Ekhilevitch, Nina, Habib, Clair, Ravid, Sarit, Tal, Galit, Schertz, Mitchell, Mory, Adi, Zinger, Amihood, Baris Feldman, Hagit, Zaid, Rinat, Paperna, Tamar, Weiss, Karin
Published in Genetics in Medicine Open (2023)
Published in Genetics in Medicine Open (2023)
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Journal Article
Rare Disease Diagnostics: A Single-center Experience and Lessons Learnt
Weiss, Karin, Kurolap, Alina, Paperna, Tamar, Mory, Adi, Steinberg, Maya, Hershkovitz, Tova, Ekhilevitch, Nina, Baris, Hagit N
Published in Rambam Maimonides medical journal (30.07.2018)
Published in Rambam Maimonides medical journal (30.07.2018)
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Journal Article
Hybrid Solar-Geothermal Energy Absorption Air-Conditioning System Operating with NaOH-H2O—Las Tres Vírgenes (Baja California Sur), “La Reforma” Case
Galindo-Luna, Yuridiana, Gómez-Arias, Efraín, Romero, Rosenberg, Venegas-Reyes, Eduardo, Montiel-González, Moisés, Unland-Weiss, Helene, Pacheco-Hernández, Pedro, González-Fernández, Antonio, Díaz-Salgado, Jorge
Published in Energies (Basel) (01.05.2018)
Published in Energies (Basel) (01.05.2018)
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Journal Article
Aprendizagem organizacional: a experiência vivida por bibliotecários de uma biblioteca universitária
Faqueti, Marouva Fallgatter, Dutra, Sigrid Karin Weiss, Alves, João Bosco da Mota, Cunha, Cristiano José Castro de Almeida
Published in Biblios : revista electrónica de bibliotecología y ciencias de la información (07.12.2017)
Published in Biblios : revista electrónica de bibliotecología y ciencias de la información (07.12.2017)
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Journal Article
The clinical management of type 2 Gaucher disease
Weiss, Karin, Gonzalez, Ashley N., Lopez, Grisel, Pedoeim, Leah, Groden, Catherine, Sidransky, Ellen
Published in Molecular genetics and metabolism (01.02.2015)
Published in Molecular genetics and metabolism (01.02.2015)
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Journal Article
Favourite plants of wild bees
Kuppler, Jonas, Neumüller, Ulrich, Mayr, Antonia Veronika, Hopfenmüller, Sebastian, Weiss, Karin, Prosi, Rainer, Schanowski, Arno, Schwenninger, Hans-Richard, Ayasse, Manfred, Burger, Hannah
Published in Agriculture, ecosystems & environment (01.02.2023)
Published in Agriculture, ecosystems & environment (01.02.2023)
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Journal Article
eP174 - Exome sequencing for neurodevelopmental disorders and the effect on patient management – a single center experience
Weiss, Karin, Hershkovitz, Tova, Ekhilevitch, Nina, Zaid, Rinat, Mory, Adi, Feldman, Hagit Baris, Paperna, Tamar
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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Journal Article
Exome sequencing for neurodevelopmental disorders and the effect on patient management – a single center experience
Weiss, Karin, Hershkovitz, Tova, Ekhilevitch, Nina, Zaid, Rinat, Mory, Adi, Feldman, Hagit Baris, Paperna, Tamar
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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Journal Article
Rapid exome sequencing for children with severe acute encephalopathy – A case series
Habib, Clair, Paperna, Tamar, Zaid, Rinat, Ravid, Sarit, Ben Ari, Josef, Tal, Galit, Weiss, Karin, Hershkovitz, Tova
Published in European journal of medical genetics (01.04.2024)
Published in European journal of medical genetics (01.04.2024)
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Journal Article
A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with Holoprosencephaly
Kruszka, Paul, Berger, Seth I., Weiss, Karin, Everson, Joshua L., Martinez, Ariel F., Hong, Sungkook, Anyane-Yeboa, Kwame, Lipinski, Robert J., Muenke, Maximilian
Published in American journal of human genetics (02.05.2019)
Published in American journal of human genetics (02.05.2019)
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Journal Article
Holoprosencephaly from conception to adulthood
Weiss, Karin, Kruszka, Paul S., Levey, Eric, Muenke, Max
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.06.2018)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.06.2018)
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Journal Article
Refugees in Europe: national overviews from key countries with a special focus on child and adolescent mental health
Hodes, Matthew, Vasquez, Melisa Mendoza, Anagnostopoulos, Dimitris, Triantafyllou, Kalliopi, Abdelhady, Dalia, Weiss, Karin, Koposov, Roman, Cuhadaroglu, Fusun, Hebebrand, Johannes, Skokauskas, Norbert
Published in European child & adolescent psychiatry (01.04.2018)
Published in European child & adolescent psychiatry (01.04.2018)
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Journal Article
A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia
Cohen-Barak, Eran, Danial-Farran, Nada, Chervinsky, Elana, Alimi-Kasem, Ola, Zagairy, Fadia, Livneh, Ido, Mawassi, Bannan, Hreish, Maysa, Khayat, Morad, Lossos, Alexander, Meiner, Vardiella, Ehilevitch, Nina, Weiss, Karin, Shalev, Stavit
Published in Journal of medical genetics (01.03.2023)
Published in Journal of medical genetics (01.03.2023)
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Journal Article