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Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives
Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives
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Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives

Kasak, Laura ; Laan, Maris

Human genetics, 2021-01, Vol.140 (1), p.135-154 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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Effects of RNA integrity on transcript quantification by total RNA sequencing of clinically collected human placental samples
Effects of RNA integrity on transcript quantification by total RNA sequencing of clinically collected human placental samples
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Effects of RNA integrity on transcript quantification by total RNA sequencing of clinically collected human placental samples

Reiman, Mario ; Laan, Maris ; Rull, Kristiina ; Sõber, Siim

The FASEB journal, 2017-08, Vol.31 (8), p.3298-3308 [Periódico revisado por pares]

United States: Federation of American Societies for Experimental Biology

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3
Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia
Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia
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Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia

Kasak, Laura ; Punab, Margus ; Nagirnaja, Liina ; Grigorova, Marina ; Minajeva, Ave ; Lopes, Alexandra M. ; Punab, Anna Maria ; Aston, Kenneth I. ; Carvalho, Filipa ; Laasik, Eve ; Smith, Lee B. ; Conrad, Donald F. ; Laan, Maris

American journal of human genetics, 2018-08, Vol.103 (2), p.200-212 [Periódico revisado por pares]

United States: Elsevier Inc

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4
The decline of FANCM immunohistochemical expression in prostate cancer stroma correlates with the grade group
The decline of FANCM immunohistochemical expression in prostate cancer stroma correlates with the grade group
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The decline of FANCM immunohistochemical expression in prostate cancer stroma correlates with the grade group

Dzaparidze, Georgi ; Anion, Evelin ; Laan, Maris ; Minajeva, Ave

Pathology international, 2020-08, Vol.70 (8), p.542-550 [Periódico revisado por pares]

Australia: Wiley Subscription Services, Inc

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5
A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans
A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans
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A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans

Hallast, Pille ; Kibena, Laura ; Punab, Margus ; Arciero, Elena ; Rootsi, Siiri ; Grigorova, Marina ; Flores, Rodrigo ; Jobling, Mark A ; Poolamets, Olev ; Pomm, Kristjan ; Korrovits, Paul ; Rull, Kristiina ; Xue, Yali ; Tyler-Smith, Chris ; Laan, Maris

eLife, 2021-03, Vol.10 [Periódico revisado por pares]

England: eLife Science Publications, Ltd

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6
Coordinated Expressional Landscape of the Human Placental miRNome and Transcriptome
Coordinated Expressional Landscape of the Human Placental miRNome and Transcriptome
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Coordinated Expressional Landscape of the Human Placental miRNome and Transcriptome

Inno, Rain ; Kikas, Triin ; Lillepea, Kristiina ; Laan, Maris

Frontiers in cell and developmental biology, 2021-07, Vol.9, p.697947-697947 [Periódico revisado por pares]

Frontiers Media S.A

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7
Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension
Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension
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Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension

Padmanabhan, Sandosh ; Melander, Olle ; Johnson, Toby ; Di Blasio, Anna Maria ; Lee, Wai K ; Gentilini, Davide ; Hastie, Claire E ; Menni, Cristina ; Monti, Maria Cristina ; Delles, Christian ; Laing, Stewart ; Corso, Barbara ; Navis, Gerjan ; Kwakernaak, Arjan J ; van der Harst, Pim ; Bochud, Murielle ; Maillard, Marc ; Burnier, Michel ; Hedner, Thomas ; Kjeldsen, Sverre ; Wahlstrand, Björn ; Sjögren, Marketa ; Fava, Cristiano ; Montagnana, Martina ; Danese, Elisa ; Torffvit, Ole ; Hedblad, Bo ; Snieder, Harold ; Connell, John M C ; Brown, Morris ; Samani, Nilesh J ; Farrall, Martin ; Cesana, Giancarlo ; Mancia, Giuseppe ; Signorini, Stefano ; Grassi, Guido ; Eyheramendy, Susana ; Wichmann, H Erich ; Laan, Maris ; Strachan, David P ; Sever, Peter ; Shields, Denis Colm ; Stanton, Alice ; Vollenweider, Peter ; Teumer, Alexander ; Völzke, Henry ; Rettig, Rainer ; Newton-Cheh, Christopher ; Arora, Pankaj ; Zhang, Feng ; Soranzo, Nicole ; Spector, Timothy D ; Lucas, Gavin ; Kathiresan, Sekar ; Siscovick, David S ; Luan, Jian'an ; Loos, Ruth J F ; Wareham, Nicholas J ; Penninx, Brenda W ; Nolte, Ilja M ; McBride, Martin ; Miller, William H ; Nicklin, Stuart A ; Baker, Andrew H ; Graham, Delyth ; McDonald, Robert A ; Pell, Jill P ; Sattar, Naveed ; Welsh, Paul ; Munroe, Patricia ; Caulfield, Mark J ; Zanchetti, Alberto ; Dominiczak, Anna F Schork, Nicholas J.

PLoS genetics, 2010-10, Vol.6 (10), p.e1001177-e1001177 [Periódico revisado por pares]

United States: Public Library of Science

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8
Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomes
Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomes
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Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomes

Sõber, Siim ; Reiman, Mario ; Kikas, Triin ; Rull, Kristiina ; Inno, Rain ; Vaas, Pille ; Teesalu, Pille ; Marti, Jesus M Lopez ; Mattila, Pirkko ; Laan, Maris

Scientific reports, 2015-08, Vol.5 (1), p.13336-13336, Article 13336 [Periódico revisado por pares]

England: Nature Publishing Group

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9
Diverse monogenic subforms of human spermatogenic failure
Diverse monogenic subforms of human spermatogenic failure
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Diverse monogenic subforms of human spermatogenic failure

Nagirnaja, Liina ; Lopes, Alexandra M ; Charng, Wu-Lin ; Miller, Brian ; Stakaitis, Rytis ; Golubickaite, Ieva ; Stendahl, Alexandra ; Luan, Tianpengcheng ; Friedrich, Corinna ; Mahyari, Eisa ; Fadial, Eloise ; Kasak, Laura ; Vigh-Conrad, Katinka ; Oud, Manon S ; Xavier, Miguel J ; Cheers, Samuel R ; James, Emma R ; Guo, Jingtao ; Jenkins, Timothy G ; Riera-Escamilla, Antoni ; Barros, Alberto ; Carvalho, Filipa ; Fernandes, Susana ; Gonçalves, João ; Gurnett, Christina A ; Jørgensen, Niels ; Jezek, Davor ; Jungheim, Emily S ; Kliesch, Sabine ; McLachlan, Robert I ; Omurtag, Kenan R ; Pilatz, Adrian ; Sandlow, Jay I ; Smith, James ; Eisenberg, Michael L ; Hotaling, James M ; Jarvi, Keith A ; Punab, Margus ; Rajpert-De Meyts, Ewa ; Carrell, Douglas T ; Krausz, Csilla ; Laan, Maris ; O'Bryan, Moira K ; Schlegel, Peter N ; Tüttelmann, Frank ; Veltman, Joris A ; Almstrup, Kristian ; Aston, Kenneth I ; Conrad, Donald F

Nature communications, 2022-12, Vol.13 (1), p.7953-7953, Article 7953 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia
Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia
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Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia

Salas-Huetos, Albert ; Tüttelmann, Frank ; Wyrwoll, Margot J. ; Kliesch, Sabine ; Lopes, Alexandra M. ; Goncalves, João ; Boyden, Steven E. ; Wöste, Marius ; Hotaling, James M. ; Nagirnaja, Liina ; Conrad, Donald F. ; Carrell, Douglas T. ; Aston, Kenneth I.

Human genetics, 2021-01, Vol.140 (1), p.217-227 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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