Jens Michael Hertz - Publications, H-index & Citations

Jens Michael Hertz

University of Southern Denmark

40H指数

196论文数

5.7K被引数

收录论文 45

发表时间

Impact of fluconazole in vasopressin 2 receptor-related congenital arginine vasopressin resistance 氟康唑对精氨酸加压素2受体相关先天性精氨酸加压素抵抗的影响

Kidney International

IF12.6

2026-09-24

PREAI

Line A. Mortensen; Claus Bistrup; Søren Rittig; Jens Michael Hertz; Kai M. Schmidt-Ott; Enno Klussman; Christian Hinze; Boye L. Jensen; Gitte R. Hinrichs

IVF patient subgroups benefit from preimplantation genetic testing for aneuploidy: a prospective multicentre cohort study IVF患者亚组从胚胎植入前非整倍体遗传学检测中受益：一项前瞻性多中心队列研究

Reproductive Biomedicine Online

IF3.5

2026-05-14

OAAI

Sofie Lykke Møller; Maria Borgstrøm; Johnny Hindkjær; Ulrik Schiøler Kesmodel; Jeanette Bogstad; Majbritt busk Madsen; Daniela Alosi; Morten Rønn Petersen; Jørn Aagaard; Aboubakar Cissé; Kristina Wendelboe Olsen; Laura Kristine Sønderberg Roos; Jens Michael Hertz; Kasper Madsen; Anna Klajnbard; Bugge Nøhr; Marie Louise Grøndahl

The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder KDM6B相关的神经发育障碍的临床与分子谱

The American Journal of Human Genetics

IF0

2025-10-18

PREAI

Dmitrijs Rots; Taryn E. Jakub; Crystal Keung; Adam Jackson; Siddharth Banka; Rolph Pfundt; Bert B.A. de Vries; Richard H. van Jaarsveld; Saskia M.J. Hopman; Ellen van Binsbergen; Irene Valenzuela; Maja Hempel; Tatjana Bierhals; Fanny Kortüm; Francois Lecoquierre; Alice Goldenberg; Jens Michael Hertz; Charlotte Brasch Andersen; Maria Kibæk; Eloise J. Prijoles; Roger E. Stevenson; David B. Everman; Wesley G. Patterson; Linyan Meng; Charul Gijavanekar; Karl De Dios; Shenela Lakhani; Tess Levy; Matias Wagner; Dagmar Wieczorek; Paul J. Benke; María Soledad Lopez Garcia; Renee Perrier; Sergio B. Sousa; Pedro M. Almeida; Maria José Simões; Bertrand Isidor; Wallid Deb; Andrew A. Schmanski; Omar Abdul-Rahman; Christophe Philippe; Ange-Line Bruel; Laurence Faivre; Antonio Vitobello; Christel Thauvin; Jeroen J. Smits; Livia Garavelli; Stefano G. Caraffi; Francesca Peluso; Laura Davis-Keppen; Dylan Platt; Erin Royer; Lisette Leeuwen; Margje Sinnema; Alexander P.A. Stegmann; Constance T.R.M. Stumpel; George E. Tiller; Daniëlle G.M. Bosch; Stephanus T. Potgieter; Shelagh Joss; Miranda Splitt; Simon Holden; Matina Prapa; Nicola Foulds; Sofia Douzgou; Kaija Puura; Regina Waltes; Andreas G. Chiocchetti; Christine M. Freitag; F. Kyle Satterstrom; Silvia De Rubeis; Joseph Buxbaum; Bruce D. Gelb; Aleksic Branko; Itaru Kushima; Jennifer Howe; Stephen W. Scherer; Alessia Arado; Chiara Baldo; Olivier Patat; Demeer Bénédicte; Diego Lopergolo; Filippo M. Santorelli; Tobias B. Haack; Andreas Dufke; Miriam Bertrand; Ruth J. Falb; Angelika Rieß; Peter Krieg; Stephanie Spranger; Maria Francesca Bedeschi; Maria Iascone; Sarah Josephi-Taylor; Tony Roscioli; Michael F. Buckley; Jan Liebelt; Aditi I. Dagli; Emmelien Aten; Anna C.E. Hurst; Alesha Hicks; Mohnish Suri; Ermal Aliu; Sunil Naik; Richard Sidlow; Juliette Coursimault; Gaël Nicolas; Hanna Küpper; Florence Petit; Veyan Ibrahim; Deniz Top; Francesca Di Cara; Raymond J. Louie; Elliot Stolerman; Han G. Brunner; Lisenka E.L.M. Vissers; Jamie M. Kramer; Tjitske Kleefstra

The effect of fluconazole on polyuria and urine concentration ability in nephrogenic diabetes insipidus 氟康唑对肾性尿崩症中多尿和尿液浓缩能力的影响

Nephrology Dialysis Transplantation

IF5.6

2025-10-01

PREAI

Mortensen, Line Aas; Bistrup, Claus; Jensen, Boye L.; Hertz, Jens Michael; Schmidt-Ott, Kai; Klussman, Enno; Hinze, Christian; Hinrichs, Gitte Rye

The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder KDM6B-related神经发育障碍的临床和分子谱

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2023-06-01

OAAI

Rots, Dmitrijs; Jakub, Taryn E.; Keung, Crystal; Lisenka, Vissers E. L. M.; Banka, Siddharth; Pfundt, Rolph; de Vries, Bert B. A.; van Jaarsveld, Richard H.; Hopman, Saskia M. J.; van Binsbergen, Ellen; Valenzuela, Irene; Hempel, Maja; Bierhals, Tatjana; Kortuem, Fanny; Lecoquierre, Francois; Goldenberg, Alice; Hertz, Jens Michael; Andersen, Charlotte Brasch; Kibaek, Maria; Prijoles, Eloise J.; Stevenson, Roger E.; Everman, David B.; Patterson, Wesley G.; Meng, Linyan; Gijavanekar, Charul; De Dios, Karl; Lakhani, Shenela; Levy, Tess; Wagner, Matias; Wieczorek, Dagmar; Benke, Paul J.; Garcia, Maria Soledad Lopez; Perrier, Renee; Sousa, Sergio B.; Almeida, Pedro M.; Simoes, Maria Jose; Isidor, Bertrand; Deb, Wallid; Schmanski, Andrew A.; Abdul-Rahman, Omar; Philippe, Christophe; Bruel, Ange-Line; Faivre, Laurence; Vitobello, Antonio; Thauvin, Christel; Smits, Jeroen J.; Garavelli, Livia; Caraffi, Stefano G.; Peluso, Francesca; Davis-Keppen, Laura; Platt, Dylan; Royer, Erin; Leeuwen, Lisette; Sinnema, Margje; Stegmann, Alexander P. A.; Stumpel, Constance T. R. M.; Tiller, George E.; Bosch, Danielle G. M.; Potgieter, Stephanus T.; Joss, Shelagh; Splitt, Miranda; Holden, Simon; Prapa, Matina; Foulds, Nicola; Douzgou, Sofia; Puura, Kaija; Waltes, Regina; Chiocchetti, Andreas G.; Freitag, Christine M.; Satterstrom, F. Kyle; De Rubeis, Silvia; Buxbaum, Joseph; Gelb, Bruce D.; Branko, Aleksic; Kushima, Itaru; Howe, Jennifer; Scherer, Stephen W.; Arado, Alessia; Baldo, Chiara; Patat, Olivier; Benedicte, Demeer; Lopergolo, Diego; Santorelli, Filippo M.; Haack, Tobias B.; Dufke, Andreas; Bertrand, Miriam; Falb, Ruth J.; Riess, Angelika; Krieg, Peter; Spranger, Stephanie; Bedeschi, Maria Francesca; Iascone, Maria; Josephi-Taylor, Sarah; Roscioli, Tony; Buckley, Michael F.; Liebelt, Jan; Dagli, Aditi I.; Aten, Emmelien; Hurst, Anna C. E.; Hicks, Alesha; Suri, Mohnish; Aliu, Ermal; Naik, Sunil; Sidlow, Richard; Coursimault, Juliette; Nicolas, Gael; Kuepper, Hanna; Petit, Florence; Ibrahim, Veyan; Top, Deniz; Di Cara, Francesca; Louie, Raymond J.; Stolerman, Elliot; Brunner, Han G.; Vissers, Lisenka E. L. M.; Kramer, Jamie M.; Kleefstra, Tjitske

Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria (vol 29, pg 1186, 2021)

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2023-01-31

OAAI

Savige, Judy; Storey, Helen; Watson, Elizabeth; Hertz, Jens Michael; Deltas, Constantinos; Renieri, Alessandra; Mari, Francesca; Hilbert, Pascale; Plevova, Pavlina; Byers, Peter; Cerkauskaite, Agne; Gregory, Martin; Cerkauskiene, Rimante; Ljubanovic, Danica Galesic; Becherucci, Francesca; Errichiello, Carmela; Massella, Laura; Aiello, Valeria; Lennon, Rachel; Hopkinson, Louise; Koziell, Ania; Lungu, Adrian; Rothe, Hansjorg Martin; Hoefele, Julia; Zacchia, Miriam; Martic, Tamara Nikuseva; Gupta, Asheeta; van Eerde, Albertien; Gear, Susie; Landini, Samuela; Palazzo, Viviana; al-Rabadi, Laith; Claes, Kathleen; Corveleyn, Anniek; Van Hoof, Evelien; van Geel, Micheel; Williams, Maggie; Ashton, Emma; Belge, Hendica; Ars, Elisabeth; Bierzynska, Agnieszka; Gangemi, Concetta; Lipska-Zietkiewicz, Beata S.

Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort 拥抱单基因帕金森病: MJFF全球遗传PD队列

MOVEMENT DISORDERS

IF7.6

2023-01-24

OAAI

Vollstedt, Eva-Juliane; Schaake, Susen; Lohmann, Katja; Padmanabhan, Shalini; Brice, Alexis; Lesage, Suzanne; Tesson, Christelle; Vidailhet, Marie; Wurster, Isabel; Hentati, Faycel; Mirelman, Anat; Giladi, Nir; Marder, Karen; Waters, Cheryl; Fahn, Stanley; Kasten, Meike; Bruggemann, Norbert; Borsche, Max; Foroud, Tatiana; Tolosa, Eduardo; Garrido, Alicia; Annesi, Grazia; Gagliardi, Monica; Bozi, Maria; Stefanis, Leonidas; Ferreira, Joaquim J.; Guedes, Leonor Correia; Avenali, Micol; Petrucci, Simona; Clark, Lorraine; Fedotova, Ekaterina Y.; Abramycheva, Natalya Y.; Alvarez, Victoria; Menendez-Gonzalez, Manuel; Maestre, Silvia Jesus; Gomez-Garre, Pilar; Mir, Pablo; Belin, Andrea Carmine; Ran, Caroline; Lin, Chin-Hsien; Kuo, Ming-Che; Crosiers, David; Wszolek, Zbigniew K.; Ross, Owen A.; Jankovic, Joseph; Nishioka, Kenya; Funayama, Manabu; Clarimon, Jordi; Williams-Gray, Caroline H.; Camacho, Marta; Cornejo-Olivas, Mario; Torres-Ramirez, Luis; Wu, Yih-Ru; Lee-Chen, Guey-Jen; Morgadinho, Ana; Pulkes, Teeratorn; Termsarasab, Pichet; Berg, Daniela; Kuhlenbaumer, Gregor; Kuhn, Andrea A.; Borngraeber, Friederike; de Michele, Giuseppe; De Rosa, Anna; Zimprich, Alexander; Puschmann, Andreas; Mellick, George D.; Dorszewska, Jolanta; Carr, Jonathan; Ferese, Rosangela; Gambardella, Stefano; Chase, Bruce; Markopoulou, Katerina; Satake, Wataru; Toda, Tatsushi; Rossi, Malco; Merello, Marcelo; Lynch, Timothy; Olszewska, Diana A.; Lim, Shen-Yang; Ahmad-Annuar, Azlina; Tan, Ai Huey; Al-Mubarak, Bashayer; Hanagasi, Hasmet; Koziorowski, Dariusz; Ertan, Sibel; Genc, Gencer; Aguiar, Patricia de Carvalho; Barkhuizen, Melinda; Pimentel, Marcia M. G.; Saunders-Pullman, Rachel; van de Warrenburg, Bart; Bressman, Susan; Toft, Mathias; Appel-Cresswell, Silke; Lang, Anthony E.; Skorvanek, Matej; Boon, Agnita J. W.; Kruger, Rejko; Sammler, Esther M.; Tumas, Vitor; Zhang, Bao-Rong; Garraux, Gaetan; Chung, Sun Ju; Kim, Yun Joong; Winkelmann, Juliane; Sue, Carolyn M.; Tan, Eng-King; Damasio, Joana; Klivenyi, Peter; Kostic, Vladimir S.; Arkadir, David; Martikainen, Mika; Borges, Vanderci; Hertz, Jens Michael; Brighina, Laura; Spitz, Mariana; Suchowersky, Oksana; Riess, Olaf; Das, Parimal; Mollenhauer, Brit; Gatto, Emilia M.; Petersen, Maria Skaalum; Hattori, Nobutaka; Wu, Ruey-Meei; Illarioshkin, Sergey N.; Valente, Enza Maria; Aasly, Jan O.; Aasly, Anna; Alcalay, Roy N.; Thaler, Avner; Farrer, Matthew J.; Brockmann, Kathrin; Corvol, Jean-Christophe; Klein, Christine

A Novel AQP2 Sequence Variant Causing Aquaporin-2 Retention in the Cytoplasm and Autosomal Dominant Nephrogenic Diabetes Insipidus

KIDNEY INTERNATIONAL REPORTS

IF5.7

2022-10-01

OAAI

Hinrichs, Gitte R.; Baltzer, Sandrine; Pallien, Tamara; Svenningsen, Per; Dalgaard, Emil B.; Hertz, Jens Michael; Bistrup, Claus; Jensen, Boye L.; Klussmann, Enno

Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2021-04-15

OAAI

Savige, Judy; Storey, Helen; Watson, Elizabeth; Hertz, Jens Michael; Deltas, Constantinos; Renieri, Alessandra; Mari, Francesca; Hilbert, Pascale; Plevova, Pavlina; Byers, Peter; Cerkauskaite, Agne; Gregory, Martin; Cerkauskiene, Rimante; Ljubanovic, Danica Galesic; Becherucci, Francesca; Errichiello, Carmela; Massella, Laura; Aiello, Valeria; Lennon, Rachel; Hopkinson, Louise; Koziell, Ania; Lungu, Adrian; Rothe, Hansjorg Martin; Hoefele, Julia; Zacchia, Miriam; Martic, Tamara Nikuseva; Gupta, Asheeta; van Eerde, Albertien; Gear, Susie; Landini, Samuela; Palazzo, Viviana; Al-Rabadi, Laith; Claes, Kathleen; Corveleyn, Anniek; Van Hoof, Evelien; van Geel, Micheel; Williams, Maggie; Ashton, Emma; Belge, Hendica; Ars, Elisabeth; Bierzynska, Agnieszka; Gangemi, Concetta; Lipska-Zietkiewicz, Beata S.

Skewness of X-chromosome inactivation increases with age and varies across birth cohorts in elderly Danish women

SCIENTIFIC REPORTS

IF3.9

2021-02-22

OAAI

Mengel-From, Jonas; Lindahl-Jacobsen, Rune; Nygaard, Marianne; Soerensen, Mette; Orstavik, Karen Helene; Hertz, Jens Michael; Andersen-Ranberg, Karen; Tan, Qihua; Christensen, Kaare

Expanding the cerebrovascular phenotype of the p.R258H variant in ACTA2 related hereditary thoracic aortic disease (HTAD)

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2020-08-01

PREAI

Diness, Birgitte Rode; Palmquist, Rachel Nina; Norling, Rikke; Hove, Hanne; Bundgaard, Henning; Hertz, Jens Michael; Kondziella, Daniel; Krieger, Derk; Duno, Morten; Gronborg, Sabine

DNA hypermethylation and differential gene expression associated with Klinefelter syndrome

SCIENTIFIC REPORTS

IF3.9

2018-09-13

OAAI

Skakkebaek, Anne; Nielsen, Morten Muhlig; Trolle, Christian; Vang, Soren; Hornshoj, Henrik; Hedegaard, Jakob; Wallentin, Mikkel; Bojesen, Anders; Hertz, Jens Michael; Fedder, Jens; Ostergaard, John Rosendahl; Pedersen, Jakob Skou; Gravholt, Claus Hojbjerg

Properties and units in the clinical laboratory sciences part XXIV. Properties and units in clinical molecular genetics (technical report 2017)

CLINICA CHIMICA ACTA

IF2.9

2018-09-01

PREAI

Petersen, Ulla M.; Padro-Miquel, Ariadna; Taylor, Graham; Hertz, Jens Michael; Ceder, Rebecca; Fuentes-Arderiu, Xavier; den Dunnen, Johan T.

Hereditary spastic paraplegia type 8: Neuropathological findings

BRAIN PATHOLOGY

IF6.2

2018-03-08

OAAI

Pehrson, Caroline; Hertz, Jens Michael; Wirenfeldt, Martin; Stenager, Egon; Wermuth, Lene; Kristensen, Bjarne Winther

Ichthyosis with Confetti Inherited from a Mosaic Father

ACTA DERMATO-VENEREOLOGICA

IF3.7

2018-01-01

OAAI

Pallesen, Kristine A. U.; Clemmensen, Ole; Fischer, Judith; Hertz, Jens Michael; Bygum, Anette

DOK7 congenital myasthenia may be associated with severe mitral valve insufficiency

JOURNAL OF THE NEUROLOGICAL SCIENCES

IF3.2

2017-08-01

PREAI

Gaist, David; Mogensen, Jens; Pedersen, Emil Greve; Schroder, Henrik Daa; Vissing, John; Andersen, Henning; Hertz, Jens Michael

A Gene Implicated in Activation of Retinoic Acid Receptor Targets Is a Novel Renal Agenesis Gene in Humans

GENETICS

IF5.1

2017-07-26

OAAI

Brophy, Patrick D.; Rasmussen, Maria; Parida, Mrutyunjaya; Bonde, Greg; Darbro, Benjamin W.; Hong, Xiaojing; Clarke, Jason C.; Peterson, Kevin A.; Denegre, James; Schneider, Michael; Sussman, Caroline R.; Sunde, Lone; Lildballe, Dorte L.; Hertz, Jens Michael; Cornell, Robert A.; Murray, Stephen A.; Manak, J. Robert

Moebius sequence -a multidisciplinary clinical approach

ORPHANET JOURNAL OF RARE DISEASES

IF3.5

2017-01-06

OAAI

Pedersen, Line Kjeldgaard; Maimburg, Rikke Damkjaer; Hertz, Jens Michael; Gjorup, Hans; Pedersen, Thomas Klit; Moller-Madsen, Bjarne; Ostergaard, John Rosendahl

Neuroanatomical correlates of Klinefelter syndrome studied in relation to the neuropsychological profile (vol 4, pg 1, 2014)

NEUROIMAGE-CLINICAL

IF3.6

2016-01-01

OAAI

Skakkebaek, Anne; Gravholt, Claus Hojbjerg; Rasmussen, PeterMondrup; Bojesen, Anders; Jensen, Jens Sondergaard; Fedder, Jens; Laurberg, Peter; Hertz, Jens Michael; Ostergaard, John Rosendahl; Pedersen, Anders Degn; Wallentin, Mikkel

Klinefelter syndrome has increased brain responses to auditory stimuli and motor output, but not to visual stimuli or Stroop adaptation

NEUROIMAGE-CLINICAL

IF3.6

2016-01-01

OAAI

Wallentin, Mikkel; Skakkebaek, Anne; Bojesen, Anders; Fedder, Jens; Laurberg, Peter; Ostergaard, John R.; Hertz, Jens Michael; Pedersen, Anders Degn; Gravholt, Claus Hojbjerg

研究方向