1. The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease. 
Yépez VA, Demidov G, Ellwanger K, Laurie S, Luknárová R, Joseph Maran MI, Hentrich T,  Sagath L, van der Sanden B, Astuti G, Neveling K, Batlle-Masó L, Beijer D, Brechtmann F,  Caballero-Oteyza A, Dabad M, Denommé-Pichon AS, Doornbos C, Eddafir Z, Estévez-Arias B,  Kilicarslan OA, Kolen IHM, Kraß L, Lohmann K, Londhe S, López-Martín E, Maassen K, Macken W, Martínez-Delgado B, Mei D, Mertes C, Minardi R, Morsy H, Mueller JS, Natera-de Benito D, Nelson I, Oud MM, Paramonov I, Picó D, Piscia D, Polavarapu K, Raineri E, Savarese M, Smal N, Steehouwer M, Steyaert W, Swertz MA, Thomsen M, Töpf A, Van de Vondel L, van der Vries 
G, Vitobello A, Wilke C, Zurek B; Solve-RD DITF-EPICARE; Solve-RD DITF-ITHACA; Solve-RD DITF-EURO-NMD; Solve-RD DITF-RITA; Solve-RD DITF-RND; Solve-RD consortium; T' Hoen PB, Matalonga L, Vissers LELM, Gilissen C, Schulze-Hentrich J, Beltran S, Esteve-Codina A, Hoischen A, Gagneur J, Graessner H.
Nat Genet. 2025 Sep 9. doi: https://doi.org/10.1038/s41588-025-02290-3. Online ahead of print. PMID: https://pubmed.ncbi.nlm.nih.gov/40926087 Review. 

2. Heterozygous Missense Variants in the ATPase Phospholipid Transporting 9A Gene, ATP9A, Alter Dendritic Spine Maturation and Cause Dominantly Inherited Nonsyndromic Intellectual Disability. 
Cordovado A, Hérenger Y, Cormier C, López-Martín E, Stamberger H, Faivre L, DenomméPichon AS, Vitobello A, Abdallah HH, Barcia G, Courtin T, Martínez-Delgado B, BermejoSánchez E, Barrero MJ, Gasser B, Bezieau S, Küry S, Weckhuysen S, Laumonnier F, Toutain A,  Vuillaume ML.
Hum Mutat. 2025 Mar 5;2025:7085599. doi: https://doi.org/10.1155/humu/7085599. eCollection 2025. PMID: https://pubmed.ncbi.nlm.nih.gov/40226306 Free PMC article.

3. Mosaicism and intronic variants in RB1 gene revealed by next generation sequencing in a cohort of Spanish retinoblastoma  patients. 
Gomez-Mariano G, Hernandez-SanMiguel E, Fernandez-Prieto M, Ramos Del Saz S, Baladrón B, Mielu LM, Rivera D, Moneo V, Lopez L, Rodriguez-Martin C, Fernandez-Teijeiro Álvarez A, Sabado C, Bermejo E, Alonso FJ, Martinez-Delgado B.
Exp Eye Res. 2025 Feb;251:110233. doi: https://doi.org/10.1016/j.exer.2025.110233. Epub 2025 Jan 6. PMID:  https://pubmed.ncbi.nlm.nih.gov/39778672 

4. EHMT2 as a Candidate Gene for an Autosomal Recessive Neurodevelopmental Syndrome. 
Carvalho LML, Rzasa J, Kerkhof J, McConkey H, Fishman V, Koksharova G, de Lima Jorge AA, Branco EV, de Oliveira DF, Martinez-Delgado B, Barrero MJ, Kleefstra T, Sadikovic B, Haddad LA, Bertola DR, Rosenberg C, Krepischi ACV.
Mol Neurobiol. 2025 May;62(5):5977-5989. doi: https://doi.org/10.1007/s12035-024-04655-x. Epub 2024 Dec 15. PMID: https://pubmed.ncbi.nlm.nih.gov/39674972 

5. Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant. 
Komulainen-Ebrahim J, Kangas SM, López-Martín E, Feyma T, Scaglia F, Martínez-Delgado B, Kuismin O, Suo-Palosaari M, Carr L, Hinttala R, Kurian MA, Uusimaa J. Mov Disord Clin Pract. 2024 Jun;11(6):708-715. doi: https://doi.org/10.1002/mdc3.14051. Epub 2024 May 2. PMID: https://pubmed.ncbi.nlm.nih.gov/38698576 Free PMC article.

6. CERT1 mutations perturb human development by disrupting sphingolipid homeostasis. 
Gehin C, Lone MA, Lee W, Capolupo L, Ho S, Adeyemi AM, Gerkes EH, Stegmann AP, LópezMartín E, Bermejo-Sánchez E, Martínez-Delgado B, Zweier C, Kraus C, Popp B, Strehlow V, Gräfe D, Knerr I, Jones ER, Zamuner S, Abriata LA, Kunnathully V, Moeller BE, Vocat A,  Rommelaere S, Bocquete JP, Ruchti E, Limoni G, Van Campenhoudt M, Bourgeat S, Henklein P, Gilissen C, van Bon BW, Pfundt R, Willemsen MH, Schieving JH, Leonardi E, Soli F, Murgia A, Guo H, Zhang Q, Xia K, Fagerberg CR, Beier CP, Larsen MJ, Valenzuela I, Fernández-Álvarez P, Xiong S, Śmigiel R, López-González V, Armengol L, Morleo M, Selicorni A, Torella A, Blyth M, Cooper NS, Wilson V, Oegema R, Herenger Y, Garde A, Bruel AL, Tran Mau-Them F, Maddocks AB, Bain JM, Bhat MA, Costain G, Kannu P, Marwaha A, Champaigne NL, Friez MJ, Richardson EB, Gowda VK, Srinivasan VM, Gupta Y, Lim TY, Sanna-Cherchi S, Lemaitre B, Yamaji T, 
Hanada K, Burke JE, Jakšić AM, McCabe BD, De Los Rios P, Hornemann T, D'Angelo G,  Gennarino VA. J Clin Invest. 2023 May 15;133(10):e165019. doi: https://doi.org/10.1172/JCI165019. PMID: https://pubmed.ncbi.nlm.nih.gov/36976648 Free PMC article.

7. Differences in Expression of IQSEC2 Transcript Isoforms in Male and Female Cases with Loss of Function Variants and  Neurodevelopmental Disorder. 
Baladron B, Mielu LM, López-Martín E, Barrero MJ, Lopez L, Alvarado JI, Monzón S, Varona S, Cuesta I, Cazorla R, Lara J, Iglesias G, Román E, Ros P, Gomez-Mariano G, Cubillo I, Miguel EH, Rivera D, Alonso J, Bermejo-Sánchez E, Posada M, Martínez-Delgado B.
Int J Mol Sci. 2022 Aug 22;23(16):9480. doi: https://doi.org/10.3390/ijms23169480. PMID: https://pubmed.ncbi.nlm.nih.gov/36012761 Free PMC article.

8. Epigenomic Approaches for the Diagnosis of Rare Diseases. 
Martinez-Delgado B, Barrero MJ. Epigenomes. 2022 Jul 27;6(3):21. doi: https://doi.org/10.3390/epigenomes6030021. PMID: https://pubmed.ncbi.nlm.nih.gov/35997367 Free PMC article. Review. 

9. miR-320c Regulates SERPINA1 Expression and Is Induced in Patients With Pulmonary Disease. 
Matamala N, Lara B, Gómez-Mariano G, Martínez S, Vázquez-Domínguez I, Otero-Sobrino Á, Muñoz-Callejas A, Sánchez E, Esquinas C, Bustamante A, Cadenas S, Curi S, Lázaro L, Martínez MT, Rodríguez E, Miravitlles M, Torres-Duran M, Herrero I, Michel FJ, Castillo S, Hernández-Pérez JM, Blanco I, Casas F, Martínez-Delgado B.Arch Bronconeumol. 2021 Jul;57(7):457-463. doi: https://doi.org/10.1016/j.arbr.2020.03.031. PMID: https://pubmed.ncbi.nlm.nih.gov/35698951 

10. CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative. 
Luque J, Mendes I, Gómez B, Morte B, López de Heredia M, Herreras E, Corrochano V, Bueren J, Gallano P, Artuch R, Fillat C, Pérez-Jurado LA, Montoliu L, Carracedo Á, Millán JM, Webb SM, Palau F; CIBERER Network; Lapunzina P. Clin Genet. 2022 May;101(5-6):481-493. doi: https://doi.org/10.1111/cge.14113. Epub 2022 Feb 4. PMID: https://pubmed.ncbi.nlm.nih.gov/35060122 Free PMC article. Review. 

11. De novo small deletion affecting transcription start site of short isoform of AUTS2 gene in a patient with syndromic neurodevelopmental defects. 
Martinez-Delgado B, Lopez-Martin E, Lara-Herguedas J, Monzon S, Cuesta I, Juliá M, Aquino V, Rodriguez-Martin C, Damian A, Gonzalo I, Gomez-Mariano G, Baladron B, Cazorla R, Iglesias G, Roman E, Ros P, Tutor P, Mellor S, Jimenez C, Cabrejas MJ, Gonzalez-Vioque E, Alonso J, Bermejo-Sánchez E, Posada M. Am J Med Genet A. 2021 Mar;185(3):877-883. doi: https://doi.org/10.1002/ajmg.a.62017. Epub 2020 Dec 21. PMID: https://pubmed.ncbi.nlm.nih.gov/33346930 

12. New cis-Acting Variants in PI*S Background Produce Null Phenotypes Causing Alpha-1 Antitrypsin Deficiency. 
Matamala N, Gomez-Mariano G, Perez JA, Baladrón B, Torres-Durán M, Michel FJ, Saez R, Hernández-Pérez JM, Belmonte I, Rodriguez-Frias F, Blanco I, Strnad P, Janciauskiene S, Martinez-Delgado B. Am J Respir Cell Mol Biol. 2020 Oct;63(4):444-451. doi: https://doi.org/10.1165/rcmb.2020-0021OC. PMID: https://pubmed.ncbi.nlm.nih.gov/32515985 

13. Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum. 
Urreizti R, Lopez-Martin E, Martinez-Monseny A, Pujadas M, Castilla-Vallmanya L, PérezJurado LA, Serrano M, Natera-de Benito D, Martínez-Delgado B, Posada-de-la-Paz M, Alonso J, Marin-Reina P, O'Callaghan M, Grinberg D, Bermejo-Sánchez E, Balcells S.
Orphanet J Rare Dis. 2020 Feb 10;15(1):44. doi: https:/doi.org/10.1186/s13023-020-1317-9. PMID: https://pubmed.ncbi.nlm.nih.gov/32041641 Free PMC article.

14. SpainUDP: The Spanish Undiagnosed Rare Diseases Program. 
López-Martín E, Martínez-Delgado B, Bermejo-Sánchez E, Alonso J; SpainUDP Network; Posada M. Int J Environ Res Public Health. 2018 Aug 14;15(8):1746. doi: https://doi.org/10.3390/ijerph15081746. PMID: https://pubmed.ncbi.nlm.nih.gov/30110963 Free PMC article.

15. Characterization of Novel Missense Variants of SERPINA1 Gene Causing Alpha-1 Antitrypsin Deficiency. 
Matamala N, Lara B, Gomez-Mariano G, Martínez S, Retana D, Fernandez T, Silvestre RA, Belmonte I, Rodriguez-Frias F, Vilar M, Sáez R, Iturbe I, Castillo S, Molina-Molina M, Texido A, Tirado-Conde G, Lopez-Campos JL, Posada M, Blanco I, Janciauskiene S, Martinez-Delgado B. Am J Respir Cell Mol Biol. 2018 Jun;58(6):706-716. doi: https://doi.org/10.1165/rcmb.2017-0179OC. PMID: https://pubmed.ncbi.nlm.nih.gov/29232161 

16. Identification of genetic variants in pharmacokinetic genes associated with Ewing Sarcoma treatment outcome.
Ruiz-Pinto S, Pita G, Patiño-García A, García-Miguel P, Alonso J, Pérez-Martínez A, Sastre A, Gómez-Mariano G, Lissat A, Scotlandi K, Serra M, Ladenstein R, Lapouble E, Pierron G, Kontny U, Picci P, Kovar H, Delattre O, González-Neira A.Ann Oncol. 2016 Sep;27(9):1788-93. doi: https://doi.org/10.1093/annonc/mdw234. Epub 2016 Jun 10. PMID: https://pubmed.ncbi.nlm.nih.gov/27287205 Free article.

17. Familial retinoblastoma due to intronic LINE-1 insertion causes aberrant and noncanonical mRNA splicing of the RB1 gene.
Rodríguez-Martín C, Cidre F, Fernández-Teijeiro A, Gómez-Mariano G, de la Vega L, Ramos P, Zaballos Á, Monzón S, Alonso J.
J Hum Genet. 2016 May;61(5):463-6. doi: https://doi.org/10.1038/jhg.2015.173. Epub 2016 Jan 14. PMID: https://pubmed.ncbi.nlm.nih.gov/26763876

18. Low penetrance hereditary retinoblastoma in a family: what should we consider in the genetic counselling process and follow up?
Serrano C, Alonso J, Gómez-Mariano G, Aguirre E, Diez O, Gadea N, Bosch N, Balmaña J, Graña B.Fam Cancer. 2011 Sep;10(3):617-21. doi: https://doi.org/10.1007/s10689-011-9445-y. PMID: https://pubmed.ncbi.nlm.nih.gov/21538077

19. Spanish Registry of Patients With Alpha-1 Antitrypsin Deficiency: Database Evaluation and Population Analysis. 
Lara B, Blanco I, Martínez MT, Rodríguez E, Bustamante A, Casas F, Cadenas S, Hernández JM, Lázaro L, Torres M, Curi S, Esquinas C, Dasí F, Escribano A, Herrero I, Martínez-Delgado B, Michel FJ, Rodríguez-Frías F, Miravitlles M. Arch Bronconeumol. 2017 Jan;53(1):13-18. doi: https://doi.org/10.1016/j.arbres.2016.05.003. Epub 2016 Jun 17. PMID: https://pubmed.ncbi.nlm.nih.gov/27323654 English, Spanish. 

20. Severe alpha-1 antitrypsin deficiency in composite heterozygotes inheriting a new splicing mutation QOMadrid. 
Lara B, Martínez MT, Blanco I, Hernández-Moro C, Velasco EA, Ferrarotti I, Rodriguez-Frias F, Perez L, Vazquez I, Alonso J, Posada M, Martínez-Delgado B. Respir Res. 2014 Oct 7;15(1):125. doi: https://doi.org/10.1186/s12931-014-0125-y. PMID: https://pubmed.ncbi.nlm.nih.gov/25287719 Free PMC article