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Verloes Alain

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Main Referenced Co-authors
Koulischer, Lucien  (19)
Herens, Christian  (17)
Misson, Jean-Paul  (11)
Beckers, Albert  (10)
Van Maldergem, Lionel  (10)
Main Referenced Keywords
Humans (13); Male (11); Female (10); Adult (5); Middle Aged (5);
Main Referenced Disciplines
Genetics & genetic processes (26)
Endocrinology, metabolism & nutrition (13)
Pediatrics (11)
Neurology (10)
Surgery (6)

Publications (total 60)

The most downloaded
746 downloads
Gusbin, N., Verloes, A., Daly, A., & Beckers, A. (July 2006). Les grandes tailles: quelques grands syndromes et revue de la litterature. Revue Médicale de Liège, 61 (7-8, Jul-Aug), 572-80. https://hdl.handle.net/2268/23318

The most cited

182 citations (Scopus®)

VERLOES, A., SakalihasanN, N., Koulischer, L., & Limet, R. (1995). Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees. Journal of Vascular Surgery, 21 (4), 646-55. doi:10.1016/S0741-5214(95)70196-6 https://hdl.handle.net/2268/109710

Ruaud, L., Drunat, S., Elmaleh-Bergès, M., Ernault, A., Guilmin Crepon, S., MCPH Consortium, El Ghouzzi, V., Auvin, S., Verloes, A., Passemard, S., Servais, L., & VAESSEN, S. (April 2022). Neurological outcome in WDR62 primary microcephaly. Developmental Medicine and Child Neurology, 64 (4), 509-517. doi:10.1111/dmcn.15060
Peer Reviewed verified by ORBi

VALDES SOCIN, H. G., VERLOES, A., Debray, F.-G., LIBIOULLE, C., Pintiaux, A., Maquet, P., & Beckers, A. (2016). Le syndrome de De Morsier : une cause congénitale méconnue d'hypopituitarisme. In Annales d'Endocrinologie : 33ème congrès de la Société Française d'Endocrinologie.

JACQUINET, A., VALDES SOCIN, H. G., LIBIOULLE, C., CABERG, J.-H., & VERLOES, A. (22 October 2013). Femoral-facial syndrome: long term follow-up and associated array CGH abnormalities [Poster presentation]. American Society of Human Genetics 63rd Annual Meeting, Boston, United States.

COTTEREAU,, E., MORTEMOUSQUE, I., MOIZARD, M.-P., BÜRGLEN, L., LACOMBE, D., GILBERT‐DUSSARDIER, B., SIGAUDY, S., BOUTE, O., DAVID, A., FAIVRE, L., AMIEL, J., ROBERTSON, R., VIANA RAMOS, F., BIETH, E., ODENT, S., DEMEER, B., MATHIEU, M., GAILLARD, D., VAN MALDERGEM, L., ... TOUTAIN, A. (May 2013). Phenotypic Spectrum of Simpson–Golabi– Behmel Syndrome in a Series of 42 Cases With a Mutation in GPC3 and Review of the Literature. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 163C (2), 92-105. doi:10.1002/ajmg.c.31360
Peer reviewed

Jacquinet, A., Gerard, M., Gabbett, M. T., Rausin, L., Misson, J.-P., Menten, B., Mortier, G., Van Maldergem, L., Verloes, A., & Debray, F.-G. (2010). Temple-Baraitser syndrome: a rare and possibly unrecognized condition. American Journal of Medical Genetics. Part A, 152A (9), 2322-6. doi:10.1002/ajmg.a.33574
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Hilton, E., Johnston, J., Whalen, S., Okamoto, N., Hatsukawa, Y., Nishio, J., Kohara, H., Hirano, Y., Mizuno, S., Torii, C., Kosaki, K., Manouvrier, S., Boute, O., Perveen, R., Law, C., Moore, A., Fitzpatrick, D., Lemke, J., Fellmann, F., ... Black, G. (2009). BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects. European Journal of Human Genetics, 17 (10), 1325-35. doi:10.1038/ejhg.2009.52
Peer Reviewed verified by ORBi

Mutesa, L., Hellin, A.-C., Jamar, M., Pierquin, G., Bours, V., & Verloes, A. (2007). Precocious puberty associated with partial trisomy 18q and monosomy 11q. Genetic Counseling, 18 (2), 201-207.
Peer Reviewed verified by ORBi

Gusbin, N., Verloes, A., Daly, A., & Beckers, A. (July 2006). Les grandes tailles: quelques grands syndromes et revue de la litterature. Revue Médicale de Liège, 61 (7-8, Jul-Aug), 572-80.
Peer reviewed

Blaise, P., Fumal, A., Janin, N., Verloes, A., Moonen, G., & Andris, C. (February 2005). Diffuse cortical atrophy in a patient with Turner syndrome and Leber hereditary optic neuropathy. Journal of Neurology, 252 (2), 232-233. doi:10.1007/s00415-005-0615-4
Peer Reviewed verified by ORBi

Lado-Abeal, J., DUMITRESCU, A., LIAO, X.-H., COHEN, R., POHLENZ, J., WEISS, R., LEBRETHON, M.-C., VERLOES, A., & REFETOFF, S. (2005). A De Novo Mutation in an Already Mutant Nucleotide of the Thyroïd Hormone Receptor beta Gene Perpetuates Resistance to Thyroid Hormone. Journal of Clinical Endocrinology and Metabolism, 90 (3), 1760-1767. doi:10.1210/jc.2004-1488
Peer Reviewed verified by ORBi

Verloes, A., Raoul, M., Genevieve, D., Sznajer, Y., Demarche, M., Lombet, J., Rigo, V., Misson, J.-P., Collignon, L., Vanwijck, F., & Vanwijck, R. (October 2004). Bony syngnathia, vertebral segmentation defect, coloboma, microcephaly and mental retardation: confirmation of Dobrow syndrome and review of syndromal syngnathias. Clinical Dysmorphology, 13 (4), 205-211. doi:10.1097/00019605-200410000-00002
Peer Reviewed verified by ORBi

Verloes, A., Massin, M., Fransolet, A.-C., & Misson, J.-P. (2004). Hypertrichosis, fallot tetralogy, growth and developmental delay. Clinical Dysmorphology, 13, 247-250. doi:10.1097/00019605-200410000-00009
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Shibamura, H., Olson, J. M., van Vlijmen-Van Keulen, C., Buxbaum, S. G., Dudek, D. M., Tromp, G., Ogata, T., Skunca, M., SakalihasanN, N., Pals, G., Limet, R., MacKean, G. L., Defawe, O., VERLOES, A., Arthur, C., Lossing, A. G., Burnett, M., Sueda, T., & Kuivaniemi, H. (2004). Genome scan for familial abdominal aortic aneurysm using sex and family history as covariates suggests genetic heterogeneity and identifies linkage to chromosome 19q13. Circulation, 109 (17), 2103-8. doi:10.1161/01.CIR.0000127857.77161.A1
Peer Reviewed verified by ORBi

Rodriguez, L., Guardia, N. M., Herens, C., Jamar, M., Verloes, A., Lopez, F., Munoz, J. S., & Martinez-Frias, M. L. (01 October 2003). Subtle trisomy 12q24.3 and subtle monosomy 22q13.3: Three new cases and review [letter to the editor]. American Journal of Medical Genetics. Part A, 122A (2), 119-124. doi:10.1002/ajmg.a.20243
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Kuivaniemi, H., Shibamura, H., Arthur, C., Berguer, R., Cole, C. W., Juvonen, T., Kline, R. A., Limet, R., Mackean, G., Norrgard, O., Pals, G., Powell, J. T., Rainio, P., SakalihasanN, N., van Vlijmen-van Keulen, C., VERLOES, A., & Tromp, G. (2003). Familial abdominal aortic aneurysms: collection of 233 multiplex families. Journal of Vascular Surgery, 37 (2), 340-5. doi:10.1067/mva.2003.71
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Shibamura, H., Buxbaum, S., Olson, J. M., Tromp, G., Skunca, M., Arthur, C., Berguer, R., Cole, C. W., Limet, R., MacKean, G., Pals, G., Sakalihasan, N., van Vlijmen-van Keulen, C., Verloes, A., & Kuivaniemi, H. (2002). Candidate locus for familial abdominal aortic aneurysms by genome-wide DNA linkage analysis. Circulation, 106 (19, Suppl. S), 168.
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Verloes, A., JAMAR, M., Dideberg, V., & Herens, C. (2001). Episphalosomic Syndrome : A Mca Syndrome Ressembling Fanconi Anemia, with Increased Baseline Level of Chromosome Breaks but No Hypersensivity to Clastogens. Annales de Génétique, 44 (2, Apr-Jun), 59-62. doi:10.1016/S0003-3995(01)01043-7
Peer Reviewed verified by ORBi

Verloes, A., Gillerot, Y., Van Maldergem, L., Schoos, R., Herens, C., Jamar, M., Dideberg, V., Lesenfants, S., & Koulischer, L. (January 2001). Major Decrease in the Incidence of Trisomy 21 at Birth in South Belgium: Mass Impact of Triple Test? European Journal of Human Genetics, 9 (1), 1-4. doi:10.1038/sj.ejhg.5200575
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Verloes, A., Hermanns-Le, T., Lesenfants, S., Lombet, J., Lamotte, P. J., Crevecoeur-Liegeois, C., Duchesne, B., & Pierard, G. (29 October 1999). Koraxitrachitic Syndrome: A Syndromic Form of Self-Healing Collodion Baby with Residual Dappled Atrophy of the Derma. American Journal of Medical Genetics, 86 (5), 454-8. doi:10.1002/(SICI)1096-8628(19991029)86:5<454::AID-AJMG11>3.0.CO;2-U
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Verloes, A., Stevenaert, A., Teh, B. T., Petrossians, P., & Beckers, A. (May 1999). Familial Acromegaly: Case Report and Review of the Literature. Pituitary, 1 (3-4), 273-277. doi:10.1023/A:1009958510378
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Wang, X., Tromp, G., Cole, C. W., VERLOES, A., SakalihasanN, N., Yoon, S., & Kuivaniemi, H. (1999). Analysis of coding sequences for tissue inhibitor of metalloproteinases 1 (TIMP1) and 2 (TIMP2) in patients with aneurysms. Matrix Biology, 18 (2), 121-4. doi:10.1016/S0945-053X(99)00008-6
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Poncin, J., Abs, R., Velkeniers, B., Bonduelle, M., Abramowicz, M., Legros, J.-J., Verloes, A., Meurisse, M., Van Gaal, L., Verellen, C., Koulischer, L., & Beckers, A. (1999). Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases. Human Mutation, 13 (1), 54-60. doi:10.1002/(SICI)1098-1004(1999)13:1<54::AID-HUMU6>3.0.CO;2-K
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Beckers, A., Stevenaert, A., Teh, B. T., Petrossians, P., & Verloes, A. (1999). Familial Acromegaly : Case report and review of the litterature. In The 6th International Pituitary Congress - Abstract book (pp. 68).

Verloes, A., Curry, C., Jamar, M., Herens, C., O'Lague, P., Marks, J., Sarda, P., & Blanchet, P. (November 1998). Juvenile Rheumatoid Arthritis and Del(22q11) Syndrome: A Non-Random Association. Journal of Medical Genetics, 35 (11), 943-7. doi:10.1136/jmg.35.11.943
Peer Reviewed verified by ORBi

Schoos, R., Verloes, A., Bourguignon, J.-P., & Koulischer, L. (May 1998). Les programmes de dépistage systématique en néonatologie. Aspects pharmaco-économiques. Revue Médicale de Liège, 53 (5), 311-5.
Peer reviewed

Limet, R., Nusgens, B., VERLOES, A., & Sakalihasan, N. (1998). Pathogenesis of abdominal aortic aneurysm (AAA) formation. Acta Chirurgica Belgica, 98 (5), 195-8.
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Marquet, F., Verloes, A., & Beckers, A. (1998). Le cas clinique du mois Un homme a caryotype 46,XX. Revue Médicale de Liège, 53 (9), 515-517.
Peer reviewed

Marquet, F., Beckers, A., & Verloes, A. (1998). Aspects genetiques du male 46, XX. Revue Médicale de Liège, 53 (12), 738-740.
Peer reviewed

Poncin, J., Abs, R., Velkeniers, B., Bonduelle, M., Abramowicz, M., Legros, J.-J., Verloes, A., Van gaal, L., Koulischer, L., & Beckers, A. (1998). Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type I and related diseases. In IV european Congress of Endocrinology - Abstract book.

Van Coster, Janssens, S., Misson, J.-P., Verloes, A., & Leroy, J. (1998). Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples. Prenatal Diagnosis, 18, 1041-1044. doi:10.1002/(SICI)1097-0223(1998100)18:10<1041::AID-PD407>3.0.CO;2-J
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Poncin, J., Abs, R., Velkeniers, B., Bonduelle, M., Abramowicz, M., Legros, J.-J., Verloes, A., Meurisse, M., Van Gaal, L., Koulischer, L., & Beckers, A. (1998). Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type I and related diseases. In 5th Euroregional Oncology meeting - abstract book.

Herens, C., Jamar, M., Alvarez Gonzalez, M.-L., Lesenfants, S., Lombet, J., Bonnivert, J., Koulischer, L., & Verloes, A. (12 December 1997). Private Multiple Congenital Anomaly Syndromes May Result from Unbalanced Subtle Translocations: T(2q;4p) Explains the Lambotte Syndrome. American Journal of Medical Genetics, 73 (2), 127-31. doi:10.1002/(SICI)1096-8628(19971212)73:2<127::AID-AJMG5>3.0.CO;2-R
Peer Reviewed verified by ORBi

Koulischer, L., Verloes, A., Lesenfants, S., Jamar, M., & Herens, C. (September 1997). Genetic Risk in Natural and Medically Assisted Procreation. Early Pregnancy: Biology and Medicine, 3 (3), 164-71.
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Verloes, A., Lesenfants, S., Misson, J.-P., Galand, A., & Koulischer, L. (10 February 1997). Microcephaly, muscular build, rhizomelia, and cataracts: Description of a possible recessive syndrome and some comments on the use of electronic databases in syndromology. American Journal of Medical Genetics, 68 (4), 455-60, discussion 461. doi:10.1002/(SICI)1096-8628(19970211)68:4<455::AID-AJMG16>3.0.CO;2-R
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Janssens, S., Van Coster, R., Chang, J., Raes, F., Misson, J.-P., & Verloes, A. (1997). Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples. European Journal of Paediatric Neurology, 1, 105.
Peer Reviewed verified by ORBi

VERLOES, A., Sakalihasan, N., Limet, R., & Koulischer, L. (1996). Genetic aspects of abdominal aortic aneurysm. Annals of the New York Academy of Sciences, 800, 44-55. doi:10.1111/j.1749-6632.1996.tb33297.x
Peer Reviewed verified by ORBi

Verloes, A., Jamblin, P., Koulischer, L., & Bourguignon, J.-P. (January 1996). A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondyly. Clinical Genetics, 49 (1), 2-5. doi:10.1111/j.1399-0004.1996.tb04315.x
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Ectors, F., Koulischer, L., JAMAR, M., HERENS, C., VERLOES, A., Remy, B., & Beckers, J.-F. (August 1995). Cytogenetic study of bovine oocytes matured in vitro. Theriogenology, 44 (3), 445-450. doi:10.1016/0093-691X(95)00198-H
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Verloes, A., Misson, J.-P., Dubru, J. M., Jamblin, P., & Le Merrer, M. (July 1995). Heterogeneity of sponastrime dysplasia: Delineation of a variant form with severe mental retardation. Clinical Dysmorphology, 4 (3), 208-215.
Peer Reviewed verified by ORBi

Verloes, A., Schoos, R., Herens, C., Vintens, A., & Koulischer, L. (January 1995). A Prenatal Trisomy 21 Screening Program Using Alpha-Fetoprotein, Human Chorionic Gonadotropin, and Free Estriol Assays on Maternal Dried Blood. American Journal of Obstetrics and Gynecology, 172 (1, Pt 1), 167-74. doi:10.1016/0002-9378(95)90108-6
Peer Reviewed verified by ORBi

Misson, J.-P., Lombet, J., Rigo, J., Verloes, A., Weerts, E., & Van Coster, R. (1995). Caractéristiques neuroradiologiques du déficit en Pyruvate Carboxylase. In Société Européenne de Neurologie Pédiatrique.
Peer reviewed

VERLOES, A., SakalihasanN, N., Koulischer, L., & Limet, R. (1995). Aneurysms of the abdominal aorta: familial and genetic aspects in three hundred thirteen pedigrees. Journal of Vascular Surgery, 21 (4), 646-55. doi:10.1016/S0741-5214(95)70196-6
Peer Reviewed verified by ORBi

Verloes, A., Beckers, A., Pétrossians, E., & Stevenaert, A. (1994). Familial aspects in acromegaly. In 26th Annual meeting of European society of Human Genetics. Abstract book.

Hustinx, R., Verloes, A., Grattagliano, B., Herens, C., Jamar, M., Soyeur, D., Schaaps, J.-P., & Koulischer, L. (01 September 1993). Monosomy 11q: Report of Two Familial Cases and Review of the Literature. American Journal of Medical Genetics, 47 (3), 312-7. doi:10.1002/ajmg.1320470303
Peer Reviewed verified by ORBi

Verloes, A., Journel, H., Elmer, C., Misson, J.-P., Le Merrer, M., Kaplan, J., Van Maldergem, L., Deconinck, H., & Meire, F. (15 April 1993). Heterogeneity versus variability in Neuhauser megalocornea-mental retardation (MMR) syndromes: Report of new cases and delineation of 4 probable types. American Journal of Medical Genetics, 46 (2), 132-137. doi:10.1002/ajmg.1320460206
Peer Reviewed verified by ORBi

Verloes, A., Bonneau, D., Guidi, O., Berthier, M., Oriot, D., Van Maldergem, L., & Koulischer, L. (February 1993). Brachymorphism-Onychodysplasia-Dysphalangism Syndrome. Journal of Medical Genetics, 30 (2), 158-61. doi:10.1136/jmg.30.2.158
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Leroy, P., Verloes, A., Born, J., Pierrard, A., Otto, B., & Misson, J.-P. (1993). Syndrome oculo-cérébro-cutané de Delleman. In 30ème Congrès de l'Association des Pédiatres de Langue Française.
Peer reviewed

Verloes, A., Gillerot, Y., Walczak, E., Van Maldergem, L., & Koulischer, L. (15 January 1992). Acromelic Frontonasal "Dysplasia": Further Delineation of a Subtype with Brain Malformation and Polydactyly (Toriello Syndrome). American Journal of Medical Genetics, 42 (2), 180-3. doi:10.1002/ajmg.1320420209
Peer Reviewed verified by ORBi

Van Maldergem, L., Wetzburger, C., Verloes, A., Fourneau, C., & Gillerot, Y. (January 1992). Mental Retardation with Blepharo-Naso-Facial Abnormalities and Hand Malformations: A New Syndrome? Clinical Genetics, 41 (1), 22-4. doi:10.1111/j.1399-0004.1992.tb03622.x
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Lapiere, J. C., Verloes, A., Herens, C., Delfortrie, J., Van Maldergem, L., Gillerot, Y., & Koulischer, L. (1992). Combined 10pter-->P11 and 18pter-->Q11 Trisomy in a 7-Year-Old Child. Genetic Counseling, 3 (3), 155-9.
Peer Reviewed verified by ORBi

Koulischer, L., Schoos, R., Verloes, A., & Herens, C. (December 1991). Le dépistage prénatal de la trisomie 21 sur sérum maternel. Mise au point. Revue Médicale de Liège, 46 (12), 625-32.
Peer reviewed

Verloes, A., Schaaps, J.-P., Herens, C., Soyeur, D., Hustin, J., & Dodinval, P. (February 1991). Prenatal Diagnosis of Cystic Hygroma and Chorioangioma in the Wolf-Hirschhorn Syndrome. Prenatal Diagnosis, 11 (2), 129-32. doi:10.1002/pd.1970110209
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Verloes, A., Seret, N., Bernier, V., Gonzales, M., Herens, C., & Koulischer, L. (1991). Branchial Arch Anomalies in Trisomy 18. Annales de Génétique, 34 (1), 22-4.
Peer Reviewed verified by ORBi

Misson, J.-P., & Verloes, A. (1991). Familial neuronal heterotopias as cerebral palsy. An inherited disorder of brain histogenesis. In European Society of Human Genetics.
Peer reviewed

Verloes, A., Van Maldergem, L., de Marneffe, P., Dufier, J. L., & Maroteaux, P. (July 1990). Microspherophakia-Metaphyseal Dysplasia: A 'New' Dominantly Inherited Bone Dysplasia with Severe Eye Involvement. Journal of Medical Genetics, 27 (7), 467-71. doi:10.1136/jmg.27.7.467
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Herens, C., Verloes, A., Laloux, F., & Van Maldergem, L. (May 1990). Trisomy 20q. A New Case and Further Phenotypic Delineation. Clinical Genetics, 37 (5), 363-6. doi:10.1111/j.1399-0004.1990.tb03520.x
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Herens, C., Pierquin, G., Verloes, A., Schaaps, J.-P., & Frederic, J. (May 1989). Mosaicism of 46,Xx/47,Xx,+9/47,Xx,+?Mar in the Same Amniotic Fluid with Apparent Loss of One Cell Line after Delivery. Prenatal Diagnosis, 9 (5), 373-5. doi:10.1002/pd.1970090513
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Verloes, A., Herens, C., Van Maldergem, L., Retz, M. C., & Dodinval, P. (1989). Roberts-Sc Phocomelia Syndrome with Exencephaly. Annales de Génétique, 32 (3), 169-70.
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VERLOES, A., DRESSE, M.-F., Jovanovic, M., Dodinval, P., & Geubelle, F. (1989). 3C syndrome : third occurence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome). Clinical Genetics, 35 (3), 205-8.
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Verloes, A., Herens, C., Lambotte, C., & Frederic, J. (1987). Chromosome 22 Mosaic Monosomy (46,Xy/45,Xy,-22). Annales de Génétique, 30 (3), 178-9.
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